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

Sponsor
HES-SO Valais-Wallis (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05140577
Collaborator
(none)
72
1
7.1
10.1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Maximal voluntary isometric strengthening

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 Design

Study Type:
Observational
Anticipated Enrollment :
72 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Reliability and Validity of the Measurement Procedure for the Evaluation of Hip Abductors Strength in Unipodal Standing Position
Actual Study Start Date :
Nov 1, 2021
Anticipated Primary Completion Date :
Feb 28, 2022
Anticipated Study Completion Date :
Jun 5, 2022

Arms and Interventions

Arm Intervention/Treatment
18-30 years old

Subjects in this group is aged between 18 ans 30 years old

Other: Maximal voluntary isometric strengthening
The subject is asked to perform a maximum voluntary isometric force work against a wall during 5 seconds

31-65 years old

Subjects in this group is aged between 31 ans 65 years old

Other: Maximal voluntary isometric strengthening
The subject is asked to perform a maximum voluntary isometric force work against a wall during 5 seconds

65+ years old

Subjects in this group is aged over 65 years old

Other: Maximal voluntary isometric strengthening
The subject is asked to perform a maximum voluntary isometric force work against a wall during 5 seconds

Outcome Measures

Primary Outcome Measures

  1. Intra-tester Correlation [1 March, 2022]

    Strength of correlation the measured values

  2. Inter-tester correlation [1 March, 2022]

    Strength of correlation the measured values

  3. Construct validity [1 March, 2022]

    Difference between groups by comparing values

Secondary Outcome Measures

  1. 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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sport Medical Center Ittigen Ittigen Bern Switzerland 3063

Sponsors and Collaborators

  • HES-SO Valais-Wallis

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
HES-SO Valais-Wallis
ClinicalTrials.gov Identifier:
NCT05140577
Other Study ID Numbers:
  • 2021-01829
First Posted:
Dec 1, 2021
Last Update Posted:
Dec 1, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by HES-SO Valais-Wallis

Study Results

No Results Posted as of Dec 1, 2021