- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06557577
Comparing an Adductor Fatigue Strength Test with Handheld Dynamometry
Evaluation of Hip Muscle Strength: Utility of an Adductor Fatigue Test to Substitute Handheld Dynamometry
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The strength of the adductor muscles in a population of federated athletes will be measured using two tests: First, the maximum strength test, utilizing dynamometry, where the subject will perform a maximal isometric contraction against the resistance provided by the investigator. Subsequently, endurance strength will be measured with the Adductor Fatigue Test (Brazilian Adductor Performance Test), the participant must perform an adductor exercise as many repetitions as possible until exhaution. In order to evaluate a possible correlation between the two tests and thus, by performing one of them, obtain the results of the other variable.
Apart from the strength measurements, democraphic caracteristics will be recorded to assess possible correlations between studied variables.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Asturias
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Oviedo, Asturias, Spain, 33007
- Escuela Profesional de Medicina de la Educación Fisica y el Deporte
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Having an active lifestyle
- Competing at any level in a federated sports discipline.
Exclusion Criteria:
- Not consenting to participate in the research.
- Being unable to understand or write in Spanish.
- Having sustained any type of injury to the inguinal musculature in the past 3 months.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy athletes
Competitive athletes without any groin injury.
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There is no intervention group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximal adductor strength
Time Frame: September to December (2024)
|
Measuring the maximum strength of the adductor musculature, performed manually by a physiotherapist using a dynamometer over a brief working period. To begin the test, the subject should lie in a supine position on a flat surface. Their hip should be positioned at a 0º angle in our case. Ideally, at least three measurements should be taken, including a brief rest (~30 seconds) between each repetition to minimize muscle fatigue. The dynamometer should be placed between both ankles of the patient, with the forearm of the analyzing physiotherapist positioned in the middle as resistance. The patient should exert as much pressure as possible against the dynamometer, which is held by the physiotherapist, and against the physiotherapist's elbow, as if trying to close their legs like scissors, using their adductor muscles and maintaining the contraction for 5 seconds. |
September to December (2024)
|
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Adductor fatigue strength test
Time Frame: September to December (2024)
|
The individual will begin by assuming a side plank position, supported by the elbow, bent, and the forearm (lower arm) on the ground.
The hand of the supporting arm is placed on the waist of the side of the lower limb that is to be evaluated (the highest).
The evaluated limb is supported by a 0.5-meter high bench at the ankle region, while the opposite limb does not touch the ground, remaining in a semi-flexed position.
The subject must control the descent of the pelvis by performing a hip abduction until the pelvis lightly touches the ground, and then return to the initial position by raising the pelvis again.
The score is defined as the maximum number of repetitions completed before reaching muscle failure.
During the test, participants are instructed to keep both legs parallel and to ensure that the knee of the non-evaluated leg remains in a semi-flexed position.
Maintaining the correct alignment of the trunk throughout the exercise is crucial.
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September to December (2024)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight
Time Frame: September to December (2024)
|
Weight (kg)
|
September to December (2024)
|
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Hip and groin outcome score (HAGOS)
Time Frame: September to December (2024)
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A questionnaire will be given to every participant to obtain information on groin pain symptoms in the last week.
Minimum: 0; Maximum: 100.
Higher scores mean better hip and groin health.
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September to December (2024)
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Age
Time Frame: September to December (2024)
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Age (in years)
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September to December (2024)
|
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Sex
Time Frame: September to December (2024)
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Biological sex
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September to December (2024)
|
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Leg length
Time Frame: September to December (2024)
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Leg length (in cm from the anterior superior iliac spine to the medial malleoulus)
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September to December (2024)
|
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Height
Time Frame: September to December (2024)
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Height (in cm)
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September to December (2024)
|
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Previous groin injury.
Time Frame: September to December (2024)
|
Previous groin injury (in the last 3 months)
|
September to December (2024)
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- de Queiroz JHM, Frota JP, Dos Reis FA, de Oliveira RR. Development and Predictive Validation of the Brazilian Adductor Performance Test for Estimating the Chance of Hip Adductor Injuries in Elite Soccer Athletes. Int J Sports Physiol Perform. 2023 Apr 20;18(6):653-659. doi: 10.1123/ijspp.2022-0306. Print 2023 Jun 1.
- Robaina BQ, Medeiros DM, Roberti LS, Franke RA, Baroni BM. The Single Leg Bridge Test does not replace handheld dynamometer hamstring tests in a clinical setting. Phys Ther Sport. 2023 Sep;63:126-131. doi: 10.1016/j.ptsp.2023.08.001. Epub 2023 Aug 6.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- UO2024/01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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