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Article

Changes in Health Behaviors, Mental and Physical Health among Older Adults under Severe Lockdown Restrictions during the COVID-19 Pandemic in Spain

by
Esther García-Esquinas
1,2,3,*,
Rosario Ortolá
1,2,3,
Iago Gine-Vázquez
4,5,
José A. Carnicero
6,7,
Asier Mañas
7,8,
Elvira Lara
5,9,10,
Alejandro Alvarez-Bustos
6,7,
German Vicente-Rodriguez
11,12,13,14,
Mercedes Sotos-Prieto
1,2,3,15,16,
Beatriz Olaya
4,5,
Francisco José Garcia-Garcia
7,17,
Narcis Gusi
7,18,
Jose R. Banegas
1,2,3,
Irene Rodríguez-Gómez
7,8,
Ellen A. Struijk
1,2,3,
David Martínez-Gómez
1,2,3,
Alberto Lana
19,
Josep María Haro
4,5,
José Luis Ayuso-Mateos
5,9,10,
Leocadio Rodríguez-Mañas
6,7,
Ignacio Ara
7,8,
Marta Miret
5,9,10 and
Fernando Rodríguez-Artalejo
1,2,3,16
add Show full author list remove Hide full author list
1
Department of Preventive Medicine and Public Health, School of Medicine, Universidad Autónoma de Madrid, 28029 Madrid, Spain
2
IdiPaz (Instituto de Investigación Sanitaria Hospital Universitario La Paz), 28029 Madrid, Spain
3
CIBERESP (CIBER of Epidemiology and Public Health), 28029 Madrid, Spain
4
Parc Sanitari Sant Joan de Déu, 08830 Sant Boi de Llobregat, Spain
5
CIBERSAM (CIBER of Mental Health), 28029 Madrid, Spain
6
Foundation for Biomedical Research, Getafe University Hospital, 28905 Getafe, Spain
7
CIBERFES (CIBER of Frailty and Healthy Aging), Instituto de Salud Carlos III, 28029 Madrid, Spain
8
GENUD Toledo Research Group, Universidad de Castilla-La Mancha, 45004 Toledo, Spain
9
Department of Psychiatry, School of Medicine, Universidad Autónoma de Madrid, 28029 Madrid, Spain
10
Department of Psychiatry, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Hospital Universitario de La Princesa, 28006 Madrid, Spain
11
GENUD (Growth, Exercise, Nutrition and Development) Research Group, Instituto Agroalimentario de Aragón IA2, Universidad de Zaragoza, 50013 Zaragoza, Spain
12
CIBEROBN (CIBER of Obesity and Nutrition), 28029 Madrid, Spain
13
Faculty of Health and Sport Science, University of Zaragoza, 22001 Huesca, Spain
14
Department of Physiatry and Nursing, University of Zaragoza, 22002 Aragón, Spain
15
Department of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA
16
IMDEA-Food Institute, CEI UAM+CSIC, 28049 Madrid, Spain
17
Hospital Virgen del Valle, Complejo Hospitalario de Toledo, 45071 Toledo, Spain
18
AFYCAV (Physical Activity, Quality of Life and Health) Research Group, Faculty of Sport Sciences, University of Extremadura, 10003 Cáceres, Spain
19
Department of Medicine, School of Medicine and Health Sciences, Universidad de Oviedo/ISPA, 33003 Oviedo, Spain
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2021, 18(13), 7067; https://doi.org/10.3390/ijerph18137067
Submission received: 3 June 2021 / Revised: 29 June 2021 / Accepted: 30 June 2021 / Published: 1 July 2021

Abstract

:
We used data from 3041 participants in four cohorts of community-dwelling individuals aged ≥65 years in Spain collected through a pre-pandemic face-to-face interview and a telephone interview conducted between weeks 7 to 15 after the beginning of the COVID-19 lockdown. On average, the confinement was not associated with a deterioration in lifestyle risk factors (smoking, alcohol intake, diet, or weight), except for a decreased physical activity and increased sedentary time, which reversed with the end of confinement. However, chronic pain worsened, and moderate declines in mental health, that did not seem to reverse after restrictions were lifted, were observed. Males, older adults with greater social isolation or greater feelings of loneliness, those with poorer housing conditions, as well as those with a higher prevalence of chronic morbidities were at increased risk of developing unhealthier lifestyles or mental health declines with confinement. On the other hand, previously having a greater adherence to the Mediterranean diet and doing more physical activity protected older adults from developing unhealthier lifestyles with confinement. If another lockdown were imposed during this or future pandemics, public health programs should specially address the needs of older individuals with male sex, greater social isolation, sub-optimal housing conditions, and chronic morbidities because of their greater vulnerability to the enacted movement restrictions.

1. Introduction

The COVID-19 pandemic has rocked our society to its core. Until safe and effective vaccines are globally distributed, social distancing interventions to reduce the transmission of SARS-CoV-2 are essential [1], but the interventions themselves are not exempt from health and economic challenges [2,3,4,5].
The State of Alarm imposed by the Spanish Government to curb the spread of the SARS-CoV-2 infection entailed a national lockdown starting on 15 March and the imposition of distancing measures such as the cancelation of mass events or the closure of non-essential customer-facing business and educational institutions [6].Two weeks later, on 29 March, the Government strengthened these measures to avoid the saturation of intensive care units [7]. A period of five weeks started in which citizens were only allowed to leave their homes for essential work, buying of staple products, or emergencies. On 4 May, citizens were first authorized to leave their homes to exercise or walk, for a maximum of 1 h a day, following timetables according to age and only being accompanied by people they had been living with during the lockdown. From 10 May to 21 June, a progressive de-escalation of confinement measures led to the so-called “New Normality”, in which Spaniards were allowed to attend their jobs, gather in small groups, and move between provinces as long as they complied with safe distancing and face covering requirements. All around the world, countries dealt with the first wave of the pandemic with different degrees of movement restrictions, but the Spanish lockdown, especially during those five weeks between 30 March and 4 May, was one of the most restrictive in Europe.
A few studies have investigated the health consequences of the lockdown during the first wave of the pandemic in the Spanish adult population. Using convenience sample surveys conducted between March and June 2020, in which participants reported their perceived changes in lifestyle and health-related factors since the start of the pandemic, these studies have shown a general worsening in psychological and mental health [8,9,10], as well as in sleep quality [11,12,13], mild or no changes in tobacco and alcohol consumption [11,14], slight or no changes in weight [14,15,16], conflicting results for diet quality [17,18], important reductions in physical activity, and increases in sedentary time [11,19,20,21]. Interestingly, one survey found that the percentage of interviewees meeting the guidelines regarding screen time became lower between 22 March and 5 April, while unhealthy alcohol consumption and insufficient physical activity decreased during this three-week period [22].
Unfortunately, none of these studies described the determinants of the observed changes in health behaviors, most were at high risk of information bias (i.e., people not accurately reporting their past exposures or symptoms, especially at a time of emotional distress), and, although a few provided stratified information by age groups, most presented aggregated information for young, middle-aged, and older adults. Moreover, most of these studies were based on convenience samples, which increase the risk of selection bias. As the COVID-19 epidemic evolves and new social distancing measures may be needed [23], and being aware of the risk of future infectious pandemics, it is critical that we identify population subgroups that are at increased risk of health deterioration with social isolation and confinement. This is especially important for older adults because they represent around 10% of the worldwide population (up to 20% in Spain), frequently live alone, and are most vulnerable to the development and progression of diseases including COVID-19.
In the general older adult population in Spain, the prevalence of tobacco smoking before the pandemic was very low, and about one-third of individuals reported consuming alcohol beverages (mostly wine) on a daily basis; adherence to the Mediterranean diet was much higher than in young and middle-age adults, but physical activity was much lower. Lastly, most older adults reported having good or only regular health, and in general reported better mental health than their young and middle-age counterparts. In this context, this study describes the main changes in health behaviors and in mental and physical health between a pre-pandemic period and weeks 7 to 15 after the beginning of the COVID-19 lockdown among participants in four cohorts of community-dwelling older adults in Spain [24].

2. Materials and Methods

2.1. Study Cohorts

Seniors-ENRICA-2 (ENRICA): Longitudinal study of older adults selected between 2015 and 2017 through sex- and district-stratified random sampling of all community-dwelling individuals aged ≥65 years holding a national healthcare card and living in the Madrid Region. In 2019 (baseline wave for the present study), participants were re-interviewed face-to-face at their homes using Computer-Assisted Personal Interviews (CAPI), and they underwent a physical exam and blood tests [25]. Participants gave informed written consent, and the Clinical Research Ethics Committee of the La Paz University Hospital in Madrid approved the study and its follow-ups (Protocol #HULP-PI 1793).
Edad con Salud (ES): Longitudinal population-based household survey representative of the non-institutionalized older adult population aged ≥60 years recruited in 206 municipalities in Spain. The first wave took place between 2011 and 2012 and was part of the Collaborative Research on Ageing in Europe (COURAGE) study. Participants were re-evaluated twice, between 2014 and 2015, and in 2018 [26]. In 2019–2020 (baseline wave for the present study), just before the start of the COVID-19 outbreak, a refreshment sample with participants from 9 municipalities in Barcelona and 7 municipalities in Madrid was added. Interviews were conducted face-to-face by trained lay interviewers at respondents’ homes using CAPI. The research protocol and its follow-ups were approved by the Clinical Research Ethics Review Committees of both Parc Sanitari Sant Joan de Déu (Barcelona, Spain) and Hospital Universitario La Princesa (Madrid, Spain). All participants provided written informed consent for their participation and the treatment of their personal data.
Toledo Study for Healthy Aging (TSHA): Prospective study of older adults aged ≥65 years recruited in 15 municipalities in the province of Toledo. The cohort was established between 2006 and 2009, and it had follow-up visits in 2011–2013 and 2016–2017 (baseline wave for the present study), when participants were interviewed at their homes using CAPI, underwent a physical exam, and provided blood and urine samples [27]. Participants gave informed written consent, and the Clinical Research Ethics Committee of Toledo Hospital Complex approved the study and subsequent follow-ups (Protocol # 2203/30/2005).
The elderly-Exernet multi-center study (EXERNET): Multi-center study of non-institutionalized individuals aged ≥65 years recruited in Aragón, Castilla-La Mancha, and Madrid. At baseline (2008–2009) and follow-up visits (2011–2012 and 2016–2017 (baseline wave for the present study)) participants responded to a face-to-face questionnaire and underwent a physical exam [28]. Participants gave informed written consent, and the Clinical Research Ethics Committee of Aragón approved the study and its follow-ups (#18/2008).

2.2. Study Participants

A total of 4936 participants from the cohorts with at least one pre-pandemic follow-up visit were eligible to participate in the study. From these, 753 individuals could not be contacted, and 717 did not agree to participate. After excluding 120 individuals infected with COVID-19, 97 living with a COVID-19 infected patient, as well as 208 participants with no information on important confounders, a total of 1323 individuals from ENRICA, 464 from ES, 829 from TSHA, and 425 from EXERNET comprised the analytical sample (n = 3041).

2.3. Study Variables

At baseline and at follow-up, we collected data on health behaviors, mental and physical health, and their potential determinants, including demographic and social variables, housing conditions, and aging experiences.

