Traduction and Validation of the Central Sentitization Inventory Into French

October 17, 2014 updated by: Cliniques universitaires Saint-Luc- Université Catholique de Louvain
The study will include a translation of the Central Sensisization Inventory into French and a cultural validation of the French version of the questionnaire (Reliability, discrimination and comparison with other questionnaires).

Study Overview

Status

Unknown

Conditions

Study Type

Observational

Enrollment (Anticipated)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Belgium
      • Bruxelles, Belgium, 1200
        • Cliniques Universitaires Saint-luc

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

3 groups:

Fibromyalgia Patients (group 1) Acute or subacute Ankle Sprain (Group 2) Healthy Volunteers (Group 3)

Description

Inclusion Criteria:

  • Clinical Diagnosis of Fibromyalgia (Group 1)
  • Clinical Diagnosis of a Acute of Subacute Ankle Spain (Group 2)
  • Healthy Volunteer (Group 3)

Exclusion Criteria:

  • Having any chronic pain (group 1 and group 2)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Fibromyalgia Patients

The central Sensitization questionnaire will be filled in by each patients included.

After One week, patients will filled it the questionnaire again to study the reliability.
Ankle sprain Patients
The central Sensitization questionnaire will be filled in by each patients included.
Healthy Volunteers

The central Sensitization questionnaire will be filled in by each volunteer included.

After One week, volunteers will filled it the questionnaire again to study the reliability.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Reliability of the French version the Central Sensitization Inventory Score
Time Frame: 1 week
1 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2014

Primary Completion (Anticipated)

June 1, 2015

Study Registration Dates

First Submitted

October 17, 2014

First Submitted That Met QC Criteria

October 17, 2014

First Posted (Estimate)

October 21, 2014

Study Record Updates

Last Update Posted (Estimate)

October 21, 2014

Last Update Submitted That Met QC Criteria

October 17, 2014

Last Verified

October 1, 2014

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CSI-French

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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