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Programa Ensemble de Intervenção Precoce para Cuidadores Informais de Pacientes Psiquiátricos (Ensemble)

24 de setembro de 2026 atualizado por: Shyhrete Rexhaj, Institut et Haute Ecole de la Santé la Source

Programa Ensemble de intervenção precoce para cuidadores informais de pacientes psiquiátricos: um ensaio controlado randomizado

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.

Visão geral do estudo

Status

Concluído

Condições

Descrição detalhada

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.

Tipo de estudo

Intervencional

Inscrição (Real)

160

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Canton of Vaud
      • Lausanne, Canton of Vaud, Suíça, 1004
        • La Source, School of Nursing Sciences, HES-SO University of Applied Sciences Western Switzerland, Lausanne.

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos a 90 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Cuidados de suporte
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Ensemble + SAU (Support as usual)

The five-session Ensemble program provided to informal caregivers targeted support + SAU

Ensemble is a individualized programme to address informal caregiver's specific unmet needs, emotions and social resources, in order to offer a targeted support in five sessions.

Outros nomes:
  • Conjunto

Informal caregivers have often to manage the situation in usual different ways. Support as usual (SAU) alone consists of an informal support by patient's clinical team. Specific psychoeducational programs depending on patient's illnes (like "Profamille" for schizophrenia) or peer-support depending to the voluntary work of families' associations. Some general professional services focused on informal caregivers or relatives in order to inform and orient them if they are avaible in the study area. No attempts have been made to standardize this treatement as SAU depend to informal caregiver's need and knowledge of the health system, also her/his capacity or possibility to be in contact with patient's clinical team.

Outros nomes:
  • Suporte como de costume
Comparador Ativo: SAU (Support as usual)

SAU alone which was chosen as a control condition.

Informal caregivers have often to manage the situation in usual different ways. Support as usual (SAU) alone consists of an informal support by patient's clinical team. Specific psychoeducational programs depending on patient's illnes (like "Profamille" for schizophrenia) or peer-support depending to the voluntary work of families' associations. Some general professional services focused on informal caregivers or relatives in order to inform and orient them if they are avaible in the study area. No attempts have been made to standardize this treatement as SAU depend to informal caregiver's need and knowledge of the health system, also her/his capacity or possibility to be in contact with patient's clinical team.

Outros nomes:
  • Suporte como de costume

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
General Distress by Global Severity Index
Prazo: Baseline, T1 at 2 months, and T2 at 4 months

The Brief Symptom Inventory (BSI) invlude normative data to detect clinical symptoms as indicators of emotional distress, with 53 items on a 5-point Likert-type scale (0-4), ranging from "not at all"=0 to "extremely=4." The items measure physical and psychological symptoms occurring in the preceding 7-day period. It includes three global indices: Global Severity Index (GSI, indicating the global distress level), Positive Symptom Total (PST, indicating the number of symptoms an individual reports) and Positive Symptom Distress Index (PSDI, indicating the average distress level).The Global Severity Index (GSI) is a composite score to measure global distress Min = 0; Max=212: Range 0-3.83, a higher score reprensent a severer global distress level. The interpretation

Baseline, T1 at 2 months, and T2 at 4 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Optimism Level
Prazo: Baseline, T1 at 2 months, and T2 at 4 months

Assessement of optimism level (LOT-R scale). The Life Orientation Test - Revised (LOT-R) measures an individual's optimism regarding a given situation. This scale includes 10 items; three items measure optimism, three other measure pessimism, and four of the 10 items function as fillers. Items are answered by a Likert-type of scale which varies from 0 (strongly disagree) to 4 (strongly agree). LOT-R score can range from 0 to 24, Min=0, Max=40; 0-13 Low Optimism (High Pessimism); 14-18 Moderate Optimism; 19-24 High Optimism (Low Pessimism). Higher values represent better outcome.

Baseline, T1 at 2 months, and T2 at 4 months
Quality of Live - Mental Dimension
Prazo: Baseline, T1 at 2 months, and T2 at 4 months

36-item Medical Outcome Study Short-Form Health Survey (SF-36) measures health indicators related to the quality of life by 36 items, used in clinical and general population settings to evaluated 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. Higher score defines a more favorable health state. Each item is scored on a 0 to 100 range, 0 being the lowest and 100 being the highest possible scores.Two global scores, i) A Physical Component Score (PCS) and ii) the Mental Component Score (MCS) obtained by grouping dimensions to have global variables (min=0; max =400). MCS is the addition of the mean scores on the emotional well-being, social functioning,vitality and emotional limitation subscales. Lower MCS scores potentially indicate presence of psychological risk.

Baseline, T1 at 2 months, and T2 at 4 months
Burden Level
Prazo: Baseline, T1 at 2 months, and T2 at 4 months

Assessment of the informal caregiver's burden level by the Zarit Burden Interview. This 22-item scale assesses the subjective burden (emotional, physical and financial) for an informal caregiver of an individual with loss of autonomy. The score is obtained by the addition of the 22 items. Scores range between 0 and 88, 61-88 is considered as a high burden, 41-60 is a moderate to high burden, 21-40 is a light to moderate burden and 0-20 is considered as no subjective burden.

Baseline, T1 at 2 months, and T2 at 4 months
Patient's Social an Occupational Functioning
Prazo: Baseline and T2 at 4 months

Social and Occupational Functioning Assessment Scale (SOFAS) is a scale from 0 to 100 demonstrating the patient's social functioning. In this study, this score will be measured according to the informal caregiver's representation. It is used in psychiatry to evaluate how well a patient is functioning in daily life, work, and social relationships.High scores (≥70) indicate good to excellent functioning; Moderate scores (50-69) suggest some difficulties but still some level of independence; Low scores (<50) indicate serious impairments in daily life, often requiring intervention

Baseline and T2 at 4 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Shyhrete Rexhaj, Institut et Haute école de la Santé, La Source

Publicações e links úteis

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Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de setembro de 2019

Conclusão Primária (Real)

1 de janeiro de 2021

Conclusão do estudo (Real)

30 de abril de 2023

Datas de inscrição no estudo

Enviado pela primeira vez

12 de julho de 2019

Enviado pela primeira vez que atendeu aos critérios de CQ

15 de julho de 2019

Primeira postagem (Real)

16 de julho de 2019

Atualizações de registro de estudo

Última Atualização Postada (Real)

25 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

24 de setembro de 2026

Última verificação

1 de maio de 2025

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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