2.3.1. Baseline Information

Figure 1 shows the main variables collected at baseline in each cohort. In all cohorts, baseline information was collected on sociodemographic factors (sex, age, education, civil status); social isolation (cohabitation, frequency of contacts with family and friends); tobacco consumption; diet quality (14-point Mediterranean diet adherence screener questionnaire—MEDAS) [29]; physical activity, as per the EPIC-cohort questionnaire (EPAQ) [30] in ENRICA and the Elderly EXERNET Physical Activity Questionnaire (EEPAQ) [31] in EXERNET, with results expressed as Metabolic Equivalent Tasks (METs), the Global Physical Activity Questionnaire in ES [32], and the Physical Activity Scale for the Elderly (PASE) in the TSHA) [33]; measured weight and height, with the body mass index (BMI) being calculated as the weight in kg divided by squared height in m; hours of night-time sleep (short sleep defined as ≤6 h and long sleep as ≥9 h); quality of life (the 12-item Short Form (SF) in ENRICA [34], the WHO Disability Assessment Schedule 2.0 (WHODAS) in ES [35], and the EuroQol-5D [36] in TSHA and EXERNET); and history of physician-diagnosed chronic conditions (i.e., hypertension, diabetes, osteoarthritis, and depression). Definition of hypertension was based on a self-reported physician diagnosis, current use of anti-hypertensive medication, or a clinical blood pressure reading ≥140/90 mmHg. Type 2 diabetes mellitus was defined as a self-reported physician diagnosis, current use of anti-diabetic medication, or fasting glucose ≥126 mg/d.
Additionally, in some cohorts, information was collected on feelings of loneliness (the 3-item UCLA loneliness scale in ES, and a 0 to 5 scale in ENRICA) [37]; exposure to second-hand smoke (SHS) (ENRICA) [38]; alcohol intake (all cohorts but EXERNET); frequency of snack consumption and use of food to calm anxiety (ENRICA); time on sedentary activities (the Nurses’ Health Study questionnaire in ENRICA) [39] or overall sedentary time (ES and EXERNET); hours of day-time sleep (ENRICA and EXERNET); overall sleep quality (in all cohorts but TSHA); other indicators of poor night-time sleep quality (i.e., “difficulty falling asleep”, “awakening during night-time”, “early awakening with difficulty getting back to sleep” and “use of sleeping pills”) and drowsiness (i.e., “being so sleepy at day-time as to need a nap”, “not feeling rested in the morning”, and the Epworth Sleepiness Scale) in ENRICA [40]; prevalence and characteristics of pain (ENRICA) [41]; history of physician-diagnosed coronary heart disease, congestive heart failure, angina, or cancer at any site (all cohorts but EXERNET); mobility limitations, in ENRICA [42]; the Mini-Mental State Examination Score (MMSE) [43] (ENRICA and ES); the Cantril’s Ladder of Life Scale [44] (ENRICA and ES); and a negative aging experience scale that ranged from 1 (very positive experience) to 5 (very negative experience) (ENRICA).
Information on overall sleep quality was harmonized into a variable with the following categories: “very good”, “good”, “fair”, “poor/very poor”. Moreover, in ENRICA a 0 to 7 score with the number of poor sleep quality indicators was constructed as follows: those who answered “sometimes” or “almost always” to the items “difficulty falling asleep”, “awakening during night-time”, “early awakening with difficulty getting back to sleep”, “use of sleeping pills”, “being so sleepy at day-time as to need a nap”, or “not feeling rested in the morning”, as well as those with an Epworth Sleepiness Scale score > 10, received 1 point; their counterparts received 0 points. Additionally, in ENRICA, a pain scale ranging from 0 (no pain) to 7 (worse pain) was created based on pain frequency, intensity (assessed according to its impact on habitual activities), and number of pain sites. Sporadic (<2 times/week) and frequent (≥2 times/week) pain were assigned scores of 1 and 2, respectively; light, moderate, and high intensity pain, scores of 1, 2, and 3, respectively; and 1–2 and ≥3 pain sites scores of 1 and 2, respectively [41].

2.3.2. Follow-Up Information

Phone interviews were performed in the four cohorts between 27 April (week 7 of the pandemic) and 22 June (week 15), with information being collected on: presence and symptoms of COVID-19 cases within the household; number of outpatient or hospital health care visits during confinement; problems receiving health care or accessing medications during the pandemic; social isolation, degree of social support, and responsibilities towards dependents; sub-optimal housing conditions (including accessibility problems, noise annoyance, lack of internet access, absence of outdoor views or lack of a terrace/balcony or a private garden/yard to go out during confinement); tobacco consumption; passive tobacco smoke; alcohol drinking; diet quality; grocery modality during confinement (on-line, in-store) and person in charge; eating at a regular time (all cohorts but ES); eating more ultra-processed food than usual; eating snacks or food to calm anxiety (ENRICA); time spent in physical activities such as walking (i.e., to the supermarket, the pharmacy, or to walk the dog), exercising at home (i.e., with a stationary bike, a treadmill, fitness devices, etc.), engaging in do-it-yourself activities, or doing housework (ENRICA and EXERNET); the PASE questionnaire (TSHA and EXERNET); reasons for not doing any physical activity confinement; weight; time on sedentary activities (ENRICA) or overall sedentary time (EXERNET); hours of night-time sleep; hours of day-time sleep (ENRICA and EXERNET); poor sleep quality (all cohorts but the TSHA); quality of life (SF-12 in ENRICA and WHODAS in ES); frequency, intensity, and locations of pain (ENRICA).

2.4. Statistical Analysis

We first evaluated the longitudinal changes in the frequency of smoking, SHS, alcohol intake, diet, physical activity, measured weight, sedentary time, night-time and day-time sleep, sleep quality, overall health, and pain between the pre-confinement and confinement periods, by using mixed models with robust standard errors accounting for within-participant correlations induced by repeated measures. These mixed models were fitted with adjustment for sociodemographic, lifestyle, and health-related risk factors, including fixed effects for sex, educational level (primary or less, secondary, or university), baseline marital status (married, widowed, single, divorced), and study cohort (model 1); as well as fixed effects for baseline BMI and chronic morbidities, and changes over time in cohabitation status (living alone or not), smoking status (never, former or current), adherence to the Mediterranean diet score (0 to 14 points), physical activity (cohort-specific quartiles), night-time sleep, and overall health (cohort-specific quartiles) (model 2). To reduce the influence of increasing age during follow-up, we also conducted sensitivity analyses by excluding participants whose baseline measures were obtained earlier than 1.5 years before confinement.
In order to identify potential determinants of lifestyle changes or health decline during confinement, we then evaluated the relationship between baseline variables and changes in lifestyles and health outcomes. With this purpose, we used either linear or multinomial regression models that adjusted for baseline socio-demographic factors, housing conditions, smoking status, adherence to the Mediterranean diet, BMI, recreational activity and household activity, night-time sleep, chronic morbidities, time since last follow-up visit, cohort of study, and week of confinement. Although results from these models are given for each predictor and study outcome in tables, we tried to simplify the presentation of results by conducting additional backward stepwise linear and multinomial regression models with the studied baseline predictors (inclusion set at p < 0.1). These models were forced to adjust for age and sex, and their results are reported in figures, with red or blue colors identifying subjects with unhealthier and healthier changes, respectively. Categories “a” and “b” from multinomial regression models (defined in the paragraph below) represent these unhealthier (red) and healthier (blue) categories.
Linear (both fully adjusted and stepwise) regression was used to model the changes in the MEDAS score (all cohorts), weight (all cohorts), recreational and household activities (ENRICA and EXERNET), the PASE score (TSHA), total sedentary time (ENRICA and EXERNET), specific sedentary activities (ENRICA), hours of night-time sleep (all cohorts), number of total poor sleep quality indicators (ENRICA), physical component score (PCS) and mental component score (MCS) of the SF-12 (ENRICA), the WHODAS-12 (ES), and the pain scale (ENRICA). In addition, multinomial (both fully adjusted and stepwise) regression was used for the following a priori defined outcomes:
  • Changes in alcohol consumption. Participants in ENRICA, ES, and TSHA cohorts were classified into the following categories: (a) drinkers who increased their frequency of consumption (i.e., changed from not daily to daily drinkers); (b) drinkers who decreased their frequency of intake (i.e., changed from daily to not daily or to no consumption at all); (c) drinkers who did not change their frequency of consumption (reference); and (d) non-drinkers who maintained their non-drinking status during confinement.
  • Changes in diet quality. A “worsening” (a) and an “improvement” (b) categories were created including individuals who had either decreased or increased, respectively, their MEDAS score ≥ 1 point over follow-up; while a “reference” (c) category classified those who experienced no changes or slight increases/decreases (below 1 point) on this score.
  • Changes in weight. Individuals who gained or lost >1 kg were classified into an “increased weight” (a) or “decreased weight” (b) category, respectively, while those who experienced no or small (<1 kg) change in weight were classified into a “maintained weight” or “reference” (c) category.
  • Changes in physical activity and sedentary time. Participants in ENRICA, TSHA, and EXERNET cohorts were classified as experiencing: (a) “Unhealthier changes”, if they decreased physical activity or increased sedentary time more than the observed 75th percentile in each cohort; (b) “Healthier (than average or reference) changes”, if they decreased activity or increased sedentary time less than the 25th percentile or if they had slightly increased activity or decreased sedentary time with confinement; and (c) “Average” or “reference” changes if they changed between the 25th and 75th percentile.
  • Changes in night-time sleep. The following categories were defined: (a) “Worsening”, those who at baseline had normal sleep and developed short or long sleep with confinement; (b) “Improvement”, those who at baseline had short or long sleep and developed normal sleep during confinement; and (c) “Reference”, those who stayed in the same normal/non-normal sleep category.
  • Changes in sleep quality. Finally, older adults in ENRICA, ES, and EXERNET cohorts were classified into: (a) “Worsening”, if they had suffered an increase in the “poor sleep quality” score during confinement; (b) “Improvement”, if they decreased in that score; and (c) “Reference”, if they had no changes.
Statistical analyses were performed with Stata version 14.1 (StataCorp LP, College Station, TX, USA).

3. Results

Supplementary Table S1 shows the prevalence and mean (SD) estimates for the main sociodemographic, lifestyle, and health characteristics of participants in the four cohorts at the pre-confinement period (baseline) and the confinement follow-up period. At baseline, the mean age was 74.5 years and the proportion of men 42.3%, although this latter figure varied widely across cohorts (from 21.2% in EXERNET to 50.5% in ENRICA). The prevalence of university studies also differed across cohorts and ranged from >15% in the ENRICA and ES to 8% in TSHAA and EXERNET. Similarly, participants in ENRICA and ES showed a higher prevalence of Internet access. Overall, 65% of participants were married, 4% to 10% lived in houses with no outdoor views, and 24% to 37% lacked an outdoor terrace or balcony to go outside during confinement. Regarding social factors, the proportion of participants who lived alone was similar at baseline and during confinement (around 20–25% in all cohorts except for EXERNET, where the frequency was 35%). However, the percentage of participants without daily contact with family or friends halved during the pandemic. Moreover, in ENRICA, the single cohort where this information was available, no increases in lonely feelings during the study period were observed.

