Comparing an Adductor Fatigue Strength Test with Handheld Dynamometry

February 7, 2025 updated by: Hugo Olmedillas Fernandez, University of Oviedo

Evaluation of Hip Muscle Strength: Utility of an Adductor Fatigue Test to Substitute Handheld Dynamometry

The strength of the adductor muscles in a population of federated athletes will be measured using two tests: First, the maximum strength test, utilizing handheld dynamometry. Subsequently, endurance strength will be measured with the Adductor Fatigue Test (Brazilian Adductor Performance Test), in order to evaluate a possible correlation between the two tests.

Study Overview

Status

Completed

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

Observational

Enrollment (Actual)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Asturias
      • Oviedo, Asturias, Spain, 33007
        • Escuela Profesional de Medicina de la Educación Fisica y el Deporte

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Competitive athletes without groin injury in the last 3 months.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Healthy athletes
Competitive athletes without any groin injury.
There is no intervention group.

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)
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.
September to December (2024)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Weight
Time Frame: September to December (2024)
Weight (kg)
September to December (2024)
Hip and groin outcome score (HAGOS)
Time Frame: September to December (2024)
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.
September to December (2024)
Age
Time Frame: September to December (2024)
Age (in years)
September to December (2024)
Sex
Time Frame: September to December (2024)
Biological sex
September to December (2024)
Leg length
Time Frame: September to December (2024)
Leg length (in cm from the anterior superior iliac spine to the medial malleoulus)
September to December (2024)
Height
Time Frame: September to December (2024)
Height (in cm)
September to December (2024)
Previous groin injury.
Time Frame: September to December (2024)
Previous groin injury (in the last 3 months)
September to December (2024)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 11, 2024

Primary Completion (Actual)

February 5, 2025

Study Completion (Actual)

February 6, 2025

Study Registration Dates

First Submitted

August 3, 2024

First Submitted That Met QC Criteria

August 13, 2024

First Posted (Actual)

August 16, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 7, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • UO2024/01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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.

Clinical Trials on Groin Injury

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