- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05236816
Relationship Between Hip Abductor Strength and Ankle Stability (HIAS)
Ankle sprains are one of the most common injuries in sports. The analysis of risk factors is a priority in order to guide rehabilitation and prevention programs. Among risk factors identified in the literature, weakness of the hip abductor muscles represent a factor favoring recurrent ankle sprains. However, only few studies have investigate the link between the strength of the hip abductor muscles and the deficits in stabilization of the ankle joint. Furthermore, these few studies analysed landing task or undisturbed balance task. It would be interesting to further understand the impact and role of hip abductor muscles on ankle stability during specific ankle-destabilizing task.
The main objective of this study is to establish a link between the strength of the hip abductor muscles and the dynamic postural control performance measured by the modified Star Excursion Balance Test (SEBTm). Secondly, it will be necessary to study the kinematic and neuromuscular control characteristics of the ankle during 4 functional tests:
- SEBTm
- Static unipodal balance
- Weight-bearing inversion test
- Weight-bearing eversion test
These tests will be realized with an ankle destabilizing device. The device is a sandal equipped of an articulator under the rear foot which allow movements in inversion and eversion. Furthermore, tests are realized two times, before and immediatly after a fatiguing exercise. The fatiguing exercise consists to implemented local fatigue on hip abductor muscles by repeating abductions.
Study Overview
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Fabrice MICHEL, MD PhD
- Phone Number: +33 3 81 66 82 48
- Email: fmichel@chu-besancon.fr
Study Contact Backup
- Name: Jeanne DURY
- Phone Number: +33 3 81 66 82 48
- Email: jeanne.dury@univ-fcomte.fr
Study Locations
-
-
-
Besançon, France
- Recruiting
- CHU de Besancon
-
Contact:
- Jeanne DURY
- Email: jeanne.dury@univ-fcomte.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Males and females between 18 and 35 years old
- Subject's non-opposition to participate in the study
- Practicing regular physical activity (> 2 hours per week)
- No contraindication to carrying out the protocol
- Affiliation to a French social security scheme or beneficiary of such a scheme
Exclusion Criteria:
- Males or females under 18 or over 35 years
- History of lower limb injuries in the 6 months preceding the protocol
- Diagnosis of chronic ankle instability
- Subject unlikely to cooperate with the study and / or weak cooperation anticipated by the investigator
- Subject's opposition to participating in the study
- Subject without health insurance
- Pregnant woman
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Healthy
Subjects were evaluated before and after a fatiguing exercise of hip abductor muscles that consisted to repeat hip abduction with rate and range of motion until a target decrease of force is attempt
|
Subjects were evaluated before and after a fatiguing exercise of hip abductor muscles that consisted to repeat hip abduction with rate and range of motion until a target decrease of force is attempt
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Surface Electromyography intensity change
Time Frame: 5 minutes before physical exercise
|
Measure of muscles activity if peroneus longus and brevis, tibialis anterior, gluteus medius and gastrocnemuis lateralis using wireless and surface electrodes fixed with strap on the skin of subjects
|
5 minutes before physical exercise
|
|
Surface Electromyography intensity change
Time Frame: 5 minutes after physical exercise
|
Measure of muscles activity if peroneus longus and brevis, tibialis anterior, gluteus medius and gastrocnemuis lateralis using wireless and surface electrodes fixed with strap on the skin of subjects
|
5 minutes after physical exercise
|
|
Frontal inclination of ankle change
Time Frame: 5 minutes before physical exercise
|
Measure of accelerations of ankle joint during tests using inertial measurement unit
|
5 minutes before physical exercise
|
|
Frontal inclination of ankle change
Time Frame: 5 minutes after physical exercise
|
Measure of accelerations of ankle joint during tests using inertial measurement unit
|
5 minutes after physical exercise
|
|
SEBT performances change
Time Frame: 5 minutes before physical exercise
|
Performances (distance in cm) attempted in each direction of the dynamic postural test
|
5 minutes before physical exercise
|
|
SEBT performances change
Time Frame: 5 minutes after physical exercise
|
Performances (distance in cm) attempted in each direction of the dynamic postural test
|
5 minutes after physical exercise
|
|
Hip abductor strength change
Time Frame: 5 minutes before physical exercise
|
Measure of maximal isometric strength with a S-shape force transducer
|
5 minutes before physical exercise
|
|
Hip abductor strength change
Time Frame: 5 minutes after physical exercise
|
Measure of maximal isometric strength with a S-shape force transducer
|
5 minutes after physical exercise
|
|
Angular velocity of ankle change
Time Frame: 5 minutes before physical exercise
|
Measure of angular velocity of ankle joint during tests using inertial measurement unit
|
5 minutes before physical exercise
|
|
Angular velocity of ankle change
Time Frame: 5 minutes after physical exercise
|
Measure of angular velocity of ankle joint during tests using inertial measurement unit
|
5 minutes after physical exercise
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021/655
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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