3.1. Changes in Tobacco Exposure, Alcohol Intake, Diet Quality, and Weight

Table 1 shows results for changes in the prevalence of smoking, SHS, alcohol intake, and diet quality between the pre-confinement and confinement periods. While the prevalence of active smoking remained stable, the likelihood of quitting smoking increased during follow-up. About half of the active smokers at confinement reported no changes in the frequency of tobacco consumption, while 22% reported an increase and 27% a decrease in the frequency of smoking since the start of the pandemic. The risk of increased consumption was higher among smokers with bad sleep quality at baseline and was lower among those lacking a terrace or balcony to smoke (Supplementary Table S2).
In ENRICA, the prevalence of SHS increased during follow-up, although this association was lost when excluding participants who had been followed-up for more than 1.5 years. The prevalence of current alcohol drinking was very similar in both periods, whereas a decreased likelihood of daily intake and a non-significant increased probability of daily intake were observed. Despite this change in the frequency of consumption, data from ENRICA showed that the prevalence of binge drinking (defined as having >5 units of alcohol in a session in men, or >4 in women) was lower during confinement (1.8%) than before (2.7%) (data not shown in tables). Among drinkers, only a few baseline factors were associated with the odds of changing the frequency of alcohol consumption; notably participants who lacked a terrace or balcony and former smokers showed a lower odds of increasing their frequency of alcohol intake during follow-up (Figure 2 and Supplementary Table S2).
The upper graph shows the odds ratios (95% confidence interval) of worsening (red color) or improving (blue color) alcohol intake according to the presence of the variables represented on the horizontal axis. Worsening was defined by increasing alcohol frequency from not daily to daily and improving as decreasing alcohol frequency from daily to not daily. For instance, the graph shows that participants who lacked a terrace or balcony and former smokers presented a lower odds of increasing their frequency of alcohol intake (worsening) during follow-up. The lower graph shows the same type of results for adherence to the Mediterranean diet. In this case, worsening and improving were defined by changes in the MEDAS score in one or more points during follow-up. Variables on the horizontal axis were selected with a backward stepwise regression from the list of candidate variables shown in Supplementary Tables S2 and S3.
Most study participants reported eating at a regular time during confinement, and a very low proportion declared eating more ultra-processed food than before (Supplementary Table S1). During confinement, 51.5% of study participants shopped face-to-face, 41.7% asked someone to shop for them, and 6.8% shopped online (data not shown in tables). In ENRICA, the odds of snacks consumption and that of use of food to calm anxiety was lower during the State of Alarm than in the pre-confinement period ((odds ratio (OR): 0.72; 95%CI: 0.60; 0.85) and (OR: 0.56; 95%CI: 0.41; 0.76)), respectively (Table 1), although the association with snacks consumption was lost when excluding participants whose follow-up was longer than 1.5 years. Data from all cohorts combined showed a mean reduction of 0.5 points (95%CI: −0.60; −0.45) in the MEDAS score during follow-up (Table 1). The items that were most negatively affected by the State of Alarm were fruits and vegetables, fish, wine, olive oil, and sofrito (a sauced made of olive oil and garlic); while the preference for olive oil and red meat, consumption of legumes, and consuming fewer sweets and cakes improved. Predictors of increased odds of worsening diet quality with confinement included having better MEDAS scores at baseline, being older, lacking outdoor views, and sleeping > 9 h/night (Figure 2 and Supplementary Table S3). A lower odds of worsening diet quality was observed for daily moderate drinkers and for individuals who performed more physical activity, while those with better general health and non-hypertensives were more likely to experience improvements in the MEDAS. No differences in changes in the MEDAS score were observed by grocery modality (data not shown).
Although 29% and 19% of participants reported “feeling they were getting fatter or thinner” with confinement, respectively, no changes in weight between study periods were observed in those with objective information (mean change: −0.57 kgs; 95%CI: −1.29; 0.15). Still, self-reported and objective information showed some correlation: on average, those who self-reported “feeling they were getting fatter” had gained 1.3 kg since the pre-confinement measure was taken, while those who self-reported “feeling they were losing weight” had lost, on average, −2.3 kg. Women, those with university studies, short night-time sleepers, and those who took longer naps at baseline experienced greater weight loss during follow-up than their counterparts (Supplementary Table S4).

3.2. Changes in Physical Activity and Sedentary Time

Physical activity and sedentary time were the lifestyle behaviors that changed the most with confinement (Table 1 and Supplementary Table S1). Compared with the pre-confinement period, participants in ENRICA and EXERNET showed a mean reduction in recreational and household physical activity of 17.48 METs h/week (95%CI: −18.61; −16.35) and 11.32 METs h/week (95%CI: −12.24; −10.41), respectively; participants in TSHA showed a mean reduction in the PASE score of 16.66 points (95%CI: −19.59; −13.73). Alleged reasons for not doing any physical activity during confinement among those who used to engage in some type of recreational activity before confinement included not being able to go outside (52.4%), not knowing how to perform physical activity at home (11.4%), not having the resources to do physical activity at home (13.3%), or not having enough time (3.4%). Only 3% of study participants increased their physical activity during confinement, and in general this was a slight increase (<4 METs h/week).
Regarding sedentary time, the ENRICA and EXERNET cohorts showed an average increase of 91.68 min/day (95%CI: 81.21; 102.11), which, according to the ENRICA, was more marked for active (i.e., time on the computer or tablet, time reading) than passive (i.e., television viewing) sedentary activities.
Interestingly, changes in physical activity and sedentary time seemed to reverse with time. Compared with those interviewed in the first weeks of total confinement, those interviewed when confinement measures started to be lifted showed a progressive increase in activity and a decrease in sedentary time: average changes per 1 further week of the State of Alarm were 1.45 METs h/week (95%CI: 0.24; 2.66) for recreational activity, −0.30 min/day (−0.44; −0.15) for sedentary time, and 8.83 points (95%CI: 4.31; 13.4) for the PASE score (Figure 3 and Supplementary Tables S5 and S6).
The upper graph shows the odds ratios (95% confidence interval) of decreasing physical activity more than the observed 75th percentile change (red color) or decreasing physical activity less than the observed 25th percentile change (blue color) according to the presence of the variables represented on the horizontal axis. For instance, the graph shows that females and those with greater adherence to the Mediterranean Diet (higher MEDAS scores) were more likely to decrease physical activity less than the observed 25th percentile change, while those with no daily contact with family or friends or with a lack of outdoor views were more likely to decrease physical activity more than the observed 75th percentile. Similarly, the lower graph shows the odds ratios (95% confidence interval) of increasing sedentary time more than the observed 75th percentile change (red color) or increasing sedentary time less than observed 25th percentile change (blue color) according to these variables. Variables on the horizontal axis were selected with a backward stepwise regression from the list of candidate variables shown in Supplementary Tables S5 and S6.
Compared with men, women showed higher odds of presenting healthier changes in activity (OR: 1.34; 95%CI: 1.03; 1.74) and sedentary time (OR: 1.54; 95%CI: 1.08; 2.19), as they seemed to compensate the inability to perform some recreational activities during confinement with increases in household activity, as well as higher reductions in TV viewing time (−0.31 min/day; 95%CI: −0.60; −0.02) and higher increases in reading time (0.19 min/day; 95%CI: 0.03; 0.45). In general, sub-optimal housing conditions such as not having outdoor views or lacking a garden/yard were associated with unhealthier changes in physical activity, as well as with higher increases in TV time with confinement, while not having internet access was associated with lower increases in sedentary time, particularly in screen time. Participants with higher baseline MEDAS scores were less likely to experience unhealthy changes in physical activity or sedentary time, while those who performed more activity were less likely to increase sitting time, and those who spent more time seated were less likely to reduce physical activity. Poor night-time sleep duration and day-time sleepiness at baseline were also associated with unhealthier changes in activity and sedentary time.

3.3. Changes in Sleep Duration and Sleep Quality

In multivariate models adjusted for changes in other potential confounders, data from all cohorts combined showed no changes in night-time sleep duration with confinement (−0.00 h/night; 95%CI: 0.06; 0.05). However, slight decreases were observed in day-time sleep duration (−12.08 min/day; 95%CI −13.73, −10.42) as well as in the “poor sleep quality” scale (0.12 points; 95%CI: 0.09; 0.15) (Table 1). Baseline predictors of unhealthier changes in sleep quality included being a married woman, living alone, feeling lonelier, doing more physical activity, a lower adherence to the Mediterranean diet, having worse overall health, and greater pain (Supplementary Table S7 and Figure 4).
The upper graph shows the odds ratios (95% confidence interval) of worsening (red color) or improving (blue color) sleep quality. Variables on the horizontal axis were selected with a backward stepwise regression from the list of candidate variables shown in Supplementary Tables S5 and S6.

3.4. Changes in Physical and Mental Health and Pain

During confinement, 23% and 4.9% of study participants attended a primary health center or an emergency room for reasons not related to a COVID-19 infection. Most of them (87.4% and 91.2%, respectively) declared they were satisfied with the care received. Most participants took their usual medication, although a few (n = 4) declared not being able to get medications because of the imposed mobility restrictions (data not shown in tables).
In multivariate analyses, participants in ENRICA showed a mean increase of 4.79 points (95%CI: 4.72; 5.38) in the PCS of the SF-12, a reduction of 1.19 points (95%CI: −1.81; –0.58) in the MCS of the SF-12, and an increase of 0.18 points (95%CI: 0.05–0.30) in the pain scale (Table 1), while the participants in the ES study showed a non-significant 0.18-point decrease (95%CI: −1.85; 1.48) in the WHODAS score. Table 2 shows the main predictors of health decline during confinement. Interestingly, the positive changes in the PCS reverted when participants returned to their normal activities (mean changes in the PCS per week of the State of Alarm: −0.64; 95%CI: −1.07; −0.20), while the effects on mental health (mean changes per week of State of Alarm: 0.99; 95%CI: 0.52; 1.46) and pain (0.10; 95%CI: 0.00; 0.20) showed a stronger magnitude in those interviewed later in time. As shown in Table 2, older adults experienced unhealthier changes in the PCS (mean changes per year increase: −0.19; 95%CI: −0.29; −0.08) and the WHODAS-12 (mean changes per year increase: 0.14; 95%CI: −0.05; 0.33) but experienced healthier changes in the MCS (mean changes per year increase: 0.12; 95%CI: 0.00; 0.23). Women in ENRICA showed greater deterioration in mental health (mean changes in MCS: −2.46; 95%CI: −3.65; −1.35) and pain (mean changes in pain score: 0.28; 95%CI:0.03; 0.51), while participants with higher education in the ES study showed healthier changes in the WHODAS-12 (mean change −4.12; 95%CI: −7.70; −0.53) than their counterparts.
Other predictors of unhealthier changes in the PCS were lacking a garden/yard, poorer sleep quality, hypertension, cardiovascular disease, cancer, depression, mobility limitations, and lower general life satisfaction. Predictors of unhealthier changes in MCS were living alone, feeling lonelier, having too much noise at home, doing less physical activity, taking very long naps, having mobility limitations, a negative aging experience, and low MMSE scores. Finally, unhealthier changes in pain were observed in participants who lived in homes with more noise, as well as in those who suffered from baseline short sleep, worse overall health, osteo-muscular disease, depression, mobility limitations, or lower general life satisfaction.

3.5. Sensitivity Analyses

When analyses were restricted to the 857 participants whose baseline measurements had been taken as far apart as 1.5 years before the State of Alarm, consistent findings were observed for most variables except for SHS, snacks consumption, and household physical activity, which no longer showed significant changes. The relationship with changes in some MEDAS items (i.e., vegetables, red meat, wine, sweets and cakes) also disappeared, and a slight decrease in night-time sleep was now observed (mean change −0.16 h/day; 95%CI: −0.27; −0.06).

