Background
Recovery
Objectives
Method
Stage 1
Stage 2
Stage 3
Inclusion criteria: | Exclusion criteria: |
---|---|
Target group | |
Individuals with long term mental health problems Individuals > 18 years old | Individuals with substance abuse problems only |
Intervention | |
Internet based; web-pages and applications for computers, smart phones and tablets | Solely phone calls, text messaging, voice response or videoconference |
Part of ongoing treatment and care | Stand-alone interventions |
Support for recovery-oriented practices as described by the interventions’ aims and components | Solely support for • self-guidance • monitoring • managing care |
Study design | |
All study designs, including development reports | Editorials/comments, reviews |
Type of publication | |
Published in peer-reviewed journals | Gray literature |
Language | |
English or Scandinavian | Non-English and non-Scandinavian |
Stage 4
Stage 5
Results
Characteristics of the e-recovery interventions
Intervention and origin | Aim | Target group and setting | Modules |
---|---|---|---|
CommonGround, USA | Recovery and shared decision-making | For persons 18 years or older with severe and persistent mental illness at an outpatient psychiatric medication clinic. | A program consisting of a peer-to-peer workshop and training of providers in addition to a peer-run center including a software program: written material and videos with peers describing their recovery process; reminders of their own actions that give their life meaning and purpose and help to create wellness; a customized survey of symptoms and psychosocial functioning and primary goals for the medication visit; a database; a recovery library; and a one-page report to use in the medication visit. |
Horyzons, Australia | Recovery and maintaining clinical benefits | For persons aged 15–25 years with first episode psychosis following discharge from early intervention specialist care in consultation or at home. | A moderated online social networking forum: evaluation of service users’ goals, recovery style, and symptoms; interactive information on psychosis and the recovery process with emphasis on empowerment and social recovery; assessment of strengths; identification of early warning signs and a relapse prevention plan; interactive exercises about activity; cognitive-based strategies; and general overview of the key aspects of the completed modules with an emphasis on personal achievement and recommendation to stay well and to use the social networking features and practice personal strengths. |
Miele.Neta, Finland | To support self-management | For persons aged 18–65 years with schizophrenia spectrum psychoses in inpatient and outpatient settings. | Service user education and online support: information about illness, treatment, well-being, daily activities, and service users’ rights; a channel for peer support; recordings of voices telling service users’ life stories; drawings and pictures; a diary; eSupport; a tool for counseling; and interaction between service users and providers. |
ReConnectb, Norway [55] | Greater overview and control regarding health and well-being, legitimacy of personal knowledge, strengths and values, and a sense of continuity in relationships | For adult persons with long term mental health problems at different levels of mental health care. | An intervention for guided self-help where service users can: state their values and what is important in their life; describe their current situation, goals and activities related to a wide range of domains; do exercises related to coping strategies, strengths, collaboration with providers, and lifestyle; write a crisis management plan; register information about various aspects of daily life such as sleep, nutrition, physical activity, social life, and medications; get information on issues related to daily life, health, well-being, and social activities including material from peers; register information related to medication; and get access to secure email with their providers. |
Wegweis, The Netherlands | Shared decision-making and individual advice related to treatment, rehabilitation, and personal recovery | For persons 18–65 years with schizophrenia or related psychotic disorder for use at home or in a clinical setting. | An Internet-based information and decision tool providing service users: results of their routine outcome monitoring assessments and personalized advice; descriptions of treatment modules dynamically linked to the assessment results; and overview of available treatment modules. Advice is based on evidence-based information, clinical expertise, and service users’ experiences and also refers to the service user’s provider and local counselor. |
Your Schizophrenia Care, USA [90] | To empower service users to discuss their mental health treatment with their provider | For adult persons with schizophrenia in outpatient mental health care. | A service user-oriented learning approach related to six areas of quality of care: medications, side effects, referrals, family support, employment, and quality of life. Based on service user’s input on their current status and treatment related to each area, individualized feedback recommendations appear on the screen. The Web site includes video clips designed to model communication strategies and skill, and show how to be proactive in a visit, e.g., by expressing expectations and goals. Service users are encouraged to discuss their responses with their provider in an upcoming visit. |
How recovery is supported though the Internet interventions
Promoting citizenship
