Reliability and Validity of the Evaluation of Hip Abductors Strength (RAVEHABDS)

• Conditions: Healthy People

• Registration Number: NCT05140577
• Lead Sponsor: HES-SO Valais-Wallis

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).

Study Timeline

• Study Start: 2021-11-01
• Study First Submitted: 2021-11-22
• Study First Submitted QC: 2021-11-22
• Study First Posted: 2021-12-01
• Status Verified: 2023-09
• Last Update Submitted: 2023-09-25
• Last Update Posted: 2023-09-26
• Primary Completion: 2024-02-28
• Study Completion: 2024-06-05

Recruitment & Eligibility

• Status: ENROLLING_BY_INVITATION
• Sex: All
• Target Recruitment: 72

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Inter-tester correlation	1 March, 2022	Strength of correlation the measured values
Intra-tester Correlation	1 March, 2022	Strength of correlation the measured values
Construct validity	1 March, 2022	Difference between groups by comparing values

Secondary Outcome Measures

Name	Time	Method
Feasibility of the measurement procedure	1 March, 2022	Through the administration of a feasibility questionnaire we investigate the time to perform the test, the understanding of the instructions, the fatigue, the possible pain, or the fear of falling during the test

Trial Locations

Locations (1)

Sport Medical Center Ittigen; 🇨🇭 Ittigen, Bern, Switzerland