Walking Impairment Questionnaire in PAD (WELCH)

The recruitment status of this study is unknown because the information has not been verified recently.

Verified June 2010 by University Hospital, Angers.
Recruitment status was Recruiting

Sponsor:

Information provided by:

University Hospital, Angers

ClinicalTrials.gov Identifier:

NCT01114178

First received: April 28, 2010

Last updated: June 24, 2010

Last verified: June 2010

History of Changes

Purpose

Purpose is to test and validate a new questionnaire (the WELCH questionnaire) to estimate walking capacity in patients with claudication

Condition	Intervention
Peripheral Artery Disease	Other: questionnaire

Study Type:	Observational
Study Design:	Observational Model: Cohort Time Perspective: Prospective
Official Title:	Estimation de la capacité Fonctionnelle à la Marche Par Questionnaire Clinique Chez Des Patients adressés Pour un Test de Marche Sur Tapis Roulant

Resource links provided by NLM:

MedlinePlus related topics: Peripheral Arterial Disease

U.S. FDA Resources

Further study details as provided by University Hospital, Angers:

Primary Outcome Measures:

scoring of the WELCH questionnaire [ Time Frame: 1 day ] [ Designated as safety issue: No ]
predetermined score for the WELCH questionnaire answers (4 questions)

Estimated Enrollment:	400
Study Start Date:	November 2009
Estimated Study Completion Date:	November 2011
Estimated Primary Completion Date:	November 2011 (Final data collection date for primary outcome measure)

Groups/Cohorts	Assigned Interventions
claudicants patients referred for a treadmill test	Other: questionnaire self completed questionnaire supervised by a technician

Detailed Description:

Questionnaires (WELCH and WIQ) submitted to patients referred for treadmill walking test Comparison of sore to MWD on treadmill. Comparison with WIQ will be performed

Eligibility

Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No
Sampling Method:	Non-Probability Sample

Study Population

patients referred for treadmill testing

Criteria

Inclusion Criteria:

informed consent signed, french language fluent patients

Exclusion Criteria:

rejection of the questionnaire

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT01114178

Contacts

Contact: Pierre Abraham, MD PhD	+33 241353637	piabraham@chu-angers.fr
Contact: Denise Jolivot, MD		dejolivot@chu-angers.fr

Locations

France
University Hospital	Recruiting
Angers, France
Contact: abraham piabraham@chu-angers.fr
Principal Investigator: abraham

Sponsors and Collaborators

University Hospital, Angers

Investigators

Study Chair:

denise Jolivot, MD

University Hospital

More Information

No publications provided by University Hospital, Angers

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Mahe G, Ouedraogo N, Marchand J, Vielle B, Picquet J, Leftheriotis G, Abraham P. Self-reported estimation of usual walking speed improves the performance of questionnaires estimating walking capacity in patients with vascular-type claudication. J Vasc Surg. 2011 Nov;54(5):1360-5.

Mahe G, Ouedraogo N, Vasseur M, Faligant C, Saidi K, Leftheriotis G, Abraham P. Limitations of self-reported estimates of functional capacity using the Walking Impairment Questionnaire. Eur J Vasc Endovasc Surg. 2011 Jan;41(1):104-9. Epub 2010 Nov 30.

Responsible Party:	abraham, University hospital
ClinicalTrials.gov Identifier:	NCT01114178 History of Changes
Other Study ID Numbers:	PL 2009/14
Study First Received:	April 28, 2010
Last Updated:	June 24, 2010
Health Authority:	France: Ministry of Health

Keywords provided by University Hospital, Angers:

questionnaire
peripheral artery disease
exercise

Additional relevant MeSH terms:

Peripheral Arterial Disease
Atherosclerosis
Arteriosclerosis
Arterial Occlusive Diseases

Vascular Diseases
Cardiovascular Diseases
Peripheral Vascular Diseases

ClinicalTrials.gov processed this record on May 19, 2013

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