NCT07667686

Brief Summary

The VAL-RAS-FR study aims to cross-culturally adapt, validate, and develop derived versions of the Recovery Assessment Scale (RAS), an internationally used self-report measure of subjective recovery in mental health. The study will include 260 adult psychiatric patients receiving care at EPSM Metz-Jury in both inpatient and outpatient settings. Participants will complete the French version of the RAS (RAS-FR), the WHOQOL-BREF, and additional self-report questionnaires. A subgroup of participants will complete the RAS-FR again after one month to assess test-retest reliability. The study will also explore existential aspects of recovery through the development of the RAS-FR-EX (Existential Extension) and support the development of a shorter version, the RAS-FR-SF (Short Form), for clinical and research purposes.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
260

participants targeted

Target at P75+ for all trials

Timeline
13mo left

Started Jun 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress14%
Jun 2026Sep 2027

Study Start

First participant enrolled

June 1, 2026

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

June 16, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 25, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2027

Last Updated

June 25, 2026

Status Verified

June 1, 2026

Enrollment Period

7 months

First QC Date

June 16, 2026

Last Update Submit

June 19, 2026

Conditions

Keywords

subjective recoverypsychiatric carepsychometric validationRecovery Assessment Scalepatient-reported outcomemental healthRASmental health recoveryquality of lifeWHOQOL-BREFcross-cultural adaptationrecovery-oriented careexistential recoveryRAS-FRFrench validation

Outcome Measures

Primary Outcomes (1)

  • Recovery Assessment Scale - French Version (RAS-FR): Total Score, Internal Consistency, Factor Structure, and Test-Retest Reliability

    The Recovery Assessment Scale - French Version (RAS-FR) is a 41-item self-report questionnaire assessing subjective recovery in mental health. Total scores range from 41 to 205, with higher scores indicating a higher level of subjective recovery. Psychometric analyses will include internal consistency, dimensional structure, and test-retest reliability.

    Baseline and 1 month

Secondary Outcomes (3)

  • Correlation between Recovery Assessment Scale - French Version (RAS-FR) and WHOQOL-BREF (World Health Organization Quality of Life - Brief Version) scores

    Baseline

  • Existential dimension of recovery (RAS-FR-EX) composite score

    Baseline

  • Development of a short-form Recovery Assessment Scale - French Version (RAS-FR-SF)

    Baseline

Study Arms (1)

Adult psychiatric patients

Adult psychiatric patients receiving care at EPSM Metz-Jury (inpatient units, day hospital, community mental health centers \[CMP\], and intensive home-based psychiatric care services \[EPSIAD\]) who are able to complete self-report questionnaires in French.

Other: Self-report questionnaires

Interventions

Participants complete self-report questionnaires including the French version of the Recovery Assessment Scale (RAS-FR), the WHOQOL-BREF, and complementary questionnaires related to subjective recovery. The study also includes the exploratory assessment of six additional existential items. A subgroup of 50 participants will complete the RAS-FR again after one month to assess test-retest reliability. No therapeutic intervention, modification of usual care, invasive procedure, or additional medical examination is involved.

Adult psychiatric patients

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult psychiatric patients receiving care at EPSM Metz-Jury in inpatient units, day hospital settings, community mental health centers (CMP), or through intensive home-based psychiatric care services (EPSIAD). Participants are French-speaking adults able to complete self-report questionnaires independently or with assistance if needed. Patients under legal protection measures may participate in accordance with applicable regulations.

You may qualify if:

  • Adult patient (18 years or older)
  • Receiving psychiatric care at EPSM Metz-Jury (inpatient unit, day hospital, community mental health center \[CMP\], or intensive home-based psychiatric care service \[EPSIAD\]/post-EPSIAD follow-up)
  • Able to understand French
  • Able to complete a self-report questionnaire independently or with assistance if needed
  • Patients under legal protection measures (guardianship or curatorship) may participate with the agreement of their legal representative, when applicable

You may not qualify if:

  • Major cognitive impairment
  • Severe clinical condition preventing questionnaire completion or understanding of French
  • Refusal to participate
  • Prisoner or person deprived of liberty by judicial or administrative decision

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

EPSM Metz-Jury

Jury, Moselle, 57245, France

Location

MeSH Terms

Conditions

Psychological Well-BeingMental Disorders

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior

Study Officials

  • Audrey WILLIG, Psychologist

    Clinical Research Unit (URC), EPSM Metz-Jury

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Audrey WILLIG, Psychologist

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 16, 2026

First Posted

June 25, 2026

Study Start

June 1, 2026

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

September 1, 2027

Last Updated

June 25, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) will not be made publicly available. Access to study data may be considered on a case-by-case basis upon request to the sponsor, subject to regulatory requirements, confidentiality obligations, and GDPR compliance.

Locations