Validation of the French Version of the Fatigue Score "Brief Fatigue Inventory ( BFI)". (EAMG)

July 11, 2016 updated by: University Hospital, Brest

Validation de la Version française du Score de Fatigue " Brief Fatigue Inventory (BFI)

Fatigue, or asthenia, is an important symptom for the diagnosis and follow-up of patients in routine as well as research oriented clinical practice.

Various questionnaires measuring fatigue have been developed, but few have been validated in french. MFI (Multidimensional Fatigue Inventory) has been validated in french in only one study. BFI (Brief Fatigue Inventory) has been translated but never validated in french language.

The main purpose of this study is to validate psychometrically the french version of BFI.

Study Overview

Status

Unknown

Conditions

Study Type

Observational

Enrollment (Anticipated)

1200

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

  • France
      • Brest, France, 29200
        • Not yet recruiting
        • Cabinet Brest Centre
        • Contact:
          • Pierre Barraine
      • Camaret/mer, France, 29570
        • Recruiting
        • Cabinet Camaret/mer
        • Contact:
          • Jean-François Auffret
      • Ergue Gaberic, France, 29500
        • Not yet recruiting
        • Cabinet Ergue Gaberic
        • Contact:
          • Jean-François Velly
      • Lanmeur, France, 29620
        • Recruiting
        • Cabinet Lamneur
        • Contact:
          • Jean-Yves Le Reste
      • Lanmeur, France, 29620
        • Not yet recruiting
        • Cabinet Lamneur
        • Contact:
          • Emilie Berck-Robert
      • Lanmeur, France, 29620
        • Not yet recruiting
        • Cabinet Lanmeur
        • Contact:
          • Joël Le Roc'h
      • Le Guilvinec, France, 29730
        • Not yet recruiting
        • Cabinet Le Guilvinec
        • Contact:
          • Dominique Le Bail
      • Lesconil, France, 29740
        • Not yet recruiting
        • Cabinet Lesconil
        • Contact:
          • Jean Jérôme Le Coq
      • Penmarch, France, 29760
        • Not yet recruiting
        • Cabinet Penmarch
        • Contact:
          • Jannick Saliou
      • Plouegat Guerrand, France, 29620
        • Not yet recruiting
        • Cabinet Plouegat Guerrand
        • Contact:
          • Daniel Le Floc'h
      • Quimper, France, 29000
        • Not yet recruiting
        • Cabinet Quimper
        • Contact:
          • Nikan Mohtadi
      • Rosporden, France, 29104
        • Recruiting
        • Cabinet Rosporden
        • Contact:
          • Lionel Briand
      • Rosporden, France, 29140
        • Recruiting
        • Cabinet Rosporden
        • Contact:
          • Gérard Larreur

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patient with fatigue symptom consulting a general practitioner

Description

Inclusion Criteria:

  • Consultation for fatigue as symptôme principal ( isolated or asociated with other symptomes).

Exclusion Criteria:

Pregnancy Psychosis. Unable to complete questionnaire Phsyiological fatigue due to effort and reversible rest. Post-traumatic stress disorder -

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

  • Observational Models: Cohort
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
9 points of BFI, each of them between 0 to 10. of BFI
Time Frame: 3 Months
3 Months

Collaborators and Investigators

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

Sponsor

University Hospital, Brest

Investigators

  • Study Director: Chritian Berthou, CHRU de Brest

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

March 1, 2016

Primary Completion (Anticipated)

September 1, 2017

Study Completion (Anticipated)

September 1, 2017

Study Registration Dates

First Submitted

January 4, 2016

First Submitted That Met QC Criteria

January 4, 2016

First Posted (Estimate)

January 5, 2016

Study Record Updates

Last Update Posted (Estimate)

July 12, 2016

Last Update Submitted That Met QC Criteria

July 11, 2016

Last Verified

June 1, 2016

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • EAMG- RB 14.062

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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