4. Discussion

This study, conducted with older adults from four Spanish population-based cohorts, showed that, on average, strict confinement was not associated with a deterioration in lifestyle risk factors, except for physical activity and sedentary time, whose effects seemed to reverse with the end of the State of Alarm. Despite this, results from the ENRICA suggested moderate declines in mental health that did not seem to reverse after restrictions were lifted. On the other hand, the apparent improvements in physical health in participants from this last cohort did reverse with the end of the State of Alarm and may have been related to a better self-perceived performance at a less physically demanding time.
This study identified subgroups of individuals at increased risk of developing unhealthier lifestyles with confinement, including males (for physical activity and sedentariness), those without daily contact with family and friends (for diet and physical activity), married participants (for sleep quality), those with feelings of loneliness (for diet and sleep quality), those with sub-optimal housing conditions (for diet, physical activity, TV viewing time), those with unhealthy sleep duration, as well as those with worse overall health or chronic morbidities (i.e., subjects with obesity or diabetics suffered greater reductions in physical activity and greater increases in screen time). On the other hand, having a greater adherence to the Mediterranean diet and doing more physical activity protected older adults from developing unhealthier lifestyles with confinement.
What do other studies say about changes in smoking, alcohol intake, diet quality, and weight during the COVID-19 pandemic?
Different on-line surveys conducted during the first months of the pandemic in adults from China [45], France [46], the Netherlands [47], or the United Kingdom [48] have shown that current smokers were similarly likely (around 20–25%) to increase or decrease their tobacco consumption with the pandemic. In the Dutch survey, authors found that this apparently contradictory relationship was driven both by a negative effect of stress, boredom, and restriction on smoking and by a positive effect of motivation to quit smoking from fear of contracting COVID-19 and becoming severely ill. Consistently, in a Chinese survey, participants with higher epidemiologic concern were more often willing to improve their diets [49]. In the UK study, on the other hand, symptoms of mental distress (i.e., anxiety, low mood, sleeping problems) during quarantine were more frequently associated with increasing than decreasing tobacco smoke. Although in secondary analysis we did not find a relationship between symptoms of psychological distress and depression (measured at follow-up with the General Health Questionnaire-12 [50] and the Geriatric Depression Scale [51]) and changes in smoking frequency, we did observe that smoking older adults who spent more time listening or reading news related to the COVID-19 outbreak were more likely to increase their tobacco consumption (data not shown in tables). Our study provides evidence that smokers with poor sleep quality may be at higher risk of increasing smoking frequency in stressful situations than those who have good sleep quality. It also shows that while “lacking a terrace or balcony” was positively associated with unhealthier changes in physical activity and sedentary time with confinement, it reduced the risk of smokers and drinkers to increase their frequency of tobacco and alcohol intake, respectively.
In our study, the proportion of alcohol drinkers who increased and that of those who decreased alcohol intake with lockdown was very similar, around 15%. Compared with other surveys, the frequency of increased alcohol consumption was much lower in our population than in adults in Germany (34.7%) [52], Australia (20.0% [53] to 30.8% [54]), or the USA (29%) [55] and was more similar to that reported in other Spanish [14,22], French [46,56], and Italian surveys [57]. In fact, in these studies, declining alcohol consumption during quarantine was more common than increasing it. Although some of the observed differences across countries may be accounted for by discrepancies in study designs (pre-post comparisons vs online surveys) and age of participants, they may also be influenced by the more social nature of drinking in Southern European countries than in other cultures. In any case, to our knowledge, ours are the first results that are entirely based on an elderly population.
Results for changes in diet quality are difficult to compare because of differences in diet assessment across studies, with some showing the proportion of those who increased or decreased the consumption of certain products [11,15,57,58], others asking participants to report their self-perceived changes in quality [56,59], and only a few studies providing validated diet quality scores [17,18,60]. Even for the latter, comparisons are limited due to the use of different scales; for instance, in a Spanish study, confinement was associated with a mean increase of 0.8 points in the MEDAS score [17], in one French study it was associated with a mean reduction of 0.32 points in the simplified PNNS-GS2 index [18], while in another study it was associated with equivalent increases or decreases in the Alternative Healthy Eating Index [60]. Other factors compounding this comparison are the retrospective collection of pre-confinement information and the lack of focus on older adults.
Our results were somewhat expected because, during the State of Alarm, both older adults (the segment of the population that is more used to daily shopping for foodstuffs in Spain [61]) and the whole the population inevitably had to decrease the frequency of shopping for foods that are typically consumed fresh (i.e., fruits, vegetables, or fish). In line with our results, two Spanish surveys indicated a reduction in the consumption of these fresh foods in younger adults during confinement [17,22]. Despite this, we observed some compensations in diet quality in older adults thanks to a decrease in the intake of foods not typical in the Mediterranean diet (i.e., red meat, sweets and cakes), or an increase in the consumption of legumes, which are typically prepared at home.
Previous surveys described mental health during confinement as an important predictor of reductions in diet quality, a fact confirmed in our study, where those with higher follow-up GDS-10 scores showed a higher risk of diet quality decline (relative risk ratio (RRR) per 1 point increase in the GDS-10: 1.25; 95%CI: 1.13–1.39). We also identified a number of baseline predictors of diet decline with confinement: social isolation (which may reflect not having someone to buy fresh foods for them), a lack of outdoor views (which is associated with lower income), the insufficiency of physical activity, or suffering with poor general health or hypertension.
Changes in weight occurring in short periods of time may be important if, as the literature on obesity suggests, they remain over time [62]. Fortunately, though, most surveys either showed no or small changes in weight with confinement [14,15,16]. In our study, despite mean declines in diet quality and physical activity, only specific subgroups of older adults (mainly hypertensives and those with a negative aging experience) presented significant weight gains. Moreover, we observed that women, those with university studies, and those with short sleep and very long naps presented significant weight loss. The fact that weight loss was not associated with either baseline or follow-up (secondary analysis) overall health, psychological distress, or depression symptoms reduces the probability that it was involuntary, and thus indicative of an increased risk of frailty [63]. In any case, underlying changes in body composition (i.e., reduction in muscle mass and increase in fat mass) associated with the COVID-19 lockdown deserve further study in the older population.
What do other studies say about changes in physical activity and sedentary time during the COVID-19 pandemic?
Surveys on non-institutionalized adults have shown declines in physical activity and increases in sedentary time with confinement, which varied according to varying degrees and lengths of lockdown [11,19,20,64,65,66], with unhealthier changes generally observed among those with higher activity and lower sedentariness at baseline [19,64,66] and among those who had follow-up symptoms of loneliness and worse mental health [12,19,64,66]. In our study, we corroborated the association between previous levels of activity and sedentariness and changes in these behaviors with confinement, probably reflecting the regression to the mean phenomenon. Additionally, we first identified subpopulations of older adults who may be at increased risk of decreasing PA or increasing ST during quarantine. This information can help prioritize subgroups for health promotion or for being allowed to go outside, should future home confinements take place (i.e., the oldest old, those with worse housing conditions, or individuals with diabetes).
What do other studies say about changes in sleep duration and sleep quality during the COVID-19 pandemic?
Worse sleep quality with confinement has been reported among the adult general population in different countries [11,12,13,66], and it is partly attributed to inactivity [12] and higher anxiety and mental distress during isolation [21]. In our study, the association with mental health during quarantine was confirmed, with an increased risk of reducing sleep quality in individuals with higher GDS-10 scores (RRR: 1.25; 95%CI: 1.13–1.39; data not shown in tables). Moreover, our study identified for the first time predictors of these changes, showing that older women who live alone and feel lonely, those with worse diet quality, as well as those with worse overall health and higher pain are at increased risk of developing sleep problems with confinement.
What do other studies say about changes in overall health and pain during the COVID-19 pandemic?
A quantity of evidence supports a link between confinement and decline in mental health, both in middle-aged and older adults, and provides evidence that female gender [9] and being younger [67] are risk factors of these declines. However, we have only found one study evaluating the effect of confinement on chronic pain, which showed a mild improvement of migraine features during quarantine [68]. Now we have identified subgroups of older adults who are more vulnerable to mental health decline with confinement, including those who feel lonelier, perform less physical activity, have mobility limitations, low MMSE scores, or a negative aging experience. In addition, we found that individuals who lacked a garden/yard or who had poor sleep quality, hypertension, cardiovascular disease, cancer, depression, or mobility limitations were at increased risk of deteriorating physical function during confinement. Finally, we observed that women with short sleep, worse overall health, and lower overall life satisfaction, osteo-muscular disease, and depression, as well as those who suffered from mobility limitations were at increased risk of pain worsening.

Study Limitations and Strengths

Among the limitations of the present study are that not all cohorts had information in all of the studied variables and that there was a lack of data on the longer-term (July–December) effects of isolation measures. Moreover, the study cohort did not include institutionalized older adults, so results may not be generalizable to them. However, ours is one of the very few studies that have evaluated the effects of the pandemic in non-COVID-19-infected community dwelling older adults. Moreover, unlike most of the reviewed web-based surveys, it relied on telephone interviews and used pre-pandemic in-home collected information on participants’ health behaviors and health status, reducing the risk of information bias (i.e., people not accurately reporting their past exposures or symptoms).

5. Conclusions

The lockdown during the first wave of COVID-19 in Spain, which was one of the most restrictive in Europe, was not associated with a deterioration in lifestyle risk factors (smoking, alcohol intake, diet, or weight), except for decreased physical activity and increased sedentary time, which reversed with the end of confinement. However, mental health was affected, particularly in those living alone, feeling lonelier, with mobility limitations, and with lower cognitive function. If another lockdown is imposed in this or in future pandemics, public health programs should specially address the needs of older individuals of male sex, with greater social isolation, sub-optimal housing conditions, and chronic morbidities because of their greater vulnerability to the enacted movement restrictions.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/ijerph18137067/s1, Table S1: Prevalence or mean (SD) for the main sociodemographic, lifestyle and health-related characteristics of older adults at the COVID-19 pre-confinement period (t0) and the State of Alarm (t1), Table S2: Prospective association between baseline participant characteristics and changes in frequency of tobacco (n = 194: 93 from Seniors ENRICA-2, 67 from Edad con Salud, 31 from TSHA, and 3 from Exernet) and alcohol (n = 2616: 1323 from Seniors ENRICA-2, 464 from Edad con Salud, and 829 from TSHA) consumption between the COVID-19 pre-confinement period and the State of Alarm, Table S3: Prospective association between participant characteristics at baseline and changes in adherence to the MEDAS score between the COVID-19 pre-confinement period and the State of Alarm (n = 3041: 1323 from Seniors ENRICA-2, 464 from Edad con Salud, 829 from TSHA, and 425 from EXERNET), Table S4: Prospective association between participant characteristics at baseline and changes in weight between the COVID-19 pre-confinement period and the State of Alarm (n = 1561: 792 from Seniors-ENRICA-2, 239 from Edad con Salud, 312 from TSHA and 218 from Exernet), Table S5: Prospective association between participant characteristics and changes in overall physical activity (n = 2577: 1323 from Seniors ENRICA-2, 829 from TSHA, and 425 from EXERNET), recreational physical and household physical activity (n = 1748: 1323 from Seniors ENRICA-2 and 425 from EXERNET), and the PASE score (n = 829 from TSHA) between the COVID-19 pre-confinement period and the State of Alarm, Table S6: Prospective association between participant characteristics at baseline and changes in overall sedentary time (n = 1746: 1321 from Seniors-ENRICA-2 and 425 from Exernet), as well as in specific sedentary activities (n = 1270 for TV viewing, 1196 for other screen time and 1297 for reading time in participants from the Seniors-ENRICA-2) between the COVID-19 pre-confinement period and the State of Alarm, Table S7: 7 Prospective association between participant characteristics and changes in night-time sleep (n = 2867, 1294 from Seniors-ENRICA-2, 411 from Edad con Salud, 763 from TSHA and 399 from Exernet), sleep quality (n = 2095; 1289 from Seniors-ENRICA-2, 430 from Edad con Salud, and 376 from Exernet), and nº of poor sleep quality indicators (n = 1285 in Seniors-ENRICA 2) during the COVID-19 confinement.

Author Contributions

E.G.-E., J.M.H., J.L.A.-M., L.R.-M., I.A., M.M., and F.R.-A. conceptualized the study. E.G.-E., R.O., I.G.-V., J.A.C., and A.M. conducted statistical analyses. E.G.-E. and F.R.-A. interpreted the results and drafted the initial manuscript. E.G.-E., R.O., I.G.-V., J.A.C., A.M., E.L., A.A.-B., G.V.-R., M.S.-P., B.O., F.J.G.-G., N.G., J.R.B., I.R.-G., E.A.S., D.M.-G., A.L., J.M.H., J.L.A.-M., L.R.-M., I.A., M.M., F.R.-A. reviewed the manuscript for important intellectual content and approved the final version as submitted. All authors have read and agreed to the published version of the manuscript.

