Urinary incontinence (UI) is a distressing condition that limits women’s quality of life and places a heavy burden on health care services. Behavioural treatments are recommended as a first-line treatment. An evidence-based self-management package was developed following the Medical Research Council (MRC) framework for complex interventions. This study aimed to evaluate the feasibility and acceptability of the intervention.
Methods
A mixed-methods approach was undertaken, namely a randomised controlled feasibility study with nested qualitative study. Fifty women aged 55 or over living with UI, recruited from community centres were randomly assigned to either a 3-month course with the package with a support session or a control group to receive the same package only 3 months later. Principal outcome measures were: self-reported quality of life, UI severity, self-efficacy and psychological status. Analysis of covariance was undertaken to estimate within- and between- group changes for all outcomes. Acceptability was explored using individual interviews at follow-up.
Results
Fifty women were randomised (24 to intervention, 26 to control); mean age of 69.7 (±9.1) years and mean UI frequency 2.2 (±2.2) episodes/day at baseline. Overall, 49 women (98%) completed 3-month follow-up (24 in the intervention, 25 in the control). A positive trend was detected in the impact of UI on their personal relationships (− 3.89, p = 0.088), symptom severity (− 1.77, p = 0.025), UI symptoms scale (− 1.87, p = 0.031) and anxiety status (− 2.31, p = 0.001), respectively. Changes in quality of life and self-efficacy did not differ significantly between groups. Majority of women (71%) in the intervention group reported subjective improvement after 3 months. Spearman correlation coefficient was 0.43 (p < 0.05) between their subjective perception of change and self-efficacy. Women perceived the package being acceptable and described that the package had the potential to increase their knowledge and confidence to manage symptoms and improve quality of life.
Conclusions
The study demonstrated that the self-management package is feasible and acceptable for older women with UI. Further studies are needed with a large sample size in clinical settings to evaluate the effectiveness of this package.
Trial registration
ISRCTN17194896. Registered on 11th September 2019 (retrospectively registered).
Hinweise
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Abkürzungen
MRC
Medical Research Council
PFME
Pelvic floor muscle exercises
RCT
Randomised controlled trial
UI
Urinary incontinence
Background
Urinary incontinence (UI) is a distressing condition that limits people’s quality of life and places a burden on those affected and health and social care services [1, 2]. Prevalence in women is estimated to be around about 40%, with an increase with age [3]. Women living with UI often experience functional limitations and social embarrassment, negatively impacting their mental health [4]. Although several options are available for treating and managing UI, behavioural treatments are recommended as a first-line treatment therapies for stress, urgency and mixed UI by international UI guidelines developed worldwide [5], prior to considering more intensive treatments.
Behavioural treatment programmes focusing on single elements of behavioural strategies have been extensively researched, e.g. pelvic floor muscle exercises (PFME) [6]. These programmes are sometimes challenging to deliver as they need multiple appointments, the involvement of specialised practitioners, and may lack flexibility to respond to individual needs associated with comorbidities in older women. Many women therefore choose to disengage with the service. Only a third of women with UI consult a doctor in European countries such as France, Germany, Spain and the UK, and 20 to 25% of those experiencing significant clinical symptoms seek care and less than half of them receive treatment [7]. A multifaceted intervention involving behavioural strategies may be more effective than a single component for the management of UI in older women [8, 9].
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Self-management for chronic conditions is multidimensional and defined as an intervention designed to develop individuals’ knowledge, skills or psychological and social resources and their ability to manage their health condition and consequences, through education, training and support [10]. Many self-management interventions have been developed to support people to cope with their health conditions and improve quality of life. Positive outcomes reported include a higher degree of self-efficacy, reduced physical interference, and improved mental health status at follow-up [11‐21]. Although evidence for self-management programmes incorporating multifaceted behavioural treatments for use in UI among older women is currently limited, our systematic review concluded that multifaceted self-management interventions including PFME, bladder retraining, or combination behavioural techniques are beneficial.
Following the Medical Research Council (MRC) framework for developing and evaluating complex interventions [22], a self-management package was co-developed with older women with UI and health professionals providing treatment and care. The initial draft of the intervention was informed by synthesis of data from a systematic review and stakeholder interviews with women and health professionals. Both groups preferred an evidence-based self-management package that had the capacity to meet women’s individual needs with the flexibility to modify behaviours in coping with UI without significant service provision and/or intensive interaction with health professionals. The initial draft was reviewed and discussed in detail with an expert group which consisted of four women with UI, five health professionals and two lay members. Consensus was reached on the content and format of this self-management package for older women with UI using a normal group technique [23]. However, the feasibility and acceptability of the intervention remained unknown.
Methods
Aim
The aim of this study was to evaluate the feasibility, acceptability, and preliminary outcomes of an evidence-based self-management package for UI in older women. Specifically, it was to 1) assess the feasibility of the intervention to evaluate the effectiveness of a self-management package; 2) assess the variation of the main outcome measures to inform sample size considerations for a full randomised controlled trial (RCT); 3) provide preliminary data on the effect of the intervention; 4) understand the benefits/limitations and acceptability of the self-management package compared to no active treatment.
