Introduction Informal caregivers play a major role in the support and maintenance of community patients with severe psychiatric disorders. A pilot study showed that an individualised brief intervention such as the Ensemble programme leads to significant improvements in psychological health state and optimism.
Methods and analysis This randomised controlled trial aims to compare the efficacy of using Ensemble in improving informal caregivers’ psychological health states and the ability to play an active role in their situations with that of support as usual. Improvements on the psychological health global index will be measured three times (T0-pre, T1-post and T3 2 months follow) with standardised questionnaires (the Global Severity Index of Brief Inventory Symptoms, the Life Orientation Test-Revised, the 36-item Medical Outcome Study Short-Form Health Survey and the French Zarit Burden Interview). Differences between groups in post-test and pretest values will be examined using an analysis of covariance for each outcome variable. The severity of illness measured by the Social and Occupational Functioning Assessment Scale will also be collected at T0 and T2 to compare eventual patient improvements. At the end of the programme, the experiences of the 20 patients participating in the Ensemble programme will be evaluated qualitatively.
Ethics and dissemination The research protocol received full authorisation from the Human Research Ethics Committee of the Vaud state, Switzerland. The principal paper will concern the results of the experimental design used to test the Ensemble programme. The research team will prioritise open access publications.
Trial registration number NCT04020497
- primary care
- public health
- clinical trials
- rehabilitation medicine
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Strengths and limitations of this study
This is the first randomised controlled trial in Switzerland to test Ensemble, an active individualised programme for the informal caregivers of people suffering from a psychiatric disorder in comparison to controls.
The Ensemble programme is brief (five sessions, once a week), tailored and offers different practical tools for informal caregivers to improve their health, quality of life and ability to cope with the patient’s illness.
The intervention provider endorses a facilitator role to improve informal caregivers’ empowerment.
Tailored early interventions are recommended because actual support given in practice lacks consideration of the informal caregivers’ specific needs and should not depend on only the patient’s treatment.
No comparison with an active intervention (as a psychoeducation programme) presents a limitation.
Care in the community has greatly improved the conditions of people with severe and persistent mental disorders. In this context, informal caregivers are significant partners, and appropriate support must be provided.1 2 Although family and informal caregiver play a vital role in the early detection of mental health disorders and facilitating access to care, it is not easy for health professionals to develop such partnerships.3 Several studies have underscored the importance of supporting informal caregivers in their capacities to integrate their new caregiver’s role.4–6 Möller-Leimkühler demonstrated that informal caregivers need emotional support as soon as the diagnosis is made.7 Emotional support is essential in the moratorium stage of recovery.8 9 When a patient’s close informal caregiver first learns about a diagnosed psychiatric disorder, he or she might feel a range of emotions and might exhibit varied reactions linked to this stage (eg, revolt, confusion, hopelessness, denial). In the second stage of recovery, relatives develop a greater awareness of the disorder, although this awareness can raise significant fears about the future. Feelings such as guilt, avoidance or a desire to give up can emerge.8 9 It is, therefore, critical to intervene early during the first two stages of recovery to promote the health of informal caregivers and to reorient them away from unsuccessful coping strategies that might be harmful in the long term.8–10 Informal caregivers often feel helpless, lack confidence regarding how to help the sufferer and experience shock when faced with a close relative suffering psychologically.11 12 They can experience significant distress since they lack support and practical tools for managing the situation.4 Feelings of helplessness and uncertainty can be compounded by a lack of knowledge of the disorder and not knowing how to help the patient.13 Informal caregivers could become isolated due to the harmful effects of stigmatisation, which can also have negative impacts on their health.14 Indeed, informal caregivers of people with severe psychiatric disorders can experience serious situations with potential negative consequences for their quality of life, their own health and the health of the patient.15–17 In order to help them developing effective coping strategies, interventions must be contextualised, culturally adopted and specified to the informal caregiver’s role in order to fill individualised needs.18 19 These diverse issues are crucial for understanding how to better support informal caregivers. The results of a meta-analysis of patients suffering from schizophrenia spectrum disorders showed that most programmes include information about the disease and focus on the development of communication and coping skills to reduce the negative effects on