Skip to main content
Clinical Trials/NCT05140577
NCT05140577
Enrolling By Invitation
Not Applicable

Reliability and Validity of the Measurement Procedure for the Evaluation of Hip Abductors Strength in Unipodal Standing Position

HES-SO Valais-Wallis1 site in 1 country72 target enrollmentNovember 1, 2021
ConditionsHealthy People

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy People
Sponsor
HES-SO Valais-Wallis
Enrollment
72
Locations
1
Primary Endpoint
Inter-tester correlation
Status
Enrolling By Invitation
Last Updated
2 years ago

Overview

Brief Summary

The aim is to evaluate the intra- and inter-tester reliability, construct validity and feasibility of a new functional measurement procedure in a closed chain position on one leg. For this purpose, we will test the maximal voluntary isometric force, as well as the muscular contraction speed of the hip abductor muscles.

Detailed Description

Within this Master thesis project, we will investigate intra- and inter-tester reliability, as well as construct validity of a measurement procedure to assess hip abductor strength in a closed-chain position. Additionally, we aim to investigate some aspects of feasibility using a questionnaire about the measurement procedure and by evaluating if the test can be completing in a suitable timeframe for practical use. To investigate intra- and inter-tester reliability, as well as construct validity, we will analyze and compare the maximal voluntary isometric strength (MVIS) and the rate of force generated (RFG) of the three groups of healthy participant (group 1: 18-30 years old; group 2: 31-65 years old; group 3: 65+ years old).

Registry
clinicaltrials.gov
Start Date
November 1, 2021
End Date
June 5, 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Persons over 18 years old, good understanding of French, German, English or Italian, with the capacity of discernment regarding their own participation in the study

Exclusion Criteria

  • Persons with cognitive impairment or who are unable to take their own decisions about participation in the study, or who have undergone surgery on the lower limb or lumbopelvic area during the last 6 months that could contradict or influence the strength tests, will be excluded from the study

Outcomes

Primary Outcomes

Inter-tester correlation

Time Frame: 1 March, 2022

Strength of correlation the measured values

Intra-tester Correlation

Time Frame: 1 March, 2022

Strength of correlation the measured values

Construct validity

Time Frame: 1 March, 2022

Difference between groups by comparing values

Secondary Outcomes

  • Feasibility of the measurement procedure(1 March, 2022)

Study Sites (1)

Loading locations...

Similar Trials