Skip to content

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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05140577
Acronym
RAVEHABDS
Enrollment
72
Registered
2021-12-01
Start date
2021-11-01
Completion date
2024-06-05
Last updated
2023-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy People

Keywords

hip abductors strengthening, one-leg standing, maximal voluntary isometric strengthening, rate of force generated, dynamometer, aged category, so surgery

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).

Interventions

OTHERMaximal voluntary isometric strengthening

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

Sponsors

HES-SO Valais-Wallis
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Construct validity1 March, 2022Difference between groups by comparing values
Intra-tester Correlation1 March, 2022Strength of correlation the measured values
Inter-tester correlation1 March, 2022Strength of correlation the measured values

Secondary

MeasureTime frameDescription
Feasibility of the measurement procedure1 March, 2022Through 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

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026