Funding

The Seniors-ENRICA-2 study was supported by Instituto de Salud Carlos III (Spain), State Secretary of R+D+I and FEDER/FSE research grants PI16/609, PI18/287, and 19/319; CIBERESP (16/01); and Cátedra de Epidemiología y Control del Riesgo Cardiovascular at UAM (#820024). ELS was supported by a Juan de la Cierva Contract from the Ministy of Universities. DMG and MSP were supported by supported by a “Ramon y Cajal”contract. Edad con Salud was funded by the Seventh Framework Programme (grant number 223071-COURAGE Study); the Instituto de Salud Carlos III (grants number PS09/00295(JMH), PS09/01845 (JLA), PI12/01490 (JMH), PI13/00059 (JLA), PI16/00212 (JMH), PI16/00218 (MM), PI16/01073 (JLA)); the European Regional Development Fund (ERDF) “A Way to Build Europe” (grant numbers PI12/01490, PI13/00059, PI16/00212 and PI16/01073);and CIBERSAM. EL was supported by the Sara Borrell postdoctoral programme (CD18/00099) from the Instituto de Salud Carlos III and co-funded by the European Union (FEDER/FSE, “Investing in your future”). BO was supported by the Miguel Servet programme (reference CP20/00040), funded by Instituto de Salud Carlos III and co-funded by European Union (ERDF/ESF, "Investing in your future"). The Toledo Study for Healthy Ageing was funded by the Spanish Ministry of Economy, Industry and Competitiveness, cofinanced by FEDER (RD120001/0043), CIBERFES (CB16/10/00464) and DIABFRAIL-LATAM (contract number 825546, Horizon 2020). The Elderly EXERNET multicenter study was supported by the Ministerio de Economía, Industria y Competitividad (DEP2016-78309-R (GVR)), the Ministerio de Educación y Ciencia (Red EXERNET DEP2005-00046 JAC)), the High Council of Sports (Consejo Superior de Deportes) of the Ministerio de Cultura y Deportes (09/UPB/19 (JAC) and 45/UPB/20 (JAC)), CIBERFES, the 4IE+ project (0499_4IE_PLUS_4_E (NG)) funded by the Interreg V-A España-Portugal (POCTEP) 2014-2020 program, and FEDER funds from the European Union (CB16/10/00477 (IA)). The funding agencies had no role in study design, data collection and analysis, interpretation of results, manuscript preparation or the decision to submit this manuscript for publication.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and was approved by the Institutional Review Boards of La Paz University Hospital in Madrid, Parc Sanitari Sant Joan de Déu in Barcelona, La Princesa Hospital in Madrid, Toledo Hospital Complex in Madrid, and the Clinical Research Ethics Committee of Aragón.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Data are available on the study cohorts upon request.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Pan, A.; Liu, L.; Wang, C.; Guo, H.; Hao, X.; Wang, Q.; Huang, J.; He, N.; Yu, H.; Lin, X.; et al. Association of Public Health Interventions with the Epidemiology of the COVID-19 Outbreak in Wuhan, China. JAMA 2020, 323, 1915. [Google Scholar] [CrossRef] [Green Version]
  2. International Monetary Fund. World Economic Outlook, October 2020: A Long and Difficult Ascent; International Monetary Fund: Washington, DC, USA, 2020. [Google Scholar]
  3. Niedzwiedz, C.L.; Green, M.J.; Benzeval, M.; Campbell, D.; Craig, P.; Demou, E.; Leyland, A.; Pearce, A.; Thomson, R.; Whitley, E.; et al. Mental health and health behaviours before and during the initial phase of the COVID-19 lockdown: Longitudinal analyses of the UK Household Longitudinal Study. J. Epidemiol. Community Health 2020, 75, 224–231. [Google Scholar] [CrossRef] [PubMed]
  4. Fiorillo, A.; Sampogna, G.; Giallonardo, V.; Del Vecchio, V.; Luciano, M.; Albert, U.; Carmassi, C.; Carrà, G.; Cirulli, F.; Dell’Osso, B.; et al. Effects of the lockdown on the mental health of the general population during the COVID-19 pandemic in Italy: Results from the COMET collaborative network. Eur. Psychiatry 2020, 63, 1–28. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Beck, F.; Léger, D.; Fressard, L.; Peretti-Watel, P.; Verger, P. The Coconel Group Covid-19 health crisis and lockdown associated with high level of sleep complaints and hypnotic uptake at the population level. J. Sleep Res. 2021, 30, e13119. [Google Scholar] [CrossRef]
  6. Real Decreto 463/2020, de 14 de Marzo, Por el Que se Declara el Estado de Alarma para la Gestión de la Situación de Crisis Sanitaria Ocasionada por el COVID-19. Available online: https://www.boe.es/buscar/doc.php?id=BOE-A-2020-3692 (accessed on 1 July 2021).
  7. Real Decreto 10/2020, de 29 de Marzo, Por el Que se Regula un Permiso Retribuido Recuperable para las Personas Trabaja-Doras por Cuenta Ajena Que No Presten Servicios Esenciales, Con el Fin de Reducir la Movilidad de la Población en el Con-Texto de la Lucha Contra El COVID-19. Available online: https://www.boe.es/buscar/doc.php?id=BOE-A-2020-4166 (accessed on 1 July 2021).
  8. Justo-Alonso, A.; García-Dantas, A.; González-Vázquez, A.I.; Sánchez-Martín, M.; Del Río-Casanova, L. How did Different Generations Cope with the COVID-19 Pandemic? Early Stages of the Pandemic in Spain. Psicothema 2020, 32, 490–500. [Google Scholar]
  9. González-Sanguino, C.; Ausín, B.; Castellanos, M.Á.; Saiz, J.; López-Gómez, A.; Ugidos, C.; Muñoz, M. Mental health consequences during the initial stage of the 2020 Coronavirus pandemic (COVID-19) in Spain. Brain Behav. Immun. 2020, 87, 172–176. [Google Scholar] [CrossRef]
  10. Pérez, S.; Masegoso, A.; Hernández-Espeso, N. Levels and variables associated with psychological distress during confinement due to the coronavirus pandemic in a community sample of Spanish adults. Clin. Psychol. Psychother. 2020. [Google Scholar] [CrossRef]
  11. Balanzá-Martínez, V.; Kapczinski, F.; Cardoso, T.D.A.; Atienza-Carbonell, B.; Rosa, A.R.; Mota, J.C.; De Boni, R.B. The assessment of lifestyle changes during the COVID-19 pandemic using a multidimensional scale. Rev. Psiquiatr. Salud Ment. 2021, 14, 16–26. [Google Scholar] [CrossRef] [PubMed]
  12. Werneck, A.O.; Silva, D.R.; Malta, D.C.; Lima, M.G.; Souza-Júnior, P.R.; Azevedo, L.O.; Barros, M.B.; Szwarcwald, C.L. The mediation role of sleep quality in the association between the incidence of unhealthy movement behaviors during the COVID-19 quarantine and mental health. Sleep Med. 2020, 76, 10–15. [Google Scholar] [CrossRef] [PubMed]
  13. Robillard, R.; Dion, K.; Pennestri, M.; Solomonova, E.; Lee, E.; Saad, M.; Murkar, A.; Godbout, R.; Edwards, J.D.; Quilty, L.; et al. Profiles of sleep changes during the COVID-19 pandemic: Demographic, behavioural and psychological factors. J. Sleep Res. 2021, 30, e13231. [Google Scholar] [CrossRef] [PubMed]
  14. López-Moreno, M.; López, M.T.I.; Miguel, M.; Garcés-Rimón, M. Physical and Psychological Effects Related to Food Habits and Lifestyle Changes Derived from Covid-19 Home Confinement in the Spanish Population. Nutrients 2020, 12, 3445. [Google Scholar] [CrossRef]
  15. López, J.M.M.; Loaiza, L.I.S.; Belda, B.V.; Cepeda, A.; Cobas, A.C. Food habits in the Galician population during confinement for COVID-19. Nutr. Hosp. 2020, 37, 1190–1196. [Google Scholar] [CrossRef]
  16. Fernandez-Rio, J.; Cecchini, J.A.; Mendez-Gimenez, A.; Carriedo, A. Weight changes during the COVID-19 home confinement. Effects on psychosocial variables. Obes. Res. Clin. Pract. 2020, 14, 383–385. [Google Scholar] [CrossRef] [PubMed]
  17. Rodríguez-Pérez, C.; Molina-Montes, E.; Verardo, V.; Artacho, R.; García-Villanova, B.; Guerra-Hernández, E.J.; Ruíz-López, M.D. Changes in Dietary Behaviours during the COVID-19 Outbreak Confinement in the Spanish COVIDiet Study. Nutrients 2020, 12, 1730. [Google Scholar] [CrossRef] [PubMed]
  18. Marty, L.; de Lauzon-Guillain, B.; Labesse, M.; Nicklaus, S. Food choice motives and the nutritional quality of diet during the COVID-19 lockdown in France. Appetite 2021, 157, 105005. [Google Scholar] [CrossRef] [PubMed]
  19. Castañeda-Babarro, A.; Arbillaga-Etxarri, A.; Gutiérrez-Santamaría, B.; Coca, A. Physical Activity Change during COVID-19 Confinement. Int. J. Environ. Res. Public Health 2020, 17, 6878. [Google Scholar] [CrossRef] [PubMed]
  20. García-Tascón, M.; Sahelices-Pinto, C.; Mendaña-Cuervo, C.; Magaz-González, A.M. The Impact of the COVID-19 Confinement on the Habits of PA Practice According to Gender (Male/Female): Spanish Case. Int. J. Environ. Res. Public Health 2020, 17, 6961. [Google Scholar] [CrossRef]
  21. Stanton, R.; To, Q.G.; Khalesi, S.; Williams, S.L.; Alley, S.J.; Thwaite, T.L.; Fenning, A.S.; Vandelanotte, C. Depression, Anxiety and stress during COVID-19: Associations with changes in physical activity, sleep, tobacco and alcohol use in australian adults. Int. J. Environ. Res. Public Health 2020, 17, 4065. [Google Scholar] [CrossRef]
  22. López-Bueno, R.; Calatayud, J.; Casaña, J.; Casajús, J.A.; Smith, L.; Tully, M.A.; Andersen, L.L.; López-Sánchez, G.F. COVID-19 Confinement and Health Risk Behaviors in Spain. Front. Psychol. 2020, 11, 1426. [Google Scholar] [CrossRef]
  23. Real Decreto 900/2020, de 9 de Octubre, por el Que se Declara el Estado de Alarma para Responder Ante Situaciones de Es-Pecial Riesgo por Transmisión no Controlada de Infecciones Causadas por el SARS-CoV-2. Available online: https://www.boe.es/buscar/act.php?id=BOE-A-2020-12109 (accessed on 1 July 2021).
  24. National Health Interview Survey, Spain; Ministry of Health. 2017. Available online: https://www.mscbs.gob.es/estadEstudios/estadisticas/encuestaNacional/encuestaNac2017/encuestaResDetall2017.htm (accessed on 1 July 2021).