caregivers.20 Interventions for bipolar disorder are mainly based on the ‘vulnerability-stress model’ and include information about how this illness impacts relatives, as well as training sessions on communication skills and problem-solving techniques.21 Interventions tested in a study of depressive disorders included theoretical input on aetiology, and they focused on the causes of depression, depressive symptoms, treatment and the development of coping strategies.22 Previous studies have also identified that informal caregivers need tailored knowledge of the patient’s illness, clarification of their roles and responsibilities, better control over their own lives and effective collaboration with health professionals.4–7 12 23 24 Additionally, scientific data recommend adjusting caregivers’ support according to the phase and severity of illness, as well as the caregiver’s sociodemographic characteristics.7 Most of the interventions published in the literature have focused on the ill family member and his or her support but not on the specific needs of informal caregivers as the core intervention. Lobban et al presented an individualised programme that is self-managed and specific for relatives of people with recent-onset psychosis.11 To reduce the gap between scientific recommendations and actual practice, a tailored intervention called Ensemble (Together in English) was developed and tested in a pilot study.3 25 The results of this pilot study showed that informal caregivers experience many difficulties and unmet needs regarding their caregiver role, as well as painful emotions, while having many social resources that are not specific to their individual needs. The participants had several difficulties in essential areas of life, such as family, children, romantic relationships and mental health. The needs of each caregiver differ between the participants which confirm the necessity of individualised support.3 Comparing Ensemble to psychoeducational programmes or counselling programme would involve tailoring the support to the need of each participant. The support sessions offer different practical exercises and tools (problem solving, positive communication and assertiveness, involvement as an informed caregiver, emotional support…), which need to be adapted to each participant.
Regarding the primary outcome of the Ensemble pilot study, the participants showed significant improvements in psychological health status as measured by the Global Severity Index (GSI), based on the Brief Symptom Inventory (BSI) scale.25 After five sessions, the 21 participants’ psychological health statuses were improved compared with their pretest scores (pretest mean of the GSI score 0.72 vs post-test GSI score mean 0.53). These findings emphasise that informal caregivers are at greater risk of developing psychological problems than those in non-clinical populations; for example, their mean GSI score pretest (0.72) was higher than that of a healthy British community sample (0.44)26 and lower than that of a British psychiatric outpatient sample (1.65).27 Informal caregivers were also more optimistic regarding their future at the end of the programme as a secondary outcome (mean pretest 15.52 vs mean post-test 17.43).
The goal of the current study is to determine whether the Ensemble programme is clinically effective using a randomised, controlled (RCT), and assessor-blinded trial. A combination of Ensemble plus support as usual (SAU) will be compared with SAU alone.
This trial’s main hypothesis is that five 1-hour sessions of the Ensemble programme will lead to an improved psychological health state, as evaluated with the GSI score on the BSI scale, compared with those of the control group. The secondary hypothesis is that the Ensemble programme will increase optimism levels as measured on the Life Orientation Test-Revised (LOT-R) scale, improve quality of life as measured by the Short-Form Health Survey (SF-36) scale and decrease the burden score on the Zarit scale. The study will also monitor the sustainability of the potential benefits at follow-up (2 months after completing the Ensemble programme). Qualitative data through 20 semioriented interviews will provide information on outcomes concerning the experience and the added value of the programme for participants at the end of the study.
A study summary according to WHO Trial Registration Data Set items is presented in table 1.
Participants, interventions, and outcomes.
The study is being conducted in four cantons of French-speaking Switzerland. Informal caregivers providing close support to persons with psychiatric disorders are the target population. ‘Informal caregiver’, ‘caregiver’ and ‘family caregiver’ are terms used to describe family members, friends or significant others who provide this close support. In this area, no systematic or standardised individualised intervention for informal caregivers is implemented. Several sites in these four cantons are informed, and different partners actively support this project (a detailed list can be obtained from the authors) to reflect generalisation issues. The main study site is La Source, School of Nursing Sciences, HES-SO University of Applied Sciences Western Switzerland, Lausanne. However, the research assessments and the meeting intervention can take place at the participants’ homes or in other locations defined as appropriate by the participants and intervention providers. The research members will travel up to 3 hours one way for these meetings and assessments.
