- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06645574
Towards a Health Promotion for Children Engaged in Sport Intensive Practice for a Healthy Adult (PROTEGE)
This project aims to elucidate the complexities of the preventive approach among young people involved in intensive sports activities, providing valuable recommendations to optimize their physical, mental, and social health both in the present and in the long term. The multidisciplinary skills of a team of researchers in sports science and health will contribute their recognized disciplinary expertise through international publications, as well as solid experience in the demands of elite sports, along with a commitment to transferring innovative knowledge toward a preventive approach to sports training.
The main objective is to determine whether a somatotype aligned with the discipline's expectations protects the athlete in terms of self-perception and, consequently, reduces health-risk behaviors. Secondary objectives will include linking somatotype, growth, psychological changes (self-perception), and the emergence of health-risk behaviors or injuries in these young athletes.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Virginie RAMPAL, PhD
- Phone Number: 0033 4 92 03 05 41
- Email: virginie.rampal@hpu.lenval.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Children aged 8 to 15 years old
- Intensive athletes: that is to say they practice a competitive sporting activity with a number of hours of weekly training greater than their age in years.(For example, a 10 year old child will need to train more than 10 hours per week to be included.)
- Sport at an early age
- Obtaining written and signed informed consent from one of the two parents or the holder of parental authority
- Affiliation to a social security system
Exclusion Criteria: menstruation for more than a year at the time of inclusion
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Girls practizing gymnastics 8 to 15 yo
|
Athletes will have 2 times per years prevention examination:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Determine whether a somatotype in harmony with the expectations of the discipline protects the athlete in terms of self-perceptions and, consequently, reduces risky behaviors for her health.
Time Frame: 2 times a year for up to 84 months of follow-up
|
frequency of occurrence of risky behavior depending on the somatotype of the athletes
|
2 times a year for up to 84 months of follow-up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
1. How does the somatotype of athletes change over time and in response to training? Are these modifications uniform among athletes of the same sex practicing the same sport?
Time Frame: 2 times a year for up to 84 months of follow-up
|
The evolution of the somatotype of athletes over time and in response to training Relationship between athlete somatotype and growth acceleration at puberty Self-esteem and perception of physical appearance between athletes conforming and nonconforming to the ideal somatotype of their sport The prevalence of ACAD and excessive training practices among athletes with low self-esteem related to their physical appearance. Correlation between athletes' somatotype and their predisposition to health problems, such as eating disorders and sports injuries |
2 times a year for up to 84 months of follow-up
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- 24-HPNCL-04
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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