  25. García-Esquinas, E.; Carrasco-Rios, M.; Ortolá, R.; Prieto, M.S.; Pérez-Gómez, B.; Gutiérrez-González, E.; Banegas, J.; Queipo, R.; Olmedo, P.; Gil, F.; et al. Selenium and impaired physical function in US and Spanish older adults. Redox Biol. 2021, 38, 101819. [Google Scholar] [CrossRef]
  26. Olaya, B.; Moneta, M.V.; Lara, E.; Miret, M.; Martín-María, N.; Moreno-Agostino, D.; Ayuso-Mateos, J.L.; Abduljabbar, A.S.; Haro, J.M.; Essau, C.A.; et al. Fruit and Vegetable Consumption and Potential Moderators Associated with All-Cause Mortality in a Representative Sample of Spanish Older Adults. Nutrients 2019, 11, 1794. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Garcia-Garcia, F.J.; Avila, G.G.; Alfaro-Acha, A.; Andres, M.S.A.; Lanza, M.D.L.A.D.L.T.; Aparicio, M.V.E.; Aparicio, S.H.; Zugasti, J.L.L.; Reus, M.G.-S.; Rodriguez-Artalejo, F.; et al. The prevalence of frailty syndrome in an older population from Spain. The Toledo study for healthy aging. J. Nutr. Health Aging 2011, 15, 852–856. [Google Scholar] [CrossRef] [PubMed]
  28. Gomez-Bruton, A.; Navarrete-Villanueva, D.; Pérez-Gómez, J.; Vila-Maldonado, S.; Gesteiro, E.; Gusi, N.; Villa-Vicente, J.G.; Espino, L.; Gonzalez-Gross, M.; Casajus, J.A.; et al. The effects of Age, Organized Physical Activity and Sedentarism on Fitness in Older Adults: An 8-Year Longitudinal Study. Int. J. Environ. Res. Public Health 2020, 17, 4312. [Google Scholar] [CrossRef] [PubMed]
  29. Schröder, H.; Fitó, M.; Estruch, R.; Martínez-González, M.A.; Corella, D.; Salas-Salvadó, J.; Lamuela-Raventós, R.; Ros, E.; Salaverría, I.; Fiol, M.; et al. A Short Screener Is Valid for Assessing Mediterranean Diet Adherence among Older Spanish Men and Women. J. Nutr. 2011, 141, 1140–1145. [Google Scholar] [CrossRef] [Green Version]
  30. Pols, M.A.; Peeters, P.H.; Ocké, M.C.; Slimani, N.; Bueno-De-Mesquita, H.B.; Collette, H.J. Estimation of reproducibility and relative validity of the questions included in the EPIC Physical Activity Questionnaire. Int. J. Epidemiol. 1997, 26, S181–S189. [Google Scholar] [CrossRef] [Green Version]
  31. López-Rodríguez, C.; Laguna, M.; Gómez-Cabello, A.; Gusi, N.; Espino, L.; Villa, G.; Pedrero-Chamizo, R.; Casajus, J.; Ara, I.; Aznar, S. Validation of the self-report EXERNET questionnaire for measuring physical activity and sedentary behavior in elderly. Arch. Gerontol. Geriatr. 2017, 69, 156–161. [Google Scholar] [CrossRef]
  32. Craig, C.L.; Marshall, A.L.; Sjöström, M.; Bauman, A.E.; Booth, M.L.; Ainsworth, B.E.; Pratt, M.; Ekelund, U.; Yngve, A.; Sallis, J.F.; et al. International Physical Activity Questionnaire: 12-Country Reliability and Validity. Med. Sci. Sports Exerc. 2003, 35, 1381–1395. [Google Scholar] [CrossRef] [Green Version]
  33. Logan, S.L.; Gottlieb, B.H.; Maitland, S.B.; Meegan, D.; Spriet, L.L. The Physical Activity Scale for the Elderly (PASE) Questionnaire; Does It Predict Physical Health? Int. J. Environ. Res. Public Health 2013, 10, 3967–3986. [Google Scholar] [CrossRef]
  34. Ware, J.E.; Kosinski, M.; Turner-Bowker, D.M.; Gandek, B. How to Score Version 2 of the Sf-12 Health Survey (with a Supplement Documenting Version 1); Quality Metric Inc. Health Assessment Laboratory: Boston, MA, USA, 2002. [Google Scholar]
  35. Üstün, T.B.; Chatterji, S.; Kostanjsek, N.; Rehm, J.; Kennedy, C.; Epping-Jordan, J.; Saxena, S.; Von Korff, M.; Pull, C. Developing the World Health Organization Disability Assessment Schedule 2.0. Bull. World Health Organ. 2010, 88, 815–823. [Google Scholar] [CrossRef]
  36. Hernandez, G.; Garin, O.; Pardo, Y.; Vilagut, G.; Pont, A.; Suárez, M.; Neira, M.; Rajmil, L.; Gorostiza, I.; Ramallo-Fariña, Y.; et al. Validity of the EQ–5D–5L and reference norms for the Spanish population. Qual. Life Res. 2018, 27, 2337–2348. [Google Scholar] [CrossRef] [Green Version]
  37. Hughes, M.E.; Waite, L.J.; Hawkley, L.C.; Cacioppo, J.T. A Short Scale for Measuring Loneliness in Large Surveys. Res. Aging 2004, 26, 655–672. [Google Scholar] [CrossRef]
  38. Rios, M.M.C.D.L.; Ortolá, R.; Rodríguez-Artalejo, F.; García-Esquinas, E. Exposure to secondhand tobacco smoke is associated with reduced muscle strength in US adults. Aging 2019, 11, 12674–12684. [Google Scholar] [CrossRef]
  39. Martínez-González, M.A.; López-Fontana, C.; Varo, J.J.; Villegas, A.S.; Martinez, J.A. Validation of the Spanish version of the physical activity questionnaire used in the Nurses’ Health Study and the Health Professionals’ Follow-up Study. Public Health Nutr. 2005, 8, 920–927. [Google Scholar] [CrossRef]
  40. Leon-Gonzalez, R.; Rodriguez-Artalejo, F.; Ortola, R.; Lopez-Garcia, E.; Garcia-Esquinas, E. Social Network and Risk of Poor Sleep Outcomes in Older Adults: Results from a Spanish Prospective Cohort Study. Nat. Sci. Sleep 2021, 13, 399–409. [Google Scholar] [CrossRef] [PubMed]
  41. García-Esquinas, E.; Rodríguez-Sánchez, I.; Ortolá, R.; Lopez-Garcia, E.; Caballero, F.F.; Rodríguez-Mañas, L.; Banegas, J.R.; Rodríguez-Artalejo, F. Gender Differences in Pain Risk in Old Age: Magnitude and Contributors. Mayo Clin. Proc. 2019, 94, 1707–1717. [Google Scholar] [CrossRef]
  42. García-Esquinas, E.; Andrade, E.; Martínez-Gómez, D.; Caballero, F.F.; López-García, E.; Rodríguez-Artalejo, F. Television viewing time as a risk factor for frailty and functional limitations in older adults: Results from 2 European prospective cohorts. Int. J. Behav. Nutr. Phys. Act. 2017, 14, 54. [Google Scholar] [CrossRef] [Green Version]
  43. Lobo, A.; Saz, P.; Marcos, G.; Día, J.L.; de la Cámara, C.; Ventura, T.; Morales, A.F.; Fernando, P.L.; Montanes, J.A.; Aznar, S. Evalidation and standardization of the cognition mini-exam (first Spanish version of the Mini-Mental Status Examination) in the general geriatric population. Med. Clin. 1999, 112, 767–774. [Google Scholar]
  44. Glatzer, W.; Gulyas, J. Cantril Self-Anchoring Striving Scale. In Encyclopedia of Quality of Life and Well-Being Research; Springer: Dordrecht, The Netherlands, 2014. [Google Scholar]
  45. Sun, Y.; Li, Y.; Bao, Y.; Meng, S.; Sun, Y.; Schumann, G.; Kosten, T.; Strang, J.; Lu, L.; Shi, J. Brief Report: Increased Addictive Internet and Substance Use Behavior During the COVID-19 Pandemic in China. Am. J. Addict. 2020, 29, 268–270. [Google Scholar] [CrossRef] [PubMed]
  46. Tabac, Alcool: Quel Impact du Confinement sur la Consommation Des Français? Available online: /presse/2020/tabac-alcool-quel-impact-du-confinement-sur-la-consommation-des-francais (accessed on 1 July 2021).
  47. Bommelé, J.; Hopman, P.; Walters, B.H.; Geboers, C.; Croes, E.; Fong, G.T.; Quah, A.C.K.; Willemsen, M. The double-edged relationship between COVID-19 stress and smoking: Implications for smoking cessation. Tob. Induc. Dis. 2020, 18, 63. [Google Scholar] [CrossRef]
  48. Chen, D. The psychosocial impact of the COVID-19 pandemic on changes in smoking behavior: Evidence from a nationwide survey in the UK. Tob. Prev. Cessat. 2020, 6, 1–5. [Google Scholar] [CrossRef]
  49. Xu, Y.; Li, Z.; Yu, W.; He, X.; Ma, Y.; Cai, F.; Liu, Z.; Zhao, R.; Wang, D.; Guo, Y.-F.; et al. The association between subjective impact and the willingness to adopt healthy dietary habits after experiencing the outbreak of the 2019 novel coronavirus disease (COVID-19): A cross-sectional study in China. Aging 2020, 12, 20968–20981. [Google Scholar] [CrossRef]
  50. Sánchez-López, M.D.P.; Dresch, V. The 12-Item General Health Questionnaire (GHQ-12): Reliability, external validity and factor structure in the Spanish population. Psicothema 2008, 20, 839–843. [Google Scholar]
  51. Yesavage, J.A.; Brink, T.; Rose, T.L.; Lum, O.; Huang, V.; Adey, M.; Leirer, V.O. Development and validation of a geriatric depression screening scale: A preliminary report. J. Psychiatr. Res. 1982, 17, 37–49. [Google Scholar] [CrossRef]
  52. Koopmann, A.; Georgiadou, E.; Kiefer, F.; Hillemacher, T. Did the General Population in Germany Drink More Alcohol during the COVID-19 Pandemic Lockdown? Alcohol Alcohol. 2020, 55, 698–699. [Google Scholar] [CrossRef]
  53. Tran, T.D.; Hammarberg, K.; Kirkman, M.; Nguyen, H.T.M.; Fisher, J. Alcohol use and mental health status during the first months of COVID-19 pandemic in Australia. J. Affect. Disord. 2020, 277, 810–813. [Google Scholar] [CrossRef]
  54. Neill, E.; Meyer, D.; Toh, W.L.; Van Rheenen, T.E.; Phillipou, A.; Tan, E.J.; Rossell, S.L. Alcohol use in Australia during the early days of the COVID-19 pandemic: Initial results from the COLLATE project. Psychiatry Clin. Neurosci. 2020, 74, 542–549. [Google Scholar] [CrossRef] [PubMed]
  55. Barbosa, C.; Cowell, A.J.; Dowd, W.N. Alcohol Consumption in Response to the COVID-19 Pandemic in the United States. J. Addict. Med. 2020. [Google Scholar] [CrossRef]
  56. Rossinot, H.; Fantin, R.; Venne, J. Behavioral Changes during COVID-19 Confinement in France: A Web-Based Study. Int. J. Environ. Res. Public Health 2020, 17, 8444. [Google Scholar] [CrossRef]
  57. Scarmozzino, F.; Visioli, F. Covid-19 and the Subsequent Lockdown Modified Dietary Habits of Almost Half the Population in an Italian Sample. Foods 2020, 9, 675. [Google Scholar] [CrossRef]
  58. Ismail, L.C.; Osaili, T.M.; Mohamad, M.N.; Al Marzouqi, A.; Jarrar, A.H.; Abu Jamous, D.O.; Magriplis, E.; Ali, H.I.; Al Sabbah, H.; Hasan, H.; et al. Eating Habits and Lifestyle during COVID-19 Lockdown in the United Arab Emirates: A Cross-Sectional Study. Nutrients 2020, 12, 3314. [Google Scholar] [CrossRef]