The study is open to informal caregivers of adult psychiatric patients with a burden score of at least 20 on the French Zarit Burden Interview (ZBI) version scale.28 This 22-item scale uses a 5-point scale (0 = ‘never’; 4 = ‘nearly always’) to assess the subjective burden (emotional, physical and financial) of an informal caregiver of an individual with a loss of autonomy. The total score can range from 0 to 88. A score less than or equal to 20 indicates a low burden; a score between 21 and 40 indicates a light burden; a score between 41 and 60 indicates a moderate burden; and a score greater than 60 indicates a severe burden. The inclusion criteria for informal caregivers are as follows: being at least 18 years old; living in French-speaking Switzerland; speaking French and having an adult relative suffering from a psychiatric disorder (with or without an established diagnosis). One hundred and sixty participants will be included in this study (n=80 for Ensemble + SAU; n=80 for SAU). In this study, a self-report identification as informal caregivers is selected to offer support to all informal caregivers according to their needs independently of their direct implication in caregiving to patient.
Participants will be recruited from the following family associations in French-speaking Switzerland: l'Îlot (VD), AFS Berne-Neuchâtel (NE), A3 Jura (JU) and APF (FR). Participants will also be recruited at ‘l’Espace Proches’, which is a nonprofit association created in 2014 and a member of the Department of Health and Social Welfare and the Pallium Foundation. The services of this association are run by health and social professionals and focused on informing, orienting and supporting informal caregivers or relatives. Public mental health services will also be used to recruit participants. Meetings with the presidents of each association and professionals working in mental health services will be organised to present the project. Regular information about the research will be provided at these sites. A recruitment strategy aimed at general practitioners, local newspapers, schools and social and cultural centres, as well as social networks such as Facebook, will be deployed to ensure equivalent treatment among informal caregivers who are isolated or not in contact with any association. Informal caregivers who are willing to participate will choose either to call the research coordinator or give their authorisation to be contacted.
Patient and public involvement
No patient involved.
Ensemble is a brief individualised intervention designed to promote the well-being of informal caregivers who experience the effects of their patients’ psychiatric disorders. It is a five-session programme led by a nurse (who had 2 days of specific training), addressed to the informal caregiver and delivered independent of the patient’s treatment. Figure 1 demonstrates the objectives of the Ensemble programme and its process. The five sessions are described and allow the participant to take a step back on her/his informal caregiver’s role.
Three clinical tools are used to specifically assess the needs, difficulties, painful emotions and social networks of the informal caregivers (table 2). These clinical tools are systematic, structured and easy to administer. The three clinical tools selected in the Ensemble programme are (1) the Difficulties and Needs Self-Assessment Tool, (2) the Painful Emotions Tool and (3) the Social Network Tool.3 25 29 30
Support as usual
SAU was chosen as a control condition. Informal caregivers must often manage situations in different ways. SAU consists of informal support given by various structures. The patient’s clinical team can provide support to the informal caregiver. Specific psychoeducation programmes tailored to the patient’s illness (such as ‘Profamille’ for schizophrenia) are also implemented in the French-speaking Switzerland context. Peer support depends on the voluntary work of family associations. Some general professional services such as ‘l’Espace Proches’ focus on informing and orienting informal caregivers or relatives in the state of Vaud. No attempts have been made to standardise this treatment as SAU that depends on informal caregivers’ needs, knowledge of the health system and their capacity to be in contact with the patient’s psychiatric team.
Ensemble programme’s implementation
Three nurses are trained to deliver the programme. The training took 2 days and is organised in four sessions.
