Adductor Strength in Athletes Suffering a Groin Injury

September 26, 2022 updated by: Hugo Olmedillas Fernandez, University of Oviedo

Adductor Strength Assessment With Different Procedures for Athletes Suffering a Groin Injury

assess the difference in adductor peak strength evaluated with different instruments. Hand held dynamometer vs force frame

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

This study aims to compare the difference in adductor strength output performed by athletes suffering a groin injury between two different assessment methods. Previous studies have observed that add strength differs depending on the evaluation method. Isometric strength can be measured with hand held dynamometer or with force plates (forceframe). Wether one method is better in order to differenciate adductor strength between healthy and injured limb is not known to date.

Study Type

Observational

Enrollment (Anticipated)

50

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, 33006
        • Recruiting
        • Universidad de Oviedo

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

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

athletes from multidirectional sports (football, basketball, hockey, etc) currently suffering a groin injury

Description

Inclusion Criteria:

  • Suffer a groin injury during the assessment period
  • Accept participating in the study

Exclusion Criteria:

-

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
Injured athletes
Athletes suffering a groin injury
Adductor strength will be evaluated with HHD (handheld dynamometer) and forceplates (Forceframe), both injured leg and healthy will be assess in order to compare both limbs

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
handheld dynamometer strength
Time Frame: november 2022 to june 2023
peak torque measured with the handheld dynamometer the athlete will lay supine with hips flexed at 0º and the examiner will put the forearm between the ankles, the participant has to exert the maximum possible strength with the adductor muscles by squeezing with both legs against the forearm
november 2022 to june 2023
forceframe strength
Time Frame: november 2022 to june 2023
peak torque measured with the forceframe the athlete will lay supine with hips flexed at 0º and the ankles placed by the force plates, the participant has to exert the maximum possible strength with the adductor muscles by squeezing with both legs against the plates
november 2022 to june 2023

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 26, 2022

Primary Completion (ANTICIPATED)

June 1, 2023

Study Completion (ANTICIPATED)

June 2, 2023

Study Registration Dates

First Submitted

September 21, 2022

First Submitted That Met QC Criteria

September 21, 2022

First Posted (ACTUAL)

September 26, 2022

Study Record Updates

Last Update Posted (ACTUAL)

September 29, 2022

Last Update Submitted That Met QC Criteria

September 26, 2022

Last Verified

September 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • UO2022-04

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

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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