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COMPLETED
NCT04646343

Cross-cultural Adaptation and Validation of the CISS and the PWES Questionnaire in Patients With Hand Pathologies.

Sponsor: Clinique Romande de Readaptation

View on ClinicalTrials.gov

Summary

The primary objective of the study is to do translation, cross-cultural adaptation and validation of the CISS and PWES questionnaire in French. No available translation exist in French. In the first part of the study, the investigators will use clinical guidelines for translation and cross-cultural adaptation of questionnaire (Beaton and al).The content validity will be evaluated also in this first step. In the second part of the study the French version of CISS and PWES (F-CISS and F-PWES) will be validated. Different psychometric properties (internal consistency, test retest reliability, construct validity, floor and ceiling effects) will be study. The investigators use the recommendation of COSMIN (COnsensus- based Standards for the selection of health Measurement INstruments) group.

Official title: Cross-cultural Adaptation and Validation of the "Cold Intolerance Symptom Severity Questionnaire" (CISS) and the "Potential Work Exposure Scale" (PWES) in Patients With Hand Pathologies.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2020-12-01

Completion Date

2026-09-25

Last Updated

2026-09-30

Healthy Volunteers

No

Interventions

OTHER

administration of F-CISS and F-PWES pre version

the CISS questionnaire is a 6 items questionnaire, the PWES is a 3 items questionnaire. Only 10 minutes are required to fulfilled the questionnaires.

OTHER

administration of definitive version of F-CISS and F-PWES plus F-DASH, F-HFS and F-SF 36

The administration will required 25 minutes

Locations (1)

Clinique romande de réadaptation

Sion, Valais, Switzerland