Session 1: issues concerning support for family caregivers, theoretical foundations of the Ensemble programme, professional posture and informal caregivers’ health considerations.
Session 2: Ensemble Programme: tailored support, structured and individualised process, assessment of difficulties and needs, painful emotions and social resources, practical training to use the clinical tools with a vignette designed from the pilot phase, issues concerning the awareness of the informal caregiver’s role.
Session 3: Practical exercises of the support tools—problem solving, positive communication and assertiveness, and involvement as an informed caregiver.
Sessions 4: Practical exercises of the support tools—emotional support, isolation and peer support, and referral to appropriate structures.
In addition to this training, nurses received a manual protocol and are supervised for every clinical situation. To ensure the standardisation on delivery, two supervisions moments are planned: the first after the first meeting between the nurse and the participants and the second before their last meeting. The place for delivery of the sessions are in a private and quiet room located to the nursing school, or in a clinical local or in the participant’s home. Sometime if the participant prefers the delivery could take place in the ‘tea-room or hotel’ but this option is retained only if the other options are not suitable for the participant.
Quantitative data gathered through various standard instruments will inform the main and secondary outcomes. Table 3 summarises the expected results.
Qualitative data will also inform some secondary outcomes. Content analysis will focus on not only informal caregivers’ experiences but also their capacity to manage the situation. To narrate their experiences and construct meaning through heuristic narrative processes,31 the analysis of the categorisation devices used by the participants will provide us with comprehensive insight into the types of experiences during the programme, different capacities and unmet needs.
The sample size was estimated using the results of the pilot study regarding the main outcome of the expected BSI Global Index. For the sample size calculation, α was set at 0.05 with a power of β=0.80. The effect size of the expected difference between the two groups was equal to Cohen’s d=0.470. Using an a priori computation for analysis of covariance (ANCOVA), the proposed trial required a total sample size of 144 participants for the two arms, 72 in each arm. In the pilot study, 1 of 22 participants dropped out, resulting in a dropout rate of approximately 5%; to increase security in the proposed study, a drop-up rate of 10% will be considered, corresponding to a dropout number of 22 participants, so the present study will recruit 160 participants. Between-group differences in pretest and post-test values will be examined using ANCOVA.
Participant timeline and RCT process
Figure 2 shows the clear and synthetic timeline of participant interactions and this RCT process.
The Research Electronic Data Capture (REDCap) platform will be used to randomise the participants. REDCap is a secure, web-based application designed to support data capture for research studies. It developed a module that allows a defined randomisation model be implemented within the project. The randomisation by group/site model was defined. A randomisation table was created by the data manager and imported to the project database to structure the allocation. REDCap will randomise the participants according to this table, which is not available to the research team. A total of 180 assignments in the allocation table were included to accommodate possible drop-outs and additional enrolment of participants.
A person not involved in the execution of the project will confirm that the eligibility data are complete in order to proceed with the randomisation. She/he will then inform the intervention provider of the allocated arm.
The intervention provider will inform the participants whether they are in the intervention arm, but the assessor will not be informed of hers/his treatment group allocation.
The role of the assessor is to ensure the connection to the REDCap platform that holds the research questionnaires. The assessor responds to eventual questions about item understandings during the assessment. The assessor is blind and reminds the participant not to communicate hers/his treatment group allocation at the beginning of every encounter at T1 and T2. The assessor will also collaborate with one of the investigators at the end of the study to collect qualitative data.
The research assistants will alternatively play the role of either the assessor or the intervention provider to diversify their work and develop specific competences related to each role. To maintain blindness of assessment, several conditions have been set: one assistant researcher will take the role of assessor for the first five participants before providing the intervention for the next five. Another assistant researcher will do the opposite and so on. If a leak of allocation occurs, this information will be noted, and analyses concerning the eventual impacts will be conducted. However, all standardised questionnaires are basically self-administered.
The interventions will take place in a building other than the assistants’ office. The supervision between interventions will be individualised and organised by one of the two lead investigators.
