Multidirectional Isometric Assessment of the Hip

April 23, 2025 updated by: Pablo Hernandez-Lucas, University of Vigo

Multidirectional Isometric Assessment of the Hip in Young Swimmers

With the exception of the shoulder, the hip is among the most frequently injured areas in swimmers. Despite this, hip injuries are often overlooked in training and prevention programmes. Such neglect can cause significant damage to muscles, particularly the adductors, and the joint itself, potentially requiring arthroscopic surgery or even leading to secondary injuries in related structures such as the knee. Furthermore, hip strength and range of motion directly affect swimmers' underwater kicking speed. Although hip assessments are common in other sports, like football, for injury prevention and performance analysis-both dynamically and isometrically-isometric testing is particularly recommended due to its higher reproducibility.

Therefore, this study aims to validate a multidirectional isometric hip test in swimmers and examine agonist-antagonist muscle ratios in young advanced swimmers.

A comparative analysis will be conducted on 30 elite swimmers. This will include a descriptive analysis of the group and comparative analyses between breaststroke/non-breaststroke swimmers and between genders. Maximum isometric contractions of both lower limbs will be measured using a Chronojump force sensor (Boscosystem, Barcelona, Spain).

Athletes will stand on a step positioned centrally within a rack or cage, either laterally or frontally depending on the movement assessed (ABD-ADD or flexion-extension, respectively). They will grip the appropriate supports with their hands and perform three maximal efforts of each movement lasting 3 seconds, without compensatory actions (any attempt with compensations will be discounted). There will be a 20-second rest between attempts. All three attempts will be recorded.

To assess measurement reliability, tests will be repeated after 48 hours for subsequent comparison.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

55

Phase

  • Not Applicable

Contacts and Locations

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

Study Contact

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Aged between 14 and 18 years.
  • Swimmers who train at least 15 hours weekly.
  • Swimmers who have participated in the national championship this season.

Exclusion Criteria:

  • Swimmers with any current hip or lower limb pathology.
  • Swimmers who have required hip surgery.
  • Swimmers who, for any other reason, are unable to complete an isometric maximal strength test.
  • No ability to perform the Multidirectional Isometric Assessment of the Hip without compensatory movements.
  • Refusal to sign informed consent (or legal guardian's consent for minors).

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

  • Primary Purpose: Diagnostic
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Validation of Isometric Assessment of the Hip in Swimmers
Participants perform isometric tests (flexion, extension, ABD, ADD) to assess isometric hip strength at different basic movements over two sessions. Data is collected to evaluate the reliability and validity of these tests for swimmers.
Participants perform isometric tests (flexion, extension, ABD, ADD) to assess isometric hip strength at different basic movements over two sessions. Data is collected to evaluate the reliability and validity of these tests for swimmers.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intraclass Correlation Coefficient (ICC) for Multidirectional Isometric Test.
Time Frame: Measured at two time points: baseline (Day 0) and follow-up (Day 2).
Assessment of between-day reliability of the Multidirectional Isometric Test using intraclass correlation Coefficients (ICC) for hip flexion, extension, abduction and adduction movements.
Measured at two time points: baseline (Day 0) and follow-up (Day 2).
Coefficient of Variation (CV) for Multidirectional Isometric Test.
Time Frame: Measured at two time points: baseline (Day 0) and follow-up (Day 2).
Analysis of the coefficient of variation (CV) to evaluate data dispersion and consistency for Multidirectional Isometric Test.
Measured at two time points: baseline (Day 0) and follow-up (Day 2).
Minimum Detectable Change (MDC) for Multidirectional Isometric Test.
Time Frame: Measured at two time points: baseline (Day 0) and follow-up (Day 2).
Calculation of the minimum detectable change (MDC) to identify the smallest significant change in performance beyond measurement error for Multidirectional Isometric Test. (MDC90: Minimal Detectable Change at 90% Confidence; MDC%: Minimal Detectable Change Percentage).
Measured at two time points: baseline (Day 0) and follow-up (Day 2).
Force Ratios Between for Multidirectional Isometric Test.
Time Frame: Measured at point baseline (Day 0).
Evaluation of the agonist-antagonist strength ratios between hip flexion, extension, abduction and adduction movements.
Measured at point baseline (Day 0).

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 (Estimated)

April 28, 2025

Primary Completion (Estimated)

May 5, 2025

Study Completion (Estimated)

June 30, 2025

Study Registration Dates

First Submitted

April 13, 2025

First Submitted That Met QC Criteria

April 22, 2025

First Posted (Actual)

April 23, 2025

Study Record Updates

Last Update Posted (Actual)

April 27, 2025

Last Update Submitted That Met QC Criteria

April 23, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • Cadera

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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