Organizational commitment
Personally defined recovery
Working relationship
Characteristics of the studies
Study | Aim | Methods and outcome measures | Main findings |
---|---|---|---|
CommonGround [53] | To describe challenges in decisions about medications and the CommonGround program | Reflections and descriptions based on lived experience and research. | Program being piloted. Promising as support for shared decision-making, decisional conflict and optimizing activities that give life meaning and purpose in recovery. |
CommonGround [54] | To describe a 12-month pilot for shared decision-making in psychopharmacology consultation | Observational record for each use of the software from two case management teams for a total of 189 clients. Focus groups with case managers (n = 14) medical staff (n = 4), clients (n = 16) and peer-specialist staff (n = 3). | The software was used 662 times varying from one to ten times for each client. Only ten clients refused to use it at some point. The intervention helped practitioners focus on client concerns, enriched dialogue and understanding, made the consultations more effective and empowered client involvement in decision-making. |
CommonGround [81] | To describe CommonGround, new role for peers and early adopters, patterns of use and lessons learned | Use of CommonGround database and observation of 8 sites already offering the tool to a total of 4783 users. Log files of use by clients, peers, administrators, therapists, and case managers. | Technology and peer support can enhance shared decision-making even during brief (15-min) psychiatric medication consultations. |
CommonGround [49] | Examine the impact of a decision support center and computerized tool on adherence to psychotropic medication | Multivariate linear regression models were used to examine if tool users (n = 122) had higher rates of 180-day medication adherence than non-users (n = 1000) based on administrative pharmacy claims data. | Relatively good adherence for psychotropic medications at baseline. Intervention had no detectable impact on adherence rates. |
CommonGround [82] | To describe the use of self-management strategies, especially a strategy called “Personal Medicine” and how it correlates with wellness and symptom improvement | Pretest-posttest single-group design. A retrospective study of responses from CommonGround health reports generated from 12 clinics and service users (N = 5584). A self-developed questionnaire. | Health functioning improved with time. Self-management reduced medication side-effects, increased user satisfaction with medication, and fostered recovery. |
CommonGround [83] | Examine the impact of CommonGround on the consumer–doctor interaction in medication consults | Pretest-posttest control group design for four months (N = 98). Measure of Patient-Centered Communication (MPCC) and Patient Perception of Patient-Centeredness (PPPC). | No significant effect at baseline. Improved scores after four to six months suggest need for longer intervention and better fidelity. |
Horyzons [84] | To describe the rationale and potential of moderated online social therapy and examine the acceptability, safety and initial clinical benefits of system | A six-week trial using an uncontrolled single-group design for participants with first episode psychosis (N = 20) participating at least four weeks. Descriptive statistics of log files of use. A questionnaire and semi-structured interviews. Structured Clinical Interview for DSM-IV (SCID patient version), Brief Psychiatric Rating Scale (BPRS), the Calgary Depression Scale for Schizophrenia (CDSS) and the Beck Anxiety Inventory (BAI). | No drop-outs; 70% used the system > three weeks, 95% used social networking, and 60% completed > three modules. The majority of participants reported feeling safe, empowered and more socially connected; 70% considered it a useful post-treatment option. Depressive symptoms were significantly reduced at follow-up. |
Horyzons [85] | To assess the safety of Horyzons | Semi structured interviews with participants and simple descriptive statistics from online posts and interviews. Structured Clinical Interview for DSM-IV (SCID patient version) and Brief Psychiatric Rating Scale (BPRS). | No clinical or security problems were noted. Users felt safe using Horyzons. |
Horyzons [65] | To determine design guidelines for increasing engagement in mental health applications | Complex health intervention framework in stages: theory, design, exploratory trial, and implementation. | Themes identified for use in guidelines: 1) belonging and security, 2) better understanding of condition, 3) engendering positive thoughts, being accountable and focusing on strengths, and 4) appealing and engaging presentation. |
Mieli.Neta [86] | To evaluate usability, quality, functionality, content and benefits of Mieli.Net | Explorative descriptive multiphase study among nurses (N = 76), using a questionnaire (The Quality Criteria of Public Online Services) and descriptive statistics, and additionally written feedback and content analysis. | The evaluation showed good portal functionality, relevant content and benefits for users. |
Mieli.Neta [52] | Identify barriers and facilitators in implementation of Mieli.Net | Questionnaire after one year use of portal among nurses (N = 89). Two thematic open-ended questions analyzed by using content analysis. | Issues emerged in four categories: organization resources, nurses’ individualities, patient-related factors, and portal-related factors. Barriers: lack of computers, time and/or training; nurses’ negative attitudes. Facilitators: easy access to technical resources and Internet; time and motivation among staff. |