Data collection, management and analysis
Study data will be collected and managed using REDCap electronic data capture tools hosted at HES-SO Fribourg. REDCap provides (1) an intuitive interface for validated data entry; (2) audit trails for tracking data manipulation and export procedures; (3) automated export procedures for seamless data downloads to common statistical packages and (4) procedures for importing data from external sources.
The BSI aims to assess psychological symptoms and psychological distress. It includes 53 items organised into 9 primary and clinically relevant symptom dimensions: (1) somatisation; (2) obsessive–compulsive; (3) interpersonal sensitivity; (4) depression; (5) anxiety; (6) hostility; (7) phobic anxiety; (8) paranoid ideation and (9) psychoticism.32 This scale also has three global distress indices: the GSI, the Positive Symptom Distress Index and the Positive Symptom Total. The BSI scale has been used in a variety of clinical and counselling settings as a screening tool for mental disorders and as a method of measuring symptom reduction.33–36 It has also been used to assess the psychological health status of informal caregivers.25 37 38 The GSI of the BSI scale was used as one of the main outcome measures in the pilot study and represents the mean of the nine primary symptom dimensions and is more sensitive than the two other global indices.32 Higher GSI scores indicate a greater effect on informal caregivers’ psychological health. The validation of the French BSI scale indicated good internal consistency for the GSI score (α=0.91).39
The French ZBI includes 22 items to assess the subjective burden (emotional, physical and financial) of an informal caregiver of an individual with a loss of autonomy.28 The total score can range from 0 to 88. A score less than or equal to 20 indicates a low burden; a score between 21 and 40 indicates a light burden; a score between 41 and 60 indicates a moderate burden and a score greater than 60 indicates a severe burden. This questionnaire has been mainly used for chronic illnesses such as dementia, palliative care or mental disorders.40–42
The LOT-R developed by Scheier et al43 measures an individual’s optimism regarding a given situation. This self-administered scale measures the adaptive strategies correlated with well-being and is used to evaluate optimism vs pessimism. The LOT-R has been translated and validated in French, with good psychometric proprieties (internal consistency α=0.76).44 The scale includes 10 items: three items measure optimism, three others measure pessimism and four items function as fillers. The participants respond to each item on a 5-point Likert scale ranging from0 (strongly disagree) to 4 (strongly agree); the four filler items are not included in the total score calculation. Higher scores suggest more optimism. Optimism has been shown to be negatively correlated with distress45 46 and to positively influence quality of life.47 Among informal caregivers in particular, optimism promotes engagement in supportive programmes,48 whereas pessimism leads to the use of avoidance strategies, which can predict informal caregiver burden.49
The 36-item Medical Outcome Study SF-36 developed by Ware and Sherbourne50 measures some health indicators related to quality of life. It includes 36 items and is used in clinical and general population settings to evaluate eight health dimensions: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue and general health perceptions. Two global scores— (1) a Physical Component Score and (2) the Mental Component Score – are obtained by grouping the eight dimensions, and these two synthetic variables allow different populations to be compared. The French version of the SF-36 was validated by obtaining Cronbach’s (reliability) coefficients ranging from 0.76 to 0.92.51–54 In clinical settings, this type of measure can also help professionals orient informal caregivers towards a targeted intervention.55 56
The different standard measures will be used in the three standard evaluations (T0=pretest; T1=post-test at an average of 2 months and T2=follow-up at an average of 4–5 months). A research assistant trained to answer technical questions will be present during the questionnaire’s completion.
The Social and Occupational Functioning Assessment Scale (SOFAS) developed by Goldman et al57 is used in order to reflect the severity of the patient’s illness in the professional and social functioning. This scale does not consider the psychiatric symptoms’ severity. It is a continuous scale (0–100) which present 10 functioning level, each level is described by a short text. A higher level (91 to 100) shows a more superior social and occupational functioning. This scale is validated in French (coefficients ranging from 0.61 to 0.91) and largely used in clinical context and different research projects.58–60 The SOFAS will be administered at T2 to compare eventual improvements by the patient according to the informal caregiver and explore differences in informal caregivers’ outcomes.