  59. Cancello, R.; Soranna, D.; Zambra, G.; Zambon, A.; Invitti, C. Determinants of the Lifestyle Changes during COVID-19 Pandemic in the Residents of Northern Italy. Int. J. Environ. Res. Public Health 2020, 17, 6287. [Google Scholar] [CrossRef]
  60. Deschasaux-Tanguy, M.; Druesne-Pecollo, N.; Esseddik, Y.; de Edelenyi, F.S.; Alles, B.; Andreeva, V.A.; Baudry, J.; Charreire, H.; Deschamps, V.; Egnell, M.; et al. Diet and physical activity during the COVID-19 lockdown period (March-May 2020): Results from the French NutriNet-Sante cohort study. MedRxiv 2021, 133, 924–938. [Google Scholar]
  61. Achón, M.; Serrano, M.; García-González, Á.; Alonso-Aperte, E.; Varela-Moreiras, G. Present Food Shopping Habits in the Spanish Adult Population: A Cross-Sectional Study. Nutrients 2017, 9, 508. [Google Scholar] [CrossRef] [PubMed]
  62. Bhutani, S.; Cooper, J.A. COVID-19–Related Home Confinement in Adults: Weight Gain Risks and Opportunities. Obesity 2020, 28, 1576–1577. [Google Scholar] [CrossRef] [PubMed]
  63. Fried, L.P.; Tangen, C.M.; Walston, J.; Newman, A.B.; Hirsch, C.; Gottdiener, J.; Seeman, T.; Tracy, R.; Kop, W.J.; Burke, G.; et al. Frailty in Older Adults: Evidence for a Phenotype. J. Gerontol. Ser. A Biol. Sci. Med. Sci. 2001, 56, M146–M157. [Google Scholar] [CrossRef]
  64. Meyer, J.; McDowell, C.; Lansing, J.; Brower, C.; Smith, L.; Tully, M.; Herring, M. Changes in Physical Activity and Sedentary Behavior in Response to COVID-19 and Their Associations with Mental Health in 3052 US Adults. Int. J. Environ. Res. Public Health 2020, 17, 6469. [Google Scholar] [CrossRef]
  65. Constant, A.; Conserve, D.F.; Gallopel-Morvan, K.; Raude, J. Socio-Cognitive Factors Associated With Lifestyle Changes in Response to the COVID-19 Epidemic in the General Population: Results from a Cross-Sectional Study in France. Front. Psychol. 2020, 11, 579460. [Google Scholar] [CrossRef]
  66. Martínez-De-Quel, Ó.; Suárez-Iglesias, D.; López-Flores, M.; Pérez, C.A. Physical activity, dietary habits and sleep quality before and during COVID-19 lockdown: A longitudinal study. Appetite 2021, 158, 105019. [Google Scholar] [CrossRef]
  67. Vahia, I.V.; Jeste, D.V.; Reynolds, C.F. Older Adults and the Mental Health Effects of COVID-19. JAMA 2020, 324, 2253. [Google Scholar] [CrossRef]
  68. Delussi, M.; Gentile, E.; Coppola, G.; Prudenzano, A.M.P.; Rainero, I.; Sances, G.; Abagnale, C.; Caponnetto, V.; De Cesaris, F.; Frattale, I.; et al. Investigating the Effects of COVID-19 Quarantine in Migraine: An Observational Cross-Sectional Study from the Italian National Headache Registry (RICe). Front. Neurol. 2020, 11, 597881. [Google Scholar] [CrossRef]
Figure 1. Baseline information collected in the study cohorts.
Figure 1. Baseline information collected in the study cohorts.
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Figure 2. Prospective association between baseline participant characteristics and changes in alcohol consumption or in adherence to the Mediterranean diet adherence screener (MEDAS) score during confinement.
Figure 2. Prospective association between baseline participant characteristics and changes in alcohol consumption or in adherence to the Mediterranean diet adherence screener (MEDAS) score during confinement.
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Figure 3. Prospective association between baseline participant characteristics and changes in physical activity and sedentary time during confinement.
Figure 3. Prospective association between baseline participant characteristics and changes in physical activity and sedentary time during confinement.
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Figure 4. Prospective association between baseline participant characteristics and changes in poor sleep quality score during confinement.
Figure 4. Prospective association between baseline participant characteristics and changes in poor sleep quality score during confinement.
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Table 1. Longitudinal changes in the prevalence of smoking, second-hand smoke, alcohol intake, diet quality, physical activity, weight, sedentary time, sleep characteristics, overall health, and pain between the COVID-19 pre-confinement (t0) and the confinement (t1) periods.
Table 1. Longitudinal changes in the prevalence of smoking, second-hand smoke, alcohol intake, diet quality, physical activity, weight, sedentary time, sleep characteristics, overall health, and pain between the COVID-19 pre-confinement (t0) and the confinement (t1) periods.
n/Total Participants for Each Variable and Study CohortMain Analyses
ENRICAESTSHAExernetModel 1Model 2
Tobacco exposure; RRR (95%CI) †
Former smokers521/1323139/464193/82971/4251.33 (1.05; 1.66)1.26 (1.00; 1.60)
Active smokers118/132373/46456/8297/4251.10 (0.88; 1.38)1.01 (0.80; 1.27)
Exposure to SHS; OR (95%CI) †70/1197 3.64 (1.70; 7.80)4.13 (1.95; 8.79)
Daily alcohol intake; RRR (95%CI) †
No371/1323135/46484/829 1.03 (0.77; 1.37)0.68 (0.54; 0.85)
Yes or almost daily 389/132378/464229/829 1.00 (0.77; 1.31)1.17 (0.97; 1.41)
Snack consumption; OR (95%CI) †603/1323 0.72 (0.60; 0.85)0.72 (0.60; 0.85)
Food to calm anxiety; OR (95%CI) †175/1323 0.54 (0.40; 0.73)0.56 (0.41; 0.76)
MEDAS index;x changes (95%CI) ‡1323464829425−0.53 (−0.61; −0.45)−0.53 (−0.60; −0.45)
Adherence to MEDAS items; OR (95%CI) †
Olive oil preference 13234648294253.17 (1.67; 6.01)4.27 (1.76; 10.36)
≥4 tbs of olive oil/day13234648294250.47 (0.39; 0.57)0.51 (0.42; 0.63)
2 srv vegetables/day13234648294250.38 (0.28; 0.48)0.50 (0.39; 0.65)
≥2 srv fruit/day13234648294250.70 (0.59; 0.85)0.78 (0.63; 0.96)
<2 srv red meat/day13234648294251.30 (1.07; 1.82)1.61 (1.21; 2.14)
<2 srv butter/day13234648294250.98 (0.73; 1.31)1.10 (0.81; 1.49)
<1 soda drink/day13234648294251.20 (0.89; 1.63)1.34 (0.97; 1.84)
≥7 glasses wine/week13234648294250.65 (0.51; 0.83)0.69 (0.53; 0.91)
≥2 srv legumes/week13234648294251.49 (1.23; 1.83)2.07 (1.63; 2.63)
≥2 srv fish/week13234648294250.72 (0.60; 0.86)0.86 (0.71; 0.99)
<2 srv sweets/week13234648294251.24 (1.05; 1.47)1.48 (1.23; 1.76)
≥2 srv nuts/week13234648294250.97 (0.81; 1.16)1.19 (0.96; 1.47)
poultry > red meat13234648294254.07 (3.26; 5.08)5.25 (4.05; 6.80)
≥2 srv sofrito/week13234648294250.35 (0.29; 0.42)0.33 (0.27; 0.40)
Weight;x changes (95%CI) ‡792241313221−0.09 (−0.32; 0.14)−0.57 (−1.29; 0.15)
Physical activity;x changes (95%CI) ‡
Overall (METs h/wk)1323 425−16.35 (−18.08; −14.6)−17.48 (−18.61; −16.35)
Recreational (METs h/wk)1323 425−10.95 (−12.02; −9.87)−11.32 (−12.24; −10.41)
Household (METs h/wk) 1323 425−5.39 (−6.66; −4.12)−6.04 (−7.11; −4.98)
PASE score 832 −6.42 (−11.14; −1.70)−16.66 (−19.59; −13.73)
Sedentary time;x changes (95%CI) ‡
Overall (min/day)1323 42591.89 (81.61; 102.1)91.68 (81.21; 102.11)
TV time (min/day)1323 27.18 (19.56; 34.80)27.93 (20.23; 35.63)
Other screen time (min/day)1319 50.20 (45.57; 54.83)50.60 (45.83; 55.44)
Reading (min/day)1323 16.30 (12.34; 20.25)15.53 (11.37; 19.58)
Listening to music (min/day)1323 7.52 (4.61; 10.43)7.25 (4.26; 10.24)
Sleep characteristics;x changes (95%CI) ‡
Hours/night-time sleep1323464829425−0.02 (−0.08; 0.04)−0.00 (−0.06; 0.05)
Minutes/day-time sleep1317 421−12.50 (−14.18; −10.8)−12.08 (−13.73; −10.43)
Poor sleep quality score1289430 3950.13 (0.10; 0.16)0.12 (0.09; 0.15)
Nº poor sleep indicators1285 0.06 (−0.02; 0.14)0.08 (0.00; 0.15)
Overall health §; x changes (95%CI)
SF-12, PCS ‡1311 5.03 (4.45; 5.60)4.79 (4.72; 5.38)
SF-12, MCS ‡1311 −1.20 (−1.80; −0.58)−1.19 (−1.81; −0.58)
WHODAS-12 464 2.57 (1.29; 3.84)−0.18 (−1.85; 1.48)
Pain scale;x changes (95%CI) ‡1296 0.17 (0.06; 0.30)0.18 (0.05; 0.30)
ENRICA: Seniors-ENRICA-2. ES: Edad con Salud. TSH: Toledo Study for Healthy Aging. x: mean change. OR: odds ratio; 95%CI: 95% confidence interval; MEDAS: Mediterranean Diet Assessment Score; Met: Metabolic Equivalent to Task; MCS: Mental Component Score of the SF-12; PA: Physical Activity; PCS: Physical Component Score of the SF-12; rPA; SHS: second-hand smoke. † Odds ratios and relative risk ratios (RRR) (95% confidence intervals) for tobacco smoke exposure, alcohol intake, snack consumption, intake of food consumption to calm anxiety, short- or long-sleep duration, and poor sleep quality between the pre-confinement and confinement periods were obtained from multilevel mixed effects logistic (OR) or multilevel structural equation models (RRR), with robust standard errors accounting for within-participant correlations induced by repeated measures. ‡ Average differences (95% confidence intervals) in MEDAS, weight, physical activity, sedentary time, hours of night- or day-time sleep, and number of poor sleep quality indicators between the pre-confinement and confinement periods were obtained from repeated measures linear regression models with robust standard errors accounting for within-participant correlations induced by repeated measures. § Higher scores in the mental component and physical component of the SF-12 and lower scores in the WHODAS-12 are indicative of better health. Model 1 adjusted for age, sex (men or women), educational level (primary or less, secondary, or university), civil status (married, widowed, single, or divorced), and study cohort. Model 2 further adjusted for baseline body mass index (normoweight, overweight, or obese), and chronic comorbidities (hypertension, diabetes, osteo-muscular disease, and depression), as well as for changes over time in cohabitation (living alone, not living alone), smoking (never, former or current), adherence to the Mediterranean diet (MEDAS score), physical activity (cohort-specific quartiles), hours of night-time sleep (normal, short sleep or long sleep), and overall health (in quartiles).
