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

1. oktober 2026 opdateret af: 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.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Undersøgelsestype

Observationel

Tilmelding (Anslået)

160

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

      • Bordeaux, Frankrig
        • Université de Bordeaux - Laboratoire de psychologie UR4139 - Faculté de Psychologie
        • Kontakt:
        • Underforsker:
          • Adrien SEGELA
        • Underforsker:
          • Felix SIMON

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

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

Beskrivelse

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"

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Observationsmodeller: OTHER
  • Tidsperspektiver: CROSS_SECTIONAL

Kohorter og interventioner

Gruppe / kohorte
Intervention / Behandling
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.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
French Empowerment scale (Designes et al. 2025)
Tidsramme: 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.

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
French version of the Adult dispositional hope scale (Gana et al. 2012)
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Antoinette PROUTEAU, PhD, Université de Bordeaux - Laboratoire de psychologie UR4139 - Faculté de Psychologie

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. september 2026

Primær færdiggørelse (Anslået)

1. september 2027

Studieafslutning (Anslået)

1. september 2027

Datoer for studieregistrering

Først indsendt

24. september 2026

Først indsendt, der opfyldte QC-kriterier

24. september 2026

Først opslået (Faktiske)

30. september 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

6. oktober 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

1. oktober 2026

Sidst verificeret

1. oktober 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 26.02270.000423
  • 2026-A01111-50 (Andet bevillings-/finansieringsnummer: ANSM)

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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