Design
A mixed-methods approach comprising a two-arm RCT feasibility study with a nested qualitative study was undertaken. The qualitative study was conducted to understand how the intervention might work and explore facilitators and barriers to acceptance of the intervention [24]. This study presented adheres to CONSORT guidelines.
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Patient and public engagement
A project advisory group comprising three older women (aged 55 plus) living with UI and one nurse working in a community continence clinic was set up prior to the commencement of this study, to ensure this study addressed issues that were important and relevant to women. The meeting was led by YF and facilitated by LMc/EAN every 6 months. Participants were provided with background information and clinical guidelines for UI management and consulted for their current experiences and expectations of managing UI. They also reviewed the findings of the systematic review and interview transcripts. All highlighted the need for evidence-based practice that has the ability to engage the wider population and indicated a willingness to use it for UI self-management. The group also supported the application of ethics approval and development of interview schedules.
Setting
This is a single-centre, randomised controlled feasibility study of self-management package versus wait-list control with 12- week post-intervention follow up. Participants were recruited using flyers posted in community centres of a local Forum for older people in West Yorkshire, UK. A short presentation was also given by the project researcher in most centres.
Participants
Women were eligible if they were aged 55 or over, had self-reported symptom of involuntary leakage of urine and were able to read and speak English. Individuals who self-reported their UI were caused by neurological diseases affecting the brain and spinal cord, or were cognitively impaired were excluded.
A consecutive sampling strategy was applied to recruit participants in this study. Assuming an attrition rate of 20%, a target of 25 per arm was sufficient to have 20 participants in each arm by the end of the study. This has been recommended as acceptable for a feasibility trial assuming at worst a medium effect size (Cohen’s d = 0.2) for a continuous outcome and 80% power [25].
Randomisation
All participants were recruited prior to randomisation to the intervention. Eligible women were randomised using a 1:1 ratio to either the intervention or control group. The randomisation procedure was performed by a web-based randomisation service (https://sealedenvelope.com/). Due to the nature of the intervention, this study is considered open-label and is not allocation concealed because the researcher delivering the interventions and the participants were aware of group allocation at the time of implementation.
Intervention
The experimental intervention was the self-management package, co-developed with older women living with UI, health professionals and lay members. The aim of the package was to provide information and practical skills for women to self-manage their UI and other symptoms. Following elements were included: recognition and awareness, getting the support you need, understanding the cause, learning to manage your UI, developing a self-management plan and how can you find out more. Descriptions of self-management techniques such as PFME, bladder training and lifestyle interventions were also provided. The researcher acted as a facilitator and delivered the intervention in person immediately after the completion of baseline data collection. A self-management brochure was also distributed. The intervention group could request a single one-hour support session with the researcher if they had any difficulties in using the package.
The control group did not receive the self-management package or the support session. However they had been given a copy of the same package upon the completion of their follow-up data collection (at 3 months).
Outcome measures
As this was a feasibility study it was appropriate to explore a range of outcome measures. Standardised self-reported measures were used to assess participants’ generic and disease-specific quality of life, UI severity, self-efficacy and psychological health respectively: the EuroQol (EQ-5D-5 L) [26], King’s Health Questionnaire (KHQ) [27], International Consultation on Incontinence Questionnaire – urinary incontinence short form (ICIQ-UI SF) [28, 29], Geriatric Self-Efficacy index for urinary incontinence (GSE-UI) [30], and Hospital Anxiety and Depression Scale (HADS) [31]. Data were collected at baseline and three-month follow-up. Patient Global Impression: Improvement (PGI-I) was obtained from the intervention group only at three-month follow up [32]. These measures have been commonly used in research and practice for women with UI.
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Data analysis
Descriptive analyses were undertaken to establish recruitment, drop-out rates and the distribution of baseline and follow-up characteristics and outcomes. For each of the above measures, analysis of covariance (ANCOVA) was conducted adjusting for their baseline values to take account of outcome imbalance at baseline and estimate the impact of intervention compared with control [33, 34]. T-tests and Chi-square tests were applied to compare two groups at baseline and follow-up for continuous and categorical variables, respectively. Intention-to-treat analysis was performed for this study. Data from all subjects were included in the analysis as randomised. To test the appropriateness of the analysis, complete case analysis was undertaken for each of the above outcome measures to identify the relative treatment effects using a linear (for continuous variables) and logistic (for binary outcomes) mixed model. For all analyses, a two-tailed p-value less than 0.05 was considered statistically significant and a p-value between 0.05 and 0.1 was interpreted as indicating a trend [35, 36].
Nested qualitative study
Women in the intervention group were eligible to participate in this subsequent qualitative study aiming to understand the acceptability of the package. They were purposively recruited considering different types of UI, number of years living with UI, to enable wider discussions on the self-management package and their experience. The concept of data saturation guided sample size for this qualitative study [37].