Table 2. Prospective association between participant characteristics and changes in the mental component (MCS) and physical component (PCS) scores of the SF-12 (n = 1243 from Seniors-ENRICA-2), the WHODAS-12 (n = 460 from Edad con Salud), and the pain score (n = 983 from Seniors-ENRICA-2) during the COVID-19 confinement. Increases in MCS or PCS components reflect improvements in health, while increases in the WHODAS-12 or pain scores reflect worsening in health or pain, respectively.
Table 2. Prospective association between participant characteristics and changes in the mental component (MCS) and physical component (PCS) scores of the SF-12 (n = 1243 from Seniors-ENRICA-2), the WHODAS-12 (n = 460 from Edad con Salud), and the pain score (n = 983 from Seniors-ENRICA-2) during the COVID-19 confinement. Increases in MCS or PCS components reflect improvements in health, while increases in the WHODAS-12 or pain scores reflect worsening in health or pain, respectively.
Changes in Physical Component ScoreChanges in Mental Component ScoreChanges in WHODAS-12Changes in Pain Scale †
x (95%CI); n = 1243x (95%CI); n = 1243x (95%CI); n = 1460x (95%CI); n = 983
Sociodemographic factors
Age, yr−0.19 (−0.29; −0.08)0.12 (0.00; 0.23)0.14 (−0.05; 0.33)0.01 (−0.01; 0.04)
Female−0.16 (−1.21; 0.89)−2.46 (−3.65; −1.35)−0.93 (−3.73; 1.88)0.28 (0.03; 0.51)
Education
Primary or lessRef.Ref.Ref.Ref.
Secondary−0.17 (−1.28; 0.93)0.18 (−1.02; 1.38)−0.63 (−3.57; 2.32)−0.05 (−0.31; 0.21)
University0.90 (−0.20; 1.99)0.11 (−1.08; 1.31)−4.12 (−7.70; −0.53)−0.13 (−0.30; 0.12)
Civil status
MarriedRef.Ref.Ref.Ref.
Single−0.74 (−2.74; 1.25)2.16 (0.00; 4.33)2.68 (−3.82; 9.28)0.29 (−0.19; 0.76)
Divorced−0.02 (−2.05; 2.01)0.94 (−1.26; 3.15)1.80 (−2.78; 6.39)0.20 (−0.31; 0.70)
Widowed−0.75 (−2.20; 0.69)1.24 (−0.33; 2.81)−1.79 (−6.04; 2.45)0.14 (−0.21; 0.49)
Living alone0.74 (−0.72; 2.20)−1.40 (−3.00; 0.09)−0.10 (−4.06; 3.87)−0.12 (−0.48; 0.23)
No daily contact with family/friends other than cohabitants0.23 (−1.04; 1.50)−0.24 (−1.62; 1.14)0.46 (−2.24; 3.17)0.06 (−0.05; 0.18)
Feeling lonely0.22 (−0.26; 0.70)−1.02 (−1.54; −0.50)0.37 (−0.78; 1.52)0.06 (−0.05; 0.18)
Housing conditions
Lack of outdoor views0.40 (−1.12; 1.92)−0.94 (−2.60; 0.71)3.29 (−0.93; 7.51)0.14 (−0.22; 0.50)
Lack of terrace/balcony0.27 (−0.69; 1.21)0.23 (−0.80; 1.27)−1.95 (−4.56; 0.66)−0.05 (−0.28; 0.18)
Lack of garden/yard−1.38 (−2.60; −0.16)−0.44 (1.78; 0.89)−1.09 (3.77; 1.60)0.02 (−0.28; 0.18)
No internet access0.45 (−0.66; 1.56)−0.50 (−1.70; 0.70)1.61 (−1.62; 4.84)−0.02 (−0.28; 0.24)
Too much noise1.62 (−1.18; 4.42)−5.05 (−8.10; −2.00)−0.00 (−5.80; 5.79)0.74 (0.10; 1.38)
Lifestyle behaviors
Smoking
Never smokers Ref.Ref.Ref.Ref.
Former smokers 0.12 (−0.83; 1.08)0.22 (−0.81; 1.26)−1.93 (−4.88; 1.03)0.05 (−0.17; 0.27)
Smoker0.10 (−1.42; 1.61)−0.62 (−2.27; 1.03)0.95 (−2.73; 4.62)−0.13 (−0.48; 0.22)
Alcohol intake
Not drinkerRef.Ref.Ref.Ref.
Drinker, not daily −0.05 (−1.08; 0.99)−0.23 (−1.36; 0.90)−0.02 (−2.92; 2.88)0.03 (−0.21; 0.28)
Drinker, daily/almost daily−0.15 (−2.22; 0.92)−0.33 (−1.49; 0.84)−0.94 (−4.60; 2.72)0.08 (−0.17; 0.33)
MEDAS−0.02 (−0.27; 0.23)0.11 (−0.16; 0.38)−0.28 (−0.98; 0.42)0.06 (−0.00; 0.12)
PA (cohort-specific quartiles)
1st quartile (less)Ref.Ref.Ref.Ref.
2nd quartile0.58 (−0.59; 1.75)−0.74 (−2.01; 0.53)−2.64 (−6.07; 0.79)0.06 (−0.22; 0.33)
3rd quartile1.61 (0.40; 2.83)−1.05 (−2.34; 0.28)−5.48 (−8.92; −2.02)−0.12 (−0.40; 0.16)
4th quartile 1.03 (−0.25; 2.31)−1.35 (−2.75; 0.05) *−4.20 (−7.90; −0.49) *−0.02 (−0.32; 0.28)
BMI
NormoweightRef.Ref.Ref.Ref.
Overweight−0.11 (−1.10; 0.89)0.05 (−1.03; 1.13)−1.23 (−4.20; 1.75)−0.14 (−0.37; 0.09)
Obese−0.14 (−1.38; 1.10)−0.29 (−1.64; 1.06)−1.18 (−4.47; 2.10)−0.05 (−0.34; 0.24)
ST (cohort-specific quartiles)
1st quartile (less time)Ref.Ref.Ref.Ref.
2nd quartile−0.31 (−1.48; 0.86)−0.55 (−1.83; 0.71)0.32 (−3.05; 3.68)0.24 (−0.04; 0.51)
3rd quartile−0.26 (−0.89; 1.41)−1.06 (−2.31; 0.19)−0.39 (−3.62, 2.85)−0.06 (−0.33; 0.21)
4th quartile −0.53 (−1.71; 0.64)−0.16 (−1.43; 1.12)3.39 (−0.38; 7.15)−0.03 (−0.31; 0.25)
Sleep characteristics
Hours of night-time sleep
Normal sleepRef.Ref.Ref.Ref.
Short sleep (≤6 h)−0.62 (−1.76; 0.51)−0.04 (−1.27; 1.19)1.03 (−2.65; 4.70)0.46 (0.19; 0.73)
Long sleep (≥9 h)0.67 (−1.34; 2.68)−1.32 (−3.51; 0.87)−1.76 (−5.62; 2.11)−0.29 (−0.76; 0.17)
Hours of day-time sleep ‡
NoneRef.Ref.Ref.
Short nap (≤30 min)0.04 (−0.93; 1.01)−1.15 (−2.20; −0.10) −0.11 (−0.34; 0.11)
Long nap (30–60 min)−0.81 (−2.08; 0.46)0.50 (−0.87; 1.87) −0.04 (−0.34; 0.25)
Very long nap (≥60min)1.26 (−1.74; 2.27)−2.49 (−4.66; −0.33) −0.19 (−0.66; 0.27)
Overall sleep quality
Very good−0.47 (−1.81; 0.87)2.09 (0.64; 3.53)−0.58 (−3.20; 2.05)0.04 (−0.27; 0.35)
GoodRef.Ref.Ref.Ref.
Fair−0.65 (−1.73; 0.44)−1.92 (−3.01; −0.75)3.15 (−1.38; 7.68)0.18 (−0.08; 0.43)
Poor/very poor−4.04 (−7.07; −1.02) *0.49 (−2.78; 3.77)−3.79 (−16.7; 9.10)−0.04 (−0.83; 0.75)
Health-related variables
Overall health
1st quartile Ref.
2nd quartile −0.46 (−0.80; −0.13)
3rd quartile −0.56 (−0.92; −0.22)
4th quartile (best) −0.64 (−1.00; −0.27) †
Chronic morbidities
Diabetes0.56 (−0.54; 1.67)−0.22 (−1.42; 0.30)0.32 (−3.02; 3.67)−0.05 (−0.32; 0.22)
Hypertension−0.22 (−1.08; 0.64)−0.55 (−1.49; 0.39)−0.30 (−2.83; 2.23)0.05 (−0.15; 0.25)
CVD−2.53 (−4.72; −0.34)0.98 (−1.41; 3.36)−0.59 (−4.52; 3.33)0.24 (−0.22; 0.49)
Cancer−1.98 (−3.76; −0.20)−0.81 (−2.75; 1.13)0.84 (−3.21; 4.89)0.19 (−0.27; 0.66)
Osteo-muscular disease−0.69 (−1.58; 0.21)0.33 (−0.65; 1.30)2.49 (−0.13; 5.10)0.57 (0.36; 0.79)
Depression−1.87 (−3.39; −0.34)−1.36 (−3.91; 0.30)0.88 (−4.50; 13.05)0.30 (0.00; 0.65)
Mobility limitations−2.37 (−3.49; 1.25)−1.67 (−2.90; −0.44) 0.25 (0.01; 0.50)
Negative aging experience scale−0.16 (−0.58; 0.26)−0.85 (−1.31; −0.40) 0.02 (−0.08; 0.12)
Cantril Ladder0.28 (0.03; 0.52)0.20 (−0.06; 0.47) −0.11 (−0.16; −0.05)
Low MMSE score (<23)1.59 (−1.16; 4.34)−3.24 (−6.23; −0.26) 0.18 (−0.52; 0.88)
Years since baseline examination−0.50 (−1.46; 0.47)0.48 (−0.57; 1.54)0.50 (−1.46; 0.47)−0.23 (−0.46; −0.00)
Week of the State of Alarm−0.64 (−1.07; −0.20)0.99 (0.52; 1.46)0.39 (−0.67; 1.45)0.10 (0.00; 0.20)
x: mean change. 95%CI: 95% confidence interval; MEDAS: Mediterranean Diet Assessment Score; PA: physical activity; BMI: body mass index; ST: sedentary time; PCS: Physical Component Score of the SF-12; MCS: Mental Component Score of the SF-12; MMSE: Mini-Mental State Examination. † The pain scale ranged 0 (no pain) to 7 (worst pain) and was created based on pain frequency, pain intensity (assessed according to its impact on habitual activities), and number of pain sites. Sporadic (<2 times/week) and frequent (≥2 times/week) pain were assigned a score of 1 and 2, respectively; light, moderate, and high intensity, a score of 1, 2, and 3, respectively; and 1–2 and ≥3 sites a score of 1 and 2, respectively. ‡ Information only available in the Seniors ENRICA-2 cohort. * p-value for trend <0.05. All models were adjusted for baseline age, sex (men or women), educational level (primary or less, secondary, or university), civil status (married, widowed, single, divorced), housing conditions (lack of outdoor views, terrace/balcony, private garden/yard, lack of internet, and noise), smoking status (never, former, or current), adherence to the Mediterranean diet (MEDAS score), body mass index (normoweight, overweight, or obese), physical activity (cohort-specific quartiles), hours of night-time sleep (normal, short sleep, long sleep), chronic comorbidities (hypertension, diabetes, osteo-muscular disease, and depression), time since last follow-up visit, cohort of study, and week of the State of Alarm. Models for MCS and PCS components of the SF-12 adjusted for baseline values of the PCS and the MCS, respectively.
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García-Esquinas, E.; Ortolá, R.; Gine-Vázquez, I.; Carnicero, J.A.; Mañas, A.; Lara, E.; Alvarez-Bustos, A.; Vicente-Rodriguez, G.; Sotos-Prieto, M.; Olaya, B.; et al. Changes in Health Behaviors, Mental and Physical Health among Older Adults under Severe Lockdown Restrictions during the COVID-19 Pandemic in Spain. Int. J. Environ. Res. Public Health 2021, 18, 7067. https://doi.org/10.3390/ijerph18137067

AMA Style

García-Esquinas E, Ortolá R, Gine-Vázquez I, Carnicero JA, Mañas A, Lara E, Alvarez-Bustos A, Vicente-Rodriguez G, Sotos-Prieto M, Olaya B, et al. Changes in Health Behaviors, Mental and Physical Health among Older Adults under Severe Lockdown Restrictions during the COVID-19 Pandemic in Spain. International Journal of Environmental Research and Public Health. 2021; 18(13):7067. https://doi.org/10.3390/ijerph18137067

Chicago/Turabian Style

García-Esquinas, Esther, Rosario Ortolá, Iago Gine-Vázquez, José A. Carnicero, Asier Mañas, Elvira Lara, Alejandro Alvarez-Bustos, German Vicente-Rodriguez, Mercedes Sotos-Prieto, Beatriz Olaya, and et al. 2021. "Changes in Health Behaviors, Mental and Physical Health among Older Adults under Severe Lockdown Restrictions during the COVID-19 Pandemic in Spain" International Journal of Environmental Research and Public Health 18, no. 13: 7067. https://doi.org/10.3390/ijerph18137067

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