Mieli.Neta [50] | To describe the design and development process of Mieli.Net | Mixed methods design in four phases: needs analysis (survey for administrative personnel (n = 36) and patients (n = 316), interviews with patients (n = 51) and relatives (n = 50) and overview of the literature); development of information areas (relevant literature and feedback from multidisciplinary team and end-users); development of a prototype (information source from 10 focus groups meetings and existing computer-based support systems; and evaluation by clients (n = 21), nursing students (n = 20) and nurses (n = 35). | Five informational areas were identified: illness, treatment, well-being, daily activities, and patient’s rights. Based on this, changes were made in the structure and new applications were added. The service was found to be promising. User involvement in development is important. |
Mieli.Neta [87] | To describe nurses’ experiences of information technology-based standardized patient education | Nurses completed a questionnaire about their experiences (n = 56), analyzed by content analysis. | The intervention brought the patient and the nurses closer to each other and helped nurses to provide individual support for their patients. The education was time-consuming. |
Mieli.Neta [88] | To determine the effectiveness of a needs-based computerized patient education program on patients’ experience of being deprived of their liberty during hospitalization | RCT with three groups: an intervention group with needs based computerized patient education (n = 100), a patient education group with conventional education (n = 106), and a control group with standard care (n = 105). Primary outcome measure patients’ self-reported deprivation of liberty developed for the study, and additionally the PSS-Fin (patient satisfaction scale, Finnish adaptation). | Technology-based education was not found to be superior to other approaches. |
Mieli.Neta [89] | To compare user groups’ evaluation of usability | Descriptive design, a small-scale usability study with service users (n = 21), nursing students (n = 21) and registered nurses (n = 35). A self-developed questionnaire about the content, structure and visual appearance of the website. | Service users were positive to intervention tools, but require support. Content, structure and appearance rated as good. |
ReConnectb [55] | To describe the design and development process | Community-based participatory research design with particular focus on implications of service user involvement, conducted in two communities by a practice-research-team, involving work-shops with stakeholders and an iterative design process. | The intervention invites a proactive approach from providers. Service users must be involved at all levels of project development to promote person-centeredness. |
Wegweis [51] | To investigate the usability of web-based support for routine outcome monitoring (ROM) | A usability study consisting of three types of evaluation; heuristic, qualitative and quantitative with service users (n = 15) and ICT experts (n = 4). Usability testing grouped into usability topics, verbal reports and observations. Questionnaires . | The prototype has promise for improving ROM practice. Study confirms earlier findings that people with psychotic disorders are not incapable of using web-based systems independently. |
Wegweis [64] | To present, evaluate and explain the shared decision support module in Wegweis | An ontology-based approach for selecting and ranking information for service users with schizophrenia based on their routine assessment results. The Manchester short assessment of quality of life (MANSA). | Wegweis pioneers automated interpretation of assessment of results for service users with schizophrenia. Tool interpretations corresponded well with those of clinicians. Service users considered most of the automatically generated advice relevant. The tool is deemed feasible. |
Wegweis [56] | To investigate the intervention in naturalistic setting | An open-label, 2-group, parallel RCT with patients with psychosis (N = 250) recruited from two outpatient teams, and process evaluation with open interviews with patients (n = 15), observation of discussions, and a questionnaire among clinicians. Primary outcome: Combined Outcome Measure for Risk Communication and Treatment Decision-making Effectiveness (COMRADE). Secondary outcome: Client Satisfaction Questionnaire (CSQ). | Inconclusive results on service users’ satisfaction and involvement in decision-making. Poor provider adherence to the protocol may explain the lack of effect. Improved training of clinicians and adaptation of the intervention to the organization is recommended in future studies. |
Your Schizophrenia Care [90] | To test the hypothesis that patients assigned to the intervention would be more verbally active and that mental health providers would be more patient-centered in the visit | RCT with patients who have schizophrenia (N = 50). The visits were recorded and analyzed using the Roter Interaction Analysis System. Different variables related to communication (e.g., number of statements, patient-centeredness ratio and type of questions asked and information given) and affective tone during visits was measured. | Visits by patients in the intervention group were longer and had greater patient contribution to the dialogue than visit by the control group. Clinicians asked more questions about treatment and the condition than in the control group. |