Semi-structured individual interviews using open-ended questions were undertaken at follow-up. Interviews were conducted either face-to-face in the participants’ homes, in a meeting room at the University, or by telephone, based on participants’ preferences. Interviews were digitally recorded with permission and transcribed verbatim for analysis. Interviews focused on exploring participants’ experience of managing symptoms guided by the intervention, facilitators and barriers to the use of the package, comments on the content and format, feedback on outcome measures used and suggestions on dissemination strategy.
Data analysis was commenced during the interview phase and the transcription, and continued during the analysis of the transcriptions, hence early commencement of analysis facilitated the development of subsequent interviews [38]. Data were analysed using thematic analysis [39], involving a six-step procedure: familiarising the data, generating initial codes, searching for themes, reviewing themes, defining and naming themes, and producing the report. Although they were presented as a step-by-step procedure, the analysis was an iterative and reflexive process to finalise the themes. To ensure trustworthiness and rigour of the analysis, we double coded the data as a validity check and explored alternative interpretations of the data and through discussion with members of the research team. Interview transcripts were managed and analysed using Nvivo, a qualitative software programme for organising and coding the data [40].
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Results
Participants characteristics
Overall 50 participants (Mage =69.7, SD = 9.1), were randomly allocated to either intervention (n = 24, Mage =69.5, SD = 8.9) or control group (n = 26, Mage =69.8, SD = 9.5). During the 3 months follow-up, no one in the intervention group requested the support session with the researcher. One woman in the control group dropped out due to admission to the hospital for other health conditions. A total of 49 participants with a mean age 69.6 (SD = 9.1) were included in the complete case analysis. No significant differences were found for all demographics and UI characteristics collected at baseline, indicating that randomisation was achieved between the intervention and control groups. The majority were white British (77.6%), completed secondary and higher education (91.8%), were retired (71.4%), and had delivered 2 or more children (71.5%). The number of participants was similar across different UI types. Please see participant’s characteristics in Table 1.
Table 1
Baseline demographics and characteristics
Variable
Overall
Intervention group
Control group
p-value
n
%
n
%
n
%
Total
49
24
25
Age (Mean, SD)
69.7
9.1
69.5
8.9
69.6
9.6
0.994
Ethnicity
0.157
White British
38
77.6%
16
66.7%
22
88.0%
Asian Indian
9
18.4%
7
29.2%
2
8.0%
Mixed White and Black African
2
4.1%
1
4.2%
1
4.0%
Education
0.486
Primary
4
8.2%
3
12.5%
1
4.0%
Secondary
16
32.7%
9
37.5%
7
28.0%
Further
14
28.6%
5
20.8%
9
36.0%
Higher
15
30.6%
7
29.2%
8
32.0%
Religion
0.108
No religion
9
18.4%
5
20.8%
4
16.0%
Christian
31
63.3%
12
50.0%
19
76.0%
Hindu
9
18.4%
7
29.2%
2
8.0%
Marital status
0.365
Single
6
12.2%
3
12.5%
3
12.0%
Married
27
55.1%
15
62.5%
12
48.0%
Separated
1
2.0%
0
0.0%
1
4.0%
Divorced
3
6.1%
0
0.0%
3
12.0%
Widowed
12
24.5%
6
25.0%
6
24.0%
Employment
0.573
Full time employed
3
6.1%
1
4.2%
2
8.0%
Part time employed
5
10.2%
3
12.5%
2
8.0%
Self employed
1
2.0%
0
0.0%
1
4.0%
Not in paid employment
2
4.1%
1
4.2%
1
4.0%
Unemployed-looking for work
1
2.0%
0
0.0%
1
4.0%
Retired
35
71.4%
19
79.2%
16
64.0%
Unable to work
2
4.1%
0
0.0%
2
8.0%
Children
0.421
None
11
22.4%
5
20.8%
6
24.0%
1
3
6.1%
1
4.2%
2
8.0%
2
18
36.7%
9
37.5%
9
36.0%
3
11
22.4%
4
16.7%
7
28.0%
UI type
0.672
Stress UI
14
28.6%
8
33.3%
6
24.0%
Urge UI
17
34.7%
7
29.2%
10
40.0%
Mixed UI
18
36.7%
9
37.5%
9
36.0%
Frequency of UI (average per day)
0.070
None
16
32.7%
12
50.0%
4
16.0%
1
8
16.3%
3
12.5%
5
20.0%
2
5
10.2%
1
4.2%
4
16.0%
3
9
18.4%
5
20.8%
4
16.0%
4+
11
22.4%
3
12.5%
8
32.0%
UI urinary incontinence
Outcome measures
Medians, interquartile range (IQR), mean, standard deviation (SD) and p-values of all baseline and follow-up outcomes are shown in Tables 2 and 3, respectively. There were no differences shown in general quality of life, UI symptoms scale and emotional health status at baseline, however groups differed with regard to KHQ severity measures (34.03 vs 48.67, p = 0.028) and self-efficacy (84.96 vs 57.76, p < 0.001). At follow-up, differences were detected in KHQ symptom severity (6.38 vs 9.04, p = 0.006), UI symptoms scale (5.38 vs 7.76, p = 0.022), self-efficacy (89.13 vs 69.08, p = 0.007), and anxiety (5.13 vs 7.80, p = 0.049) at 3-month follow-up.
