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Walking Estimated Limitation Calculated by History - Study 2

Estimation de la capacité Fonctionnelle à la Marche Par Questionnaire Clinique Chez Les Patients adressés Pour Bilan artériel Des Membres inférieurs

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01424020
Acronym
WELCH-2
Enrollment
800
Registered
2011-08-26
Start date
2011-09-30
Completion date
2017-11-30
Last updated
2016-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peripheral Artery Disease

Keywords

Questionnaire, peripheral artery disease, execise

Brief summary

The purpose of this study is to test and validate a new questionnaire in order to get a walking estimated limitation calculated by history (WELCH) in patients referred for vascular investigations.

Detailed description

Two questionnaires the WELCH and the walking impairment questionnaire (WIQ) are submitted to patients referred for vascular investigations for suspêcted peripheral arterial disease (PAD). Comparison of score to hemodynamic parameters (first goal) or maximal walking distance (MWD) on treadmill (secondary goal). Scoring of the WIQ is performed according to references. Scoring of the WELCH has been submitted for copyright protection (involves a series of 4 additions a subtraction and a single multiplication)

Interventions

OTHERQuestionnaire

Self completed questionnaire, Supervised by the physician Ankle brachial index (ABI) calculation Maximal walking distance (MWD) on treadmill or over the 6 minutes walking test (when available)

Sponsors

University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* French Native language * 18 years old or older * Signed consent * Covered by the French social care system

Exclusion criteria

* Unable to participate for administrative reasons * Psychiatric troubles * Pain at rest or critical limb ischemia * Unable to walk (ex: wheelchair subjects) Note: previous inclusion in the protocole is note an exclusion criterion for a new participation.

Design outcomes

Primary

MeasureTime frameDescription
Proportion of questionnaires with errors after self completion1 dayAnalysis of first inclusion only in patients that are included multiple times over the study period. Predetermined score for the WELCH questionnaire answers \[(4 items); (4 additions & 1 multiplication)\] and WIQ... estimation of the percentage of errors with 95% confidence interval. Comparison of the two percentages

Secondary

MeasureTime frameDescription
Correlation with ankle brachial index (ABI)1 dayAnalysis of first inclusion only in patients that are included multiple times over the study period. Calculation of questionnaire scores from predetermined methods and analysis of the coefficient of determination and coefficient of correlation to minimal ABI
Correlation with treadmill result1 dayAnalysis of first inclusion only in patients that are included multiple times over the study period.Calculation of questionnaires score from predetermined methods and analysis of the coefficient of determination and coefficient of correlation to maximal walking distance on treadmill, in the subgroup of patients that have a routine treadmill scheduled during the visit.
Facility of the scoring of the questionnaires1 dayProportion of WELCH scores calculated by physician and comparison to the proportion of WIQ score calculated by physicians as a estimation of the facility to calculate the score by mental calculation in routine
Reliability of the questionnaire3 weeksComparison of the scores of the WELCH in the patients that may be seens within 3 weeks of their first inclusion, for any reasons, (e.i. seen first for a doppler and two weeks later for a treadmill test)over the study period. Analysis of the reliability through the coefficient of variation of the score.
sensitivity of the WELCH to changes1 yearComparison of the scores of the WELCH in the patients that may be seens within 1 year from their first inclusion, for any reasons, (e.i. seen follow up of their disease)over the study period. Analysis of the changes of the score to changes of the ABI. Analysis of the changes of the score to changes in maximal walking distance if available.

Countries

France

Contacts

Primary ContactPierre Abraham, MD; PhD
piabraham@chu-angers.fr33 (0) 2 41 35 36 89
Backup ContactJohann Marchand, MD
welch@gernigon.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026