Growth Process and Development of the Musculoskeletal System in Young Gymnasts

April 14, 2024 updated by: Gali Dar, University of Haifa

Growth Process and Development of Muscle, Bone, and Tendon in Correlation With Injuries in Young Gymnasts During Adolescence

assessment of the musculoskeletal system will be performed twice a year, for three years of young gymnasts.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

Aims: To examine the changes in the anatomical and morphological features in the skeleton of young female artistic and rhythmic gymnasts and follow the risk of injuries during the period of pubertal growth.

Methods: 200 gymnasts (100 rhythmic and 100 artistic) will participate. Measurements will be performed at the beginning and the end of each year, for three years. Each gymnast will be examined for the following: asked about her menarche, assessed by a physician for Tanner stages, and will answer the Triad-specific self-report questionnaire. Anthropometric measurements (height, weight, BMI), muscle strength (using hand-held dynamometer), joint range of motion (using goniometer), scoliosis, and Beighton test for hypermobility will be assessed. In addition, the gymnasts will be scanned by using three different ultrasounds: Bone age for the skeletal age, SOS for the bone properties, and ultrasound tissue characterization for the tendon structure. The gymnasts will be asked about their physical training history, frequency, and training intensity. Each gymnast will be asked whether she had pain or injuries during the period she has been training, as well as a physical and injuries evaluation that will be conducted by a physician.

Once a month a telephone follow-up with the trainer regarding any pain or injuries in the last month will be conducted.

Study Type

Observational

Enrollment (Estimated)

200

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

Study Contact Backup

  • Name: Da

Study Locations

      • Netanya, Israel
        • Recruiting
        • The Academic college Levinsky-Wingate at the Wingate Institute

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

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

young female gymnasts training on a regular basis and competitive level

Description

Inclusion Criteria:

  • training at least 4 times per week,
  • a minimum of 16 hours per week, at a competitive level.
  • The gymnasts exercised fully three months before the beginning of the study
  • have not been absent more than three days from training due to pain, discomfort, or injury.

Exclusion Criteria:

  • present injury causing pain
  • missing training.

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
gymnasts
gymnasts ages 9-16 years. All participants are of competitive level, each participating in at least four competitions per year
examination of tendon, muscle joints and injuries

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
ultrasound tissue characterized
Time Frame: baseline, twice a year for 3 years
percentage of type 1,2,3,4 fibers within the tendon
baseline, twice a year for 3 years
muscle strength test
Time Frame: baseline, twice a year for 3 years
hand held dynamometer assessment of ankle, knee and hip muscles
baseline, twice a year for 3 years
range of motion
Time Frame: baseline, twice a year for 3 years
goniometer assessment for lower extremities joints
baseline, twice a year for 3 years
bone strength
Time Frame: baseline, twice a year for 3 years
tibia bone strength assessment using Sunlight MiniOmni Ultrasound Bone Sonometer
baseline, twice a year for 3 years
Bone Age
Time Frame: baseline, twice a year for 3 years
bone age of the radius bone using ultrasound for bone age
baseline, twice a year for 3 years

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Gali Dar, University of Haifa

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)

January 1, 2024

Primary Completion (Estimated)

March 15, 2026

Study Completion (Estimated)

March 15, 2026

Study Registration Dates

First Submitted

March 12, 2024

First Submitted That Met QC Criteria

March 12, 2024

First Posted (Actual)

March 19, 2024

Study Record Updates

Last Update Posted (Actual)

April 16, 2024

Last Update Submitted That Met QC Criteria

April 14, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • ADINEGEV-2021_102

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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