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Clinical Trials in France / NCT06805162
Active, not recruiting Not applicable

Effect of an Unsupervised Multi-domain Intervention on Injury Risk Reduction in Athletics (I-ReductAI).

NCT06805162 · tracked via the Priya Life Science France tracker
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Phase
Not applicable
Started
2025-02-07
Last updated
2025-04-29

Condition(s) studied

Injury

Investigational drug(s) / intervention(s)

Normal trainingSpecific training

Normal training: Athletes should continue their normal training

Specific training: Athletes should consider i) watching the educational videos on injury prevention, ii) perform the neuro-muscular exercises, iii) practice the techniques against stress and anxiety, and iv) consider the injury prognostic feedback.

Study summary

In athletics, injuries can affect athletes' participation in athletics, their performance and career, but also their health in physical, psychological and social aspects, in the short, medium and long term.

Eligibility

Sex
ALL
Min age
18 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: * be licensed at the French Athletics Federation (FFA) for competition (sprints, hurdles, jumps, throws, combined events, and endurance disciplines), without any counter-indications for competitive athletics activity attested by the license at the FFA; * have daily access to a digital device (smartphone, computer, tablet) with a network connection (public or private). Exclusion Criteria: * Any athlete deprived of liberty or subject to legal protection (guardianship, under curatorship, legal protection).

Primary outcome measure(s)

  • Time (day) until the first Injury-type Complaint related to athletics and resulting in Restricted Participation in athletics (ICRP) — Week 14
    Time in days during which athletes are free of ICRP, between an intervention group and a control group

Trial sites (1)

FacilityCityRegionStatus
Centre Hospitalier Universitaire Saint-Etienne France

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06805162 on ClinicalTrials.gov ↗ ← All trials in France