Table 2
Median, interquartile range (IQR), mean, standard deviation (SD) and p-values of outcome measurements at baseline
Variable
Dimensions
Intervention group
Control group
p-value
n
%
Median
IQR
Mean
SD
n
%
Median
IQR
Mean
SD
EQ-5D-5L
Mobility
0.675
No/slight problem
18
75.0%
20
80.0%
Moderate/Severe/extreme problem
6
25.0%
5
20.0%
Selfcare
0.527
No/slight problem
22
91.7%
24
96.0%
Moderate/Severe/extreme problem
2
8.3%
1
4.0%
Usual activities
0.662
No/slight problem
19
79.2%
21
84.0%
Moderate/Severe/extreme problem
5
20.8%
4
16.0%
Pain & discomfort
0.315
No/slight problem
14
58.3%
18
72.0%
Moderate/Severe/extreme problem
10
41.7%
7
28.0%
Anxiety & depression
0.524
No/slight problem
20
83.3%
19
76.0%
Moderate/Severe/extreme problem
4
16.7%
6
24.0%
Index
24
0.90
0.23
0.82
0.17
25
0.83
0.14
0.79
0.19
0.643
VAS
24
77.50
27.50
71.67
18.04
25
70.00
25.00
64.40
25.59
0.258
KHQ
Part I
General health perception (0-100)
24
25.00
25.00
33.33
21.70
25
25.00
25.00
32.00
15.34
0.804
Incontinence impact (0-100)
24
33.33
33.33
45.83
23.70
24
66.67
33.33
56.94
20.80
0.091
Part II
Role limitations (0-100)
24
16.67
33.33
20.14
22.51
25
33.33
33.33
33.33
24.06
0.054
Physical limitations (0-100)
24
16.67
41.67
22.92
22.42
25
33.33
33.33
30.67
20.79
0.216
Social limitations (0-100)
24
0.00
13.89
9.03
13.19
25
0.00
22.22
16.44
24.40
0.195
Personal relationships (0-100)
15
0.00
0.00
5.56
12.06
14
0.00
0.00
11.90
25.68
0.396
Emotions (0-100)
24
11.11
22.22
16.67
19.93
24
11.11
11.11
17.59
14.98
0.856
Sleep/energy (0-100)
24
33.33
41.67
37.50
28.34
25
50.00
50.00
47.33
32.16
0.263
Severity measures (0-100)
24
33.33
29.17
34.03
22.10
25
41.67
33.33
48.67
22.91
0.028
Part III
Symptom severity scale (0-30)
24
7.50
5.50
8.00
4.39
25
10.00
3.00
9.92
4.06
0.119
ICIQ-UI SF
Scale (0-21)
24
8.00
6.50
8.63
4.03
25
9.00
6.00
9.68
4.19
0.374
GSE-UI
Scale (0-120)
24
84.50
33.50
84.96
18.89
25
55.00
23.00
57.76
23.55
0.000
HADS
Anxiety scale (0-21)
24
6.50
6.50
7.13
5.12
25
7.00
5.00
7.56
4.56
0.755
Normal
13
54.2%
13
52.0%
0.868
Mild
7
29.2%
6
24.0%
Moderate
2
8.3%
4
16.0%
Severe
2
8.3%
2
8.0%
Depression scale (0-21)
24
3.00
3.50
3.67
3.29
25
3.00
4.00
3.88
4.02
0.840
Normal
20
83.3%
23
92.0%
0.318
Mild
2
8.3%
0
0.0%
Moderate
2
8.3%
1
4.0%
Severe
0
0
T-tests for continuous variables and chi-square tests for categorical variablesVAS Visual Analogue Scale, KHQ King’s Health Questionnaire, ICIQ-UI SF International Consultation on Incontinence Questionnaire – urinary incontinence short form, GSE-UI Geriatric Self-Efficacy index for urinary incontinence, HADS Hospital Anxiety and Depression Scale
Table 3
Median, interquartile range (IQR), mean, standard deviation (SD) and p-values of outcome measurements at 12-week follow up
Variable
Dimensions
Intervention group
Control group
p-value
n
%
Median
IQR
Mean
SD
n
%
Median
IQR
Mean
SD
EQ-5D-5L
Mobility
0.478
No/slight problem
21
87.5%
20
80.0%
Moderate/Severe/extreme problem
3
12.5%
5
20.0%
Selfcare
0.322
No/slight problem
24
100.0%
24
96.0%
Moderate/Severe/extreme problem
0
0.0%
1
4.0%
Usual activities
0.950
No/slight problem
20
83.3%
21
84.0%
Moderate/Severe/extreme problem
4
16.7%
4
16.0%
Pain & discomfort
0.682
No/slight problem
17
70.8%
19
