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Clinical Trials in France / NCT07147478
Starting soon Observational

Video Analysis and Artificial Intelligence for the Analysis of Upper Limb Movement in Children

NCT07147478 · tracked via the Priya Life Science France tracker
Sponsor
Assistance Publique - Hôpitaux de Paris
Phase
Observational
Started
2025-09
Last updated
2025-08-29

Condition(s) studied

Clinical Examination of the ShoulderVideo-assisted Clinical Examination

Study summary

The principle of the study is to compare the data obtained using a shoulder movement analysis software with those obtained during a traditional clinical examination, that is, using a goniometer and the modified Mallet classification

Eligibility

Sex
ALL
Min age
6 Years
Max age
17 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Age between 6 and 17 years old at the time of inclusion * No neurological pathology * No history of upper limb surgery * No upper limb trauma above the hand in the 6 months preceding the examination * Ability to stand for a minimum of 2 minutes * Consent from the child, both parents, and/or legal representatives for participation in a filmed clinical examination. Exclusion Criteria: * Inability to understand the different movements requested.

Primary outcome measure(s)

  • Comparison of a video-assisted clinical examination method with commonly used clinical practices — 1 day
    Perform 2 sets of 7 to 10 shoulder movements, both active and passive, measure mobility angles using a goniometer and the Mallet classification, as well as the ShoulderLoc software and its artificial intelligence program. Compare the averages obtained for each movement using both methods and compare them using an intraclass correlation coefficient (ICC).

Trial sites (1)

FacilityCityRegionStatus
Service de Chirurgie Orthopédique et Réparatrice de l'Enfant - Hôpital Armand Trousseau Paris 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 NCT07147478 on ClinicalTrials.gov ↗ ← All trials in France