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Walking Impairment Questionnaire in PAD (WELCH)

This study has been terminated.
(recruitment problem due to administrative process being too long)
Sponsor:
ClinicalTrials.gov Identifier:
NCT01114178
First Posted: May 3, 2010
Last Update Posted: December 19, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
University Hospital, Angers
  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

Further study details as provided by University Hospital, Angers:

Primary Outcome Measures:
  • scoring of the WELCH questionnaire [ Time Frame: 1 day ]
    predetermined score for the WELCH questionnaire answers (4 questions)


Enrollment: 340
Study Start Date: November 2009
Study Completion Date: May 2012
Primary Completion Date: May 2012 (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

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01114178


Locations
France
University Hospital
Angers, France
Sponsors and Collaborators
University Hospital, Angers
Investigators
Study Chair: denise Jolivot, MD University Hospital
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: University Hospital, Angers
ClinicalTrials.gov Identifier: NCT01114178     History of Changes
Other Study ID Numbers: PL 2009/14
First Submitted: April 28, 2010
First Posted: May 3, 2010
Last Update Posted: December 19, 2016
Last Verified: December 2016

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