76.0%
Moderate/Severe/extreme problem
7
29.2%
6
24.0%
Anxiety & depression
0.957
No/slight problem
21
87.5%
22
88.0%
Moderate/Severe/extreme problem
3
12.5%
3
12.0%
Index
24
0.92
0.26
0.86
0.16
25
0.88
0.16
0.83
0.19
0.471
VAS
24
80.00
20.00
78.54
17.60
25
75.00
15.00
73.00
14.93
0.240
KHQ
Part I
General health perception (0-100)
24
25.00
12.50
30.21
23.29
25
25.00
25.00
31.00
20.77
0.900
Incontinence impact (0-100)
24
33.33
33.33
45.83
21.56
25
33.33
33.33
49.33
25.68
0.609
Part II
Role limitations (0-100)
24
16.67
33.33
20.14
23.04
25
33.33
33.33
30.67
23.90
0.123
Physical limitations (0-100)
24
16.67
33.33
22.92
22.42
25
33.33
33.33
32.67
24.76
0.156
Social limitations (0-100)
24
0.00
5.56
5.56
10.87
25
0.00
11.11
8.22
20.98
0.581
Personal relationships (0-100)
16
0.00
0.00
0.00
0.00
16
0.00
0.00
5.21
11.74
0.086
Emotions (0-100)
24
11.11
22.22
12.50
14.40
25
11.11
22.22
16.44
20.06
0.435
Sleep/energy (0-100)
24
16.67
33.33
27.08
31.01
25
33.33
33.33
37.33
31.28
0.255
Severity measures (0-100)
24
25.00
16.67
26.39
17.66
25
33.33
25.00
37.33
20.99
0.055
Part III
Symptom severity scale (0-30)
24
6.00
4.00
6.38
2.93
25
10.00
4.00
9.04
3.51
0.006
ICIQ-UI SF
Scale (0-21)
24
4.50
4.00
5.38
2.83
25
9.00
5.00
7.76
4.08
0.022
GSE-UI
Scale (0-120)
24
94.50
31.00
89.13
23.86
25
67.00
34.00
69.08
25.46
0.007
HADS
Anxiety scale (0-21)
24
5.00
6.00
5.13
4.59
25
7.00
5.00
7.80
4.65
0.049
Normal
19
79.2%
16
64.0%
0.593
Mild
2
8.3%
4
16.0%
Moderate
2
8.3%
2
8.0%
Severe
1
4.2%
3
12.0%
Depression scale (0-21)
24
2.00
3.50
3.08
3.28
25
3.00
3.00
3.44
3.92
0.732
Normal
21
87.5%
22
88.0%
0.720
Mild
2
8.3%
1
4.0%
Moderate
1
4.2%
1
4.0%
Severe
0
0.0%
0
T-tests for continuous variables and chi-square tests for categorical variables VAS Visual Analogue Scale, KHQ King’s Health Questionnaire, ICIQ-UI SF International Consultation on Incontinence Questionnaire – urinary incontinence short form, GSE-UI Geriatric Self-Efficacy index for urinary incontinence, HADS Hospital Anxiety and Depression Scale
The effect of the self-management intervention on outcome measures between intervention and control groups were demonstrated in Table 4. The difference captured on each outcome measure was further shown in Figs. 1, 2, 3,4, 5, 6, 7, 8 and 9, respectively. Participants’ general quality of life were improved within both groups after the follow-up, however no significant difference was identified (see Figs. 1 and 2). Similarly, no difference was shown in UI specific quality of life (see Figs. 3 and 4), self-efficacy (see Fig. 7), or depression status (see Fig. 9) between groups. However, significant differences were detected in participants’ KHQ symptom severity (− 1.77, p = 0.025; also see Fig. 5), ICIQ-UI SF symptoms scale (− 1.87, p = 0.031; also see Fig. 6), and their anxiety status (− 2.31, p = 0.001; also see Fig. 8), respectively. A positive trend was also observed in the participants’ KHQ personal relationships (− 3.89, p = 0.088; also see Fig. 4).
Table 4
Mean, standard error (SE) and p-values of pre-post intervention differences and treatment effect
Variable
Dimensions
Baseline differencea
Follow-up differencea
Treatment effectc
ORb/Coef.
SE
p-value
ORb/Coef.
SE
p-value
ORb/Coef.
