Subjective and Objective Methods of Assessing Walking Limitation Due to Claudication
NCT ID: NCT01484509
Last Updated: 2012-05-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
37 participants
OBSERVATIONAL
2011-06-30
2012-05-31
Brief Summary
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The investigators hypothesise that the investigators simple questionnaire will be valid and reliable.
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Detailed Description
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The investigators have developed a simple, 4-item questionnaire, called the Estimation of Ambulation Capacity by History Questionnaire (EACH-Q), for estimating walking capacity in patients with symptomatic PAD (vascular-type claudication). The EACH-Q estimates the maximal duration that can be achieved (8 possibilities ranging impossible to 3 hours or more) at 4 different displacement speeds (from slow walking to running). Scores can be obtained easily by multiplying the rank of each possible answer (impossible being zero) by a speed factor. We recently validated the EACH-Q against constant-load treadmill-walking-test performance in patients suffering from vascular-type claudication. However, further research is needed to assess the validity of the EACH-Q against other objective tests of walking capacity (e.g. incremental treadmill-walking test, 6-min walk test), and to assess its reproducibility.
Hence, the aims of this study are: (i) to assess the validity of the EACH-Q against objective measures of walking capacity obtained from the Gardner-Skinner incremental treadmill-walking test and the 6-min walk test, and; (ii) to assess the inter-day reproducibility of the EACH-Q. The results will be compared against those obtained from the WIQ, and the participant cohort will be patients suffering from vascular-type claudication.
Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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Intermittent claudication
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* presence of leg artery disease with exertional leg symptoms (claudication)
* age 18-90 years
Exclusion Criteria
* medical conditions that make exercise testing unsafe (e.g. unstable angina)
* comorbidities that limit walking performance to a greater extent than claudication symptoms
* unable to complete the tests involved in the study
18 Years
90 Years
ALL
No
Sponsors
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Sheffield Hallam University
OTHER
University Hospital, Angers
OTHER_GOV
Imperial College London
OTHER
Sheffield Teaching Hospitals NHS Foundation Trust
OTHER
Responsible Party
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Principal Investigators
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Garry A Tew, PhD
Role: PRINCIPAL_INVESTIGATOR
Sheffield Hallam University
Pierre Abraham, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
University Hospital of Angers, France
Shah Nawaz, MD
Role: PRINCIPAL_INVESTIGATOR
Sheffield Teaching Hospitals NHS Foundation Trust
Locations
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Sheffield Hallam University
Sheffield, South Yorkshire, United Kingdom
Sheffield Vascular Institute
Sheffield, South Yorkshire, United Kingdom
Countries
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References
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Tew G, Copeland R, Le Faucheur A, Gernigon M, Nawaz S, Abraham P. Feasibility and validity of self-reported walking capacity in patients with intermittent claudication. J Vasc Surg. 2013 May;57(5):1227-34. doi: 10.1016/j.jvs.2012.02.073. Epub 2013 Feb 4.
Other Identifiers
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STH16036
Identifier Type: -
Identifier Source: org_study_id
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