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PERMAPROFILER2: Psychometric Validation of a French-language Version of the PERMA-Profiler: Tools for Assessing Multidimensional Subjective Well-being

Sponsor
Centre Hospitalier Universitaire de Nīmes (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05930353
Collaborator
(none)
400
Enrollment
1
Location
7
Anticipated Duration (Months)
57.2
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The main objective of this study is to carry out the psychometric validation of the PERMA-Profiler in a population representative of the general French population and in comparison with the reference questionnaire The PERMA-Profiler.

Condition or Disease Intervention/Treatment Phase
  • Other: COHORT

Study Design

Study Type:
Observational
Anticipated Enrollment :
400 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Psychometric Validation of a French-language Version of the PERMA-Profiler: Tools for Assessing Multidimensional Subjective Well-being
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Apr 1, 2024

Outcome Measures

Primary Outcome Measures

  1. PERMA PROFILER French Version: diagnostic properties [DAY 0]

    sensitivity, specificity

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

  • Adult (≥18 years).

  • Person able to read and understand French

  • Person willing to participate in this study

Exclusion Criteria:

  • The person does not understand the French language

  • Person has a history of traumatic brain injury

  • The person refuses to participate in the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Chu de Nimes Nimes France 30029

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nīmes

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nīmes
ClinicalTrials.gov Identifier:
NCT05930353
Other Study ID Numbers:
  • LOCAL/2023/JJ-01
First Posted:
Jul 5, 2023
Last Update Posted:
Jul 5, 2023
Last Verified:
Jun 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Mental Disorders
Problem Behavior

Study Results

No Results Posted as of Jul 5, 2023