Sociodemographic data will be collected at T0: sex, age, education level, professional activity, the nature of their relationship with the patient, whether they live with the patient, the number of close contacts and previous requests for help. Information about the patient will complete the sociodemographic data: the patient’s sex, age, diagnosis according to the caregivers and its duration. No medical data about the patient will be collected which limits the medical diagnosis specification. However, analyses by diagnostic group according to the informal caregiver and the SOFAS level will be done in order to explore differences between groups.
The Satisfaction Scale concerning the Ensemble programme was developed and used in the pilot study.25 This scale will be used only in the post-test evaluation of the intervention group to show the participants’ satisfaction.
The aim of the qualitative part of this project is to conduct a qualitative open and exploratory study. Qualitative data will be collected through semidirective interviews. They will aim to provide significant information regarding participant experiences in the programme (capacities to manage painful emotions and difficulties worked on during the programme and to have and increase awareness of the informal caregiver’s role). Participants will be able to express their views about both advantages and disadvantages of the intervention, and the impacts in the quality of life.
Semidirective interviews will be conducted at the end of the study with 20 selected participants to explore their experiences participating in the Ensemble programme. These participants will be selected at the end of the intervention in the intervention arm. Two groups of participants will be included in this phase: those who have benefited greatly from the programme (G1; n=10) and those who have benefited less (G2; n=10). At the end of the quantitative part for all participants, the 80 subjects will be separated in two groups: those who have a better score and those who have a poorer score in the main outcome (BSI score) in T1 compare to T0. Then for each group, 10 participants will randomly be selected and be contacted for participating in the qualitative study.
This stratification of the sample will allow us to better understand the added value of the Ensemble programme and to identify areas for improvement. The process for this step occurs in two phases: (1) the participant receives information at the time of recruitment and agrees to participate (not only in the project itself but also to the semi-directive interview) and (2) the research team contacts the participants who have consented. Detailed information and conditions will then be given. The participants will have time to read the conditions and think about their participation in this research step. At the time of the interview, before starting the interview and its audio recording, a few minutes will be dedicated to potential questions about the information and consent form or other interrogations. Qualitative data collection will thus constitute both an autonomous inquiry and an opportunity to enrich data obtained through standardised questionnaires.61 Participants will be able to express their views about both advantages and disadvantages of the intervention, and the impacts in the quality of life. In order to ensure that the participant feels free in sharing her/his experiences and challenges, a researcher not involved in the project realisation will conduct these qualitative interviews.
Finally, all standardised questionnaires will be checked at the end of each assessment meeting for the presence of missing data and to reach agreement about how to complete these missing data.
Table 4 presents the plan to retain participants and the completed list of the collected data.
Primary analyses will be conducted on an intent-to-treat basis. To ensure the statistical analyses, a researcher responsible for the analysis will be involved. He/she will double control the final quantitative data before analyses and check the different tests. The following analyses are planned: between-group differences in pretest and post-test values will be examined using an ANCOVA for each outcome variable for the quantitative data. Differences between pretest and post-test scores, as well as between pretest and follow-up scores, will be treated as dependent variables; treatment conditions will be treated as a fixed factor, and pretreatment scores will be treated as covariates. Between-subjects Cohen’s d effect sizes will be calculated at post-test and follow-up. For within subjects, Cohen’s d will be calculated between the pretest and post-test and between the pretest and follow-up, correcting for dependence among means.
The content analysis of the qualitative data will focus on informal caregivers’ experiences in general, as well as their capacity to manage situations. The aim of this analysis is to provide us with a participant’s comprehensive insight into the types of experiences (positive or negative) during the programme, their different capacities and unmet needs. The interview guide (table 5) permits to better show all elements that will be explored during the qualitative study. A content analysis will be provided for each part of the follow-up questions.