SE
p-value
EQ-5D-5L
Mobility
No/slight problem
Moderate/Severe/extreme problem
1.33
0.92
0.675
0.57
0.45
0.481
0.32
0.33
0.267
Selfcare
No/slight problem
Moderate/Severe/extreme problem
Usual activities
No/slight problem
Moderate/Severe/extreme problem
1.38
1.02
0.663
1.05
0.81
0.950
0.74
0.77
0.774
Pain & discomfort
No/slight problem
Moderate/Severe/extreme problem
1.84
1.12
0.317
1.30
0.85
0.683
0.63
0.62
0.637
Anxiety & depression
No/slight problem
Moderate/Severe/extreme problem
0.63
0.46
0.526
1.05
0.91
0.957
1.24
1.14
0.811
Index
0.02
0.05
0.643
0.04
0.05
0.471
0.02
0.03
0.540
VAS
7.27
6.35
0.258
5.54
4.66
0.240
3.82
4.51
0.402
KHQ
Part I
General health perception (0-100)
1.33
5.35
0.804
-0.79
6.30
0.900
-1.63
5.38
0.763
Incontinence impact (0-100)
-11.11
6.44
0.091
-3.50
6.79
0.609
3.07
6.26
0.626
Part II
Role limitations (0-100)
-13.19
6.66
0.054
-10.53
6.71
0.123
-1.06
4.96
0.831
Physical limitations (0-100)
-7.75
6.17
0.216
-9.75
6.76
0.156
-3.82
4.96
0.446
Social limitations (0-100)
-7.42
5.64
0.195
-2.67
4.80
0.581
1.66
3.61
0.648
Personal relationships (0-100)
-6.35
7.37
0.396
-5.21
2.93
0.086
-3.89
2.19
0.088
Emotions (0-100)
-0.93
5.09
0.856
-3.94
5.01
0.435
-3.44
3.24
0.294
Sleep/energy (0-100)
-9.83
8.67
0.263
-10.25
8.90
0.255
-3.68
6.92
0.598
Severity measures (0-100)
-14.64
6.44
0.028
-10.94
5.55
0.055
-1.36
3.86
0.725
Part III
Symptom severity scale (0-30)
-1.92
1.21
0.119
-2.67
0.93
0.006
-1.77
0.76
0.025
ICIQ-UI SF
Scale (0-21)
-1.06
1.18
0.374
-2.39
1.01
0.022
-1.87
0.84
0.031
GSE-UI
Scale (0-120)
27.20
6.11
0.000
20.05
7.05
0.007
-4.90
5.16
0.348
HADS
Anxiety scale (0-21)
-0.44
1.38
0.755
-2.68
1.32
0.049
-2.31
0.66
0.001
Normal
Ill
0.92
0.53
0.879
0.47
0.31
0.245
0.34
0.28
0.188
Depression scale (0-21)
-0.21
1.05
0.840
-0.36
1.03
0.732
-0.17
0.46
0.715
Normal
Ill
2.30
2.11
0.364
1.05
0.91
0.957
0.44
0.54
0.505
VAS Visual Analogue Scale, KHQ King’s Health Questionnaire, ICIQ-UI SF International Consultation on Incontinence Questionnaire – urinary incontinence short form, GSE-UI Geriatric Self-Efficacy index for urinary incontinence, HADS Hospital Anxiety and Depression ScaleaDifference=intervention-control; bOR: odds ratio; cFor each outcome, analysis of covariance (ANCOVA) model with the baseline outcome was used to estimate the treatment effect
Fig. 1
Mean (95 and 90% confidence intervals) of pre-post intervention differences and treatment effect for EQ-5D
Fig. 2
Mean (95 and 90% confidence intervals) of pre-post intervention differences and treatment effect for EQ-5D utility and VAS scores
Fig. 3
Mean (95 and 90% confidence intervals) of pre-post intervention differences and treatment effect for KHQ, Part I
Fig. 4
Mean (95 and 90% confidence intervals) of pre-post intervention differences and treatment effect for KHQ, Part II
Fig. 5
Mean (95 and 90% confidence intervals) of pre-post intervention differences and treatment effect for KHQ, Part III
Fig. 6
Mean (95 and 90% confidence intervals) of pre-post intervention differences and treatment effect for ICIQ-UI SF
Fig. 7
Mean (95 and 90% confidence intervals) of pre-post intervention differences and treatment effect for GSE-UI
Fig. 8
Mean (95 and 90% confidence intervals) of pre-post intervention differences and treatment effect for HADS, Anxiety
Fig. 9
Mean (95 and 90% confidence intervals) of pre-post intervention differences and treatment effect for HADS, Anxiety
×
×
×
×
×
×
×
×
×
The relationship between the participants’ perceived improvement and the difference in outcomes within the intervention group was assessed using Spearman correlations (Table 5). There was a significant correlation shown between PGI-I and GSE-UI (rs= 0.43, p < 0.05). Mean change in GSE-UI for participants who responded “better” on the PGI-I were significantly higher than those who responded “no change” or “worse”.
Table 5
Correlation between PGI-I and changes in outcomes within intervention group
Mean change (SD)
PGI-I
Spearman's correlation
Very much worse
Much worse
A little worse
No change
A little better
Much better
Very much better
0 (0%)
0 (0%)
4 (16.7)
3 (12.5)
9 (37.5)
7 (29.2)
1 (4.2)
EQ-5D-5L
Index
NA
NA
0.03 (0.10)
0.08 (0.01)
0.05 (0.09)
0.05 (0.14)
0.00 (.)
-0.05
VAS
NA
NA
2.50 (16.58)
8.33 (23.63)
13.89 (18.33)
2.86 (14.39)
-15.00 (.)
-0.04
KHQ
Part I
General health perception (0-100)
NA
NA
12.50 (43.30)
8.33 (14.43)
-8.33 (17.68)
-14.29 (13.36)
25.00 (.)
