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NCT01217684 Clinical Trial

Test-retest Reliability of a Standard Protocol on the Biodex Dynamometer

Validity Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01217684
Other study ID # ML 6404
Secondary ID
Status Completed
Phase N/A
First received October 6, 2010
Last updated June 14, 2012
Start date October 2010
Est. completion date May 2012

Study information
Verified date June 2012
Source Universitaire Ziekenhuizen Leuven
Contact n/a
Is FDA regulated No
Health authority Belgium: Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of the present study is to evaluate test-retest reliability of a standard protocol on the Biodex dynamometer in older adults.

In addition, the test-retest reliability and validity of an experimental measure of knee extension strength will be assessed in older adults.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date May 2012
Est. primary completion date May 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- +65 years old

- able to perform a maximal strength test on a dynamometer

Exclusion Criteria:

- pathologies that prohibit a maximal strength test on a dynamometer

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
Belgium Faculty of Kinesiology and Rehabilitation Sciences Leuven

Sponsors (1)
Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

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