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Clinical Trials/NCT04020497
NCT04020497
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Ensemble Programme an Early Intervention for Informal Caregivers of Psychiatric Patients: a Randomized Controlled Trial

Institut et Haute Ecole de la Santé la Source1 site in 1 country70 target enrollmentSeptember 1, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Psychological Distress
Sponsor
Institut et Haute Ecole de la Santé la Source
Enrollment
70
Locations
1
Primary Endpoint
Psychological state change on the Global Severity Index (GSI)
Last Updated
4 years ago

Overview

Brief Summary

This study focuses on the difficulties of maintaining optimal psychological health and quality of life for caregivers in adult psychiatry while they play an important role in helping patients with severe psychiatric disorders. It evaluates the addition of a 5 session psychological program, named Ensemble. Half of the participants will receive their usual support and Ensemble in combination, while the other half will receive usual support only.

Detailed Description

The recent statistics showed that mental disorders affect one in four people in the world. In this context, informal caregivers are key actors in the health care system through their support. This support can be associated with very high burden and distress. Informal caregivers can experience serious situations with potential negative consequences on their quality of life, their own health and the health of patients. Data recommended to intervene at the onset of disease to improve the impact of an intervention. It seems important also to intervene while the patient is in an acute phase of illness to better support informal caregivers' emotional needs. In addition, providing emotional support for informal caregivers at the beginning of an illness in particular is recommended because this is a critical phase. The experience of painful emotions, such as denial of disease and feelings of being overwhelmed or shocked can have serious consequences on their health and on the patient's recovery. Previous studies identified that informal caregivers need tailored knowledge about the patient's illness, clarification about their roles and responsibilities, better control over their own life and effective collaboration with health professionals. Most of the interventions published in the literature focus on the ill family member and its support but not on the specific needs of the informal caregivers as the core intervention. To reduce the gap between scientific recommendations and actual practice, the investigators developed, tailored and tested a new intervention called Ensemble. Ensemble is a brief individualized intervention designed to promote the well-being of informal caregivers who experience the effects of patients' psychiatric disorders. The five-session Ensemble program provided to informal caregivers targeted support to address their specific unmet needs, emotions and social resources. A professional addressed this programme to the informal caregiver delivered independently of the patient's treatment. Ensemble assesses the needs of informal caregivers and provides a tailored brief support. Results of a pilot study showed that psychological health and optimism of informal caregivers were improved. For these reasons, there is a clear research and clinical need to establish whether Ensemble programme is clinically effective by using a randomized, controlled, and assessor-blind trial. A combination of Ensemble plus support as usual (SAU) will be compared to SAU alone. Informal caregivers of individuals suffering from mental disorders will undergo either intervention for five sessions, during a six weeks average time. Measure will assess participants' current psychological health state and optimism. These different measures will be performed at the time of inclusion, at the end of the intervention, and at two months follow-up. At the end of the program, individual qualitative structured interviews will be performed to assess acceptability of the programme.

Registry
clinicaltrials.gov
Start Date
September 1, 2019
End Date
April 30, 2023
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Institut et Haute Ecole de la Santé la Source
Responsible Party
Principal Investigator
Principal Investigator

Shyhrete Rexhaj

Porfessor associate HES

Institut et Haute Ecole de la Santé la Source

Eligibility Criteria

Inclusion Criteria

  • Being at least 18 years old
  • Living in the French-speaking cantons of Switzerland (commonly referred to as "Romandy")
  • Speaking French
  • Having an adult relative suffering from a psychiatric disorder (with or without an established diagnosis)
  • Having the capacity to agree to participate in the project

Exclusion Criteria

  • Having les than 20 on the Zarit score.

Outcomes

Primary Outcomes

Psychological state change on the Global Severity Index (GSI)

Time Frame: Change from Baseline composite on the GSI score at post-test, and at 2 months follow

Assessment of psychological symptoms and psychological distress (BSI scale). The Brief Symptom Inventory (BSI) includes 53 items organized into 9 primary and clinically relevant symptom dimensions: 1) somatization, 2) obsessive-compulsive, 3) interpersonal sensitivity, 4) depression, 5) anxiety, 6) hostility, 7) phobic anxiety, 8) paranoid ideation and 9) psychoticism. This scale has also three global distress indices: The Global Severity Index (GSI), the Positive Symptom Distress Index (PSDI) and the Positive Symptom Total (PST).

Secondary Outcomes

  • Optimism change on the Life Orientation Test-Revised (LOT-R)(Change from Baseline total score of the LOT-R at post-test, and at 2 months follow)
  • Burden level change on the Zarit Burden Intervieuw (ZBI)(Change from Baseline on the Zarit score at post-test and at 2 months follow)
  • Quality of life change on the Mental Component Score (MCS)(Change from Baseline composite on the MCS score at post-test, and at 2 months follow)
  • Standardized severity of the patient's illness change on the Social an Occupational Functioning Assessment Scale (SOFAS)(Change from Baseline on the SOFAS score at 2 months follow)

Study Sites (1)

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