-0.25
Incontinence impact (0-100)
NA
NA
-8.33 (16.67)
0.00 (33.33)
7.41 (27.78)
-4.76 (12.60)
0.00 (.)
0.05
Part II
Role limitations (0-100)
NA
NA
-8.33 (9.62)
5.56 (9.62)
-0.00 (18.63)
2.38 (17.82)
0.00 (.)
0.15
Physical limitations (0-100)
NA
NA
8.33 (28.87)
0.00 (16.67)
1.85 (15.47)
-4.76 (8.13)
-16.67 (.)
-0.19
Social limitations (0-100)
NA
NA
-5.56 (6.42)
0.00 (0.00)
-0.62 (14.28)
-7.94 (12.36)
0.00 (.)
-0.05
Personal relationships (0-100)
NA
NA
-16.67 (16.67)
0.00 (.)
0.00 (0.00)
-6.67 (14.91)
0.00 (.)
0.29
Emotions (0-100)
NA
NA
-11.11 (20.29)
0.00 (0.00)
-3.70 (9.62)
-6.35 (8.74)
22.22 (.)
0.08
Sleep/energy (0-100)
NA
NA
-4.17 (20.97)
-22.22 (9.62)
-7.41 (23.73)
-21.43 (20.89)
50.00 (.)
-0.02
Severity measures (0-100)
NA
NA
-12.50 (4.81)
-22.22 (17.35)
-3.70 (10.30)
-4.76 (13.49)
0.00 (.)
0.38*
Part III
Symptom severity scale (0-30)
NA
NA
-1.25 (6.50)
0.00 (4.36)
-1.89 (3.92)
-2.43 (3.78)
0.00 (.)
-0.13
ICIQ-UI SF
Scale (0-21)
NA
NA
-2.75 (2.22)
-1.33 (4.51)
-3.89 (3.66)
-3.86 (4.34)
-1.00 (.)
-0.02
GSE-UI
Scale (0-120)
NA
NA
-15.00 (17.03)
0.67 (11.02)
8.78 (9.87)
10.71 (15.64)
4.00 (.)
0.43**
HADS
Anxiety scale (0-21)
NA
NA
-1.75 (0.96)
-0.67 (1.53)
-1.11 (1.96)
-4.14 (3.34)
0.00 (.)
-0.22
Depression scale (0-21)
NA
NA
-1.00 (1.63)
0.33 (0.58)
-0.56 (1.88)
-0.86 (2.12)
0.00 (.)
-0.02
PGI-I Patient Global Impression: Improvement, VAS Visual Analogue Scale, KHQ King’s Health Questionnaire, ICIQ-UI SF International Consultation on Incontinence Questionnaire – urinary incontinence short form, GSE-UI Geriatric Self-Efficacy index for urinary incontinence, HADS Hospital Anxiety and Depression Scale**p < 0.05; *p < 0.1
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Qualitative findings
Individual interviews were undertaken with 15 participants from the intervention group at their homes. Participants ranged in age from 55 to 86 years. The majority were retired (11; 73%) and had suffered from UI for more than 5 years (11; 73%), but had received no support (13; 87%) from health services.
Each interview lasted between 15 and 48 min. A total of four themes were generated. Facilitators and barriers to the use of the self-management package followed by suggestions were also explored under each theme.
Raising awareness and gaining/refreshing knowledge
All participants found that this package had raised their attention to UI management as well as the resources and support available. Some participants learned new knowledge and management skills, while others found it useful to help refresh their memory. Positive comments were received on the fact that this package gathered both information and practical skills in a systematic and structured manner, accompanied by tips shared by women and health professionals.
“Yeah, I found the information on how to do the pelvic floor muscle exercises really good, it describes exactly what you should do and how much you should do..” (W5)
A few participants also expressed the need for more detailed information and tips to meet their needs. For instance, information and explanation were desired for biofeedback, vaginal cones, pads and how certain lifestyles impacted on UI symptoms and severity. In addition, some participants shared strategies and experiences of managing UI, including yoga, weight management programmes, and using reminders to practice PFME.
Half of the participants also identified the bladder diary as a potential barrier to the use of this book. For people who were in employment or regularly involved in outdoor activities, they felt that it was difficult and infeasible to measure intake of fluids and volume voided.
Feeling more confident and motivated to management UI
Participants generally felt more equipped and confident in managing their UI with resources and support supplied in the package.
“…we can do this, at least we know where to contact, we can tell the doctors also but if it happens to somebody you can tell them and they can do this.”(W24)
Participants also expressed their desire to motivate for self-management, however many of them did not practice as much as they would like to due to other commitments. Hence they suggested the inclusion of information and strategies on how to stay motivated and develop adherence.
“I suspect a lot of people would read the book, and think, oh yeah, that’s a really good idea, I ought to be doing that, and then never, ever actually do it.”(W46)
Being a useful and user-friendly package
All participants preferred the fact that this package was colour coded, making it easy to read and follow. They found the texts being easy to read and understand and the illustrations being appropriate, indicating that there was no need to book the support session. Some participants described benefit gained as a result of using this package.
