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Understanding How Peer Support Helps in Mental Health Care (PAIR-PROS)

1 de octubre de 2026 actualizado por: University of Bordeaux

Psychological Processes Associated With Professional Peer Support in Mental Health Amoug Psychiatric Service Users

The goal of this observational study is to better understand the psychological processes associated with professional peer support among adults using psychiatric services. The main questions it aims to answer are:

Do users perceive greater similarity and less dehumanization with peer workers compared with other mental health professionals? Are perceived similarity and dehumanization associated with users' empowerment and hope? Researchers will compare participants' perceptions of a peer worker and another mental health professional who have supported them during the past 12 months.

Participants will complete an online questionnaire about their experiences with both professionals, including measures of perceived similarity, therapeutic alliance, perceived dehumanization, empowerment, and hope. The order in which participants answer questions about the peer worker and the other mental health professional will be randomized.

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Tipo de estudio

De observación

Inscripción (Estimado)

160

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

      • Bordeaux, Francia
        • Université de Bordeaux - Laboratoire de psychologie UR4139 - Faculté de Psychologie
        • Contacto:
        • Sub-Investigador:
          • Adrien SEGELA
        • Sub-Investigador:
          • Felix SIMON

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 65 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

Adults experiencing or having experienced mental health difficulties who have received support from both a professional peer worker and another mental health professional within the past 12 months. Participants will be recruited in France through mental health services, professional and peer-support networks, associations, and online communication channels

Descripción

Inclusion Criteria:

  • Experiencing or having experienced mental health difficulties. Having received support from mental health professionals within the past 12 months.
  • Having received support from a professional peer worker within the past 12 months.
  • Being able to identify a specific mental health professional who provided support during the past 12 months.
  • Being able to identify a specific professional peer worker who provided support during the past 12 months.

Exclusion Criteria :

  • Not meeting inclusion criteria
  • Not understanding French
  • Have expressed their objection to taking part by not ticking the box stating "I have read the information above and declare that I do not object to the use of my data for the purposes of this research"

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Modelos observacionales: OTHER
  • Perspectivas temporales: CROSS_SECTIONAL

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Mental health service users

Adults experiencing mental health difficulties who are currently receiving or have received support from both a professional peer worker and another mental health professional within the past 12 months.

No active intervention is administered as part of this observational study. Participants will complete an online questionnaire about their experiences with a professional peer worker and another mental health professional who have supported them within the past 12 months. For each professional, participants will complete measures of perceived similarity and perceived dehumanization, therapeutic alliance as well as measures of empowerment and hope. The order of the two assessment conditions will be randomized.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
French Empowerment scale (Designes et al. 2025)
Periodo de tiempo: At enrollment, referring to support received within the past 12 months.

French Empowerment Scale (ES), 18 items, from 1 (strongly agree) to 4 (strongly disagree).

Min = 18 Max = 72. Higher score on the scale indicates a high level of empowerment.

At enrollment, referring to support received within the past 12 months.

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
French version of the Adult dispositional hope scale (Gana et al. 2012)
Periodo de tiempo: At enrollment, referring to support received within the past 12 months

French version of the adult dispositional hope scale (ADHS), 12 items, from 1 (always false) to 8 (always true).

Min = 8 Max = 64. Higher score on the scale indicates a high level of dispositional hope.

At enrollment, referring to support received within the past 12 months
Perceived similarity
Periodo de tiempo: At enrollment, referring to support received within the past 12 months.

Created and pre tested measure, 1 item, from 1 (very different) to 6 (very similar).

Min=1 Max = 6. Higher score indicates a high level of similarity.

At enrollment, referring to support received within the past 12 months.
The experience of dehumanization measurement (Gollossenko et al. 2023)
Periodo de tiempo: At enrollment, referring to support received within the past 12 months

The experience of dehumanization measurement (EDHM), adapted to french following best-practice guidelines, 10 items, from 1 (strongly disagree) to 5 (strongly agree).

Min = 10 Max = 50. Higher score on the scale indicates a high level of perceived dehumanization

At enrollment, referring to support received within the past 12 months
Working alliance inventory short form (Corbière et al. 2006)
Periodo de tiempo: At enrollment, referring to support received within the past 12 months

Working Alliance Inventory Short Form (WAISF), 12 items, from 1(never) to 7 (always).

Min = 12 Max = 84. Higher score on the scale indicates a high level of therapeutic alliance

At enrollment, referring to support received within the past 12 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Antoinette PROUTEAU, PhD, Université de Bordeaux - Laboratoire de psychologie UR4139 - Faculté de Psychologie

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de septiembre de 2027

Finalización del estudio (Estimado)

1 de septiembre de 2027

Fechas de registro del estudio

Enviado por primera vez

24 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

24 de septiembre de 2026

Publicado por primera vez (Actual)

30 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

6 de octubre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

1 de octubre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 26.02270.000423
  • 2026-A01111-50 (Otro número de subvención/financiamiento: ANSM)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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