Data will be accessible to the investigators and the research assistants during the project. The REDCap platform will control this accessibility. Relevant data will be accessible by a login password to only staff members of this project depending on their responsibilities. For example, an assistant scientific researcher involved in the randomisation phase will only access these data. The data set will be controlled by investigators and transferred to 25 SPSS software before the final analyses. The investigators using the REDCap platform will ensure the traceability of the data and present all the aspects to the audit trial member.
A person external to the project and the institution will audit the data and the project process once a year. She/he will perform the following functions:
Consent checks (100%).
Verification of raw data (first participant all data; for the other participants several randomly selected data).
Verification of Case Report Form (CRF)completeness and consistency: data consistency, data reconciliation, data cleaning, generation of subsequent queries, data derivation, data set formatting prior to statistical analysis, table shells, depersonalisation and anonymisation.
Ethics and dissemination
The research protocol received full authorisation from the Human Research Ethics Committee of the Vaud State, Switzerland. Participants will be informed about the study and their rights and sign a written informed consent form (see online supplementary file: Information et consent_Ensemble). All data will be archived for 10 years after study termination or premature termination of the study. The data pertaining to the hypothesis will be mostly published in open access journals. After priority publications, metadata following Findability, Accessibility, Interoperability and Reuse (FAIR) recommendations will be accessible on the FORSbase platform to allow other researchers to access these data, to proceed with other secondary analyses and to enrich research. This trusted platform offers the possibility of archiving and ensuring the long-term visibility and preservation of the data. Access to the data files will be granted only to researchers external to the project who meet the criteria required by FORSbase.
Adverse event management
Informal caregivers could present painful emotions and could need care for their own health conditions at the beginning of the project and during it. Ethical recommendations allow for those experiencing such adverse events to be enrolled, as they present significant symptoms that are not immediately life-threatening.62 The principal investigators will be informed within 24 hours and will assess the severity of the event as mild, moderate or severe. Mild complications are tolerable, moderate complications interfere with daily activities, and severe complications render daily activities impossible. If a severe adverse event occurs according to Art. 63,62 the research project will be interrupted and the ethics committee will be notified about the circumstances within 15 days according to Human Research Ordinance (HRO) Art. 212.62 Only one severe adverse event not related to the research project occurred during the pilot study. The participant decided merely to stop the project to have time for individual care related to advanced cancer. The informed consent materials and information sheets given to participants are available in French and English through the following website: https://www.seretablir.net/ensemble/
We thank Charles Bonsack and Claude Leclerc for their valuable value in the development of the intervention. We thank Engelhorn for a donation in the first step of the programme development. We also thank members of ÎLOT (The association of informal caregivers for mental disorders, in Vaud state, Switzerland).
Contributors SR and JF designed the study and are grant holders. DW, SM and CC-T collected the data and provided the intervention. SR and JF developed the intervention. SR and SM delivered the study material (eg, the recruitment process, programme figures and web information). SR provided training support for the intervention and data collection during the study. SR led the study but was replaced by JF during maternity leave. PG, JF and SR developed the statistical plan and provided statistical support for the study. SR and SM wrote the first version of the paper. All authors contributed to a critical review and approve the final paper.
Funding Swiss National Science Foundation, grant number 10001C_185422. La Source, School of Nursing, HES-SO University of Applied Sciences and Arts Western Switzerland.The project manager (SR) will be involved in the analysis and interpretation of data, writing of the report and the decision to submit the report for publication. La Source is the only coordinated centre and serves all recruited participants, even those from other French-speaking areas of Switzerland. Lead investigators, SR and JF, will review the process of the study if necessary. SR, as the principal investigator, is responsible for ethical considerations (providing an annual risk report to the ethics committee, providing information on serious adverse events, and announcing any change in the protocol if necessary) and for the study procedures (management of the team and responsible for the data file and budget administration). Noémie Laverne, who was not involved in the execution of the project, is responsible for randomisation even for participants who were randomly by computer, as the computer system requires oversight.The data manager Anne-Laure Kauffman maintains the trial IT system using the REDCap platform and will audit all procedures of the study once a year.
Competing interests None declared.
Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.