“The book was very well put together, and very clear, very easy to read, and it was very informative.” (W6)
“I’m still having the occasional accident, but now I’m sort of going oh well, I will get there. It’s not a major setback. But it’s not affecting my life like it used to.” (W5)
Some of them preferred a smaller size of the package so they could carry in their handbags, whereas some believed that people tended to put it away if it was a small book. A few concerned about the phrase “older women” used in the title of the package and suggested to remove it or simply indicate “women over 55”.
Exploring dissemination strategies
All participants found the self-reported questionnaires in the feasibility study acceptable and considered them being necessary. Some appreciated being involved in this study. All participants recommended places where appropriate to distribute the package, including doctor’s surgeries, hospitals, pharmacies, workplaces, public libraries, local leisure centres, and other meeting places for women.
Some participants also expressed the need to design the package in multiple languages groups who may have limited access to support and resources. In addition to delivering the package to individuals, a couple of participants expressed their preference for a group to enable peer support.
Discussion
This results of this study provide supporting evidence for the feasibility and acceptability of the self-management package as a complementary strategy for the management of UI in older women. This results of the feasibility RCT have confirmed that recruitment of women with UI from local community centres who were not actively engaged with health services is feasible and the drop-out rate is low. Completion and follow up of the questionnaires were successful. The findings of the acceptability study have suggested that the package may be a useful resource in improving women’s knowledge and practical skills for the management of UI. Women also expressed the need for such intervention for this condition and commented that questionnaires used to capture information were acceptable.
The feasibility RCT showed that women’s UI severity, symptoms and anxiety status were improved after the intervention for 3 months. This provides initial evidence that this self-management package has the capacity to reduce both physical and emotional impact of UI on women. There is an increasing interest in the self-management of UI consisting in both research and practice, however many interventions only focused on one particular skill or technique [6]. The UK Continence Society has recommended a support package for patients with UI as a minimum standard for continence care [41]. With no evidence-based package being available, this study developed the intervention consisting of multiple components and also demonstrated the acceptability of the intervention and potential benefit on women’s physical and psychological health. Therefore, future studies are needed to evaluate the intervention in other settings in a larger multicentre trial in order to gain robust evidence.
Although the difference in women’s quality of life or self-efficacy was not detected, women described that they felt more confident and motivated to self-manage their condition and some of them gained improvement after using the package. Qualitative interviews further supported these findings and participants reported that the package was informative and useful in raising their awareness. A significant correlation was observed between women’s self-efficacy and their subjective perception of improvement. This suggests that women who gained a higher level of self-efficacy were likely to experience an improved subjective perception of their UI condition. Therefore, individual’s self-efficacy level needs to be assessed as a way to stratify participants before randomisation process. For those with extremely low self-efficacy, interventions with a purpose to build their confidence may be needed before providing self-management package.
Existing literature has shown modest benefit of self-management interventions in older women with UI. Compared to pharmacological therapies alone, nonpharmacological interventions, such as behavioural therapy either alone or combined with other intervention, are more effective in achieving cure or improvement both stress and urge UI [42]. Clinical effectiveness of self-management of UI has also been with respect to symptoms, UI severity, quality of life and perceptions of improvement when being delivered in group format with effects maintained (12 months [43]. Similarly, this study has observed improvement in symptoms and severity with the self-management package, and effects on psychological health. This package appears feasible to modify women’s quality of life living with UI. Further studies may be needed to investigate the effectiveness of self-management interventions on both physical and psychosocial outcomes in women with UI, at both short and long term.
Strengths and limitations
The intervention was co-developed with key stakeholders including women with UI and health professionals. The feasibility and acceptability of the intervention were evaluated with women who were not actively engaged with clinical services for UI. Potential positive effects were observed in women’s UI symptoms and their psychological status, which were further supported by the women’s experiences. However, careful interpretation is needed. The study was not allocation concealed and the sample size was not sufficiently powered to make robust inferences about the effectiveness of the intervention. Further studies are needed with a large sample size in multiple clinical settings to evaluate the effectiveness of this package. There is a possibility of bias associated with the self-reported measures. Objective information such as pad test or measure of PFM strength may be needed. It is worth noting that pad tests are not recommended in the routine assessment of women with UI by the NICE [44]. Also, women may be less in favour of the invasiveness of the measures such as vaginal dynamometer.
Conclusions
The self-management package consisting of multifaceted behavioural techniques appears feasible to improve UI symptoms, severity and anxiety status in older women living with UI. Women also found it useful for increasing their awareness, motivation and knowledge of UI management. This study suggested that this package has the potential to be implemented in routine practice with further evaluation of effectiveness in clinical settings.
Acknowledgements
We thank women and health professionals’ involvement and their contribution to this study.
Ethics approval and consent to participate
Ethics approval was granted by the School of Healthcare Research Ethics Committee (HREC 18–001) at the University of Leeds, UK. All of the data were collected with the written informed consent of participants provided prior to the study.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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