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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-09-30

Study Completion Date

2026-12-31

Brief Summary

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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

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Detailed Description

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The children are recorded performing 3 sets of shoulder movements (abduction, adduction, flexion, extension, external rotation 1, external rotation 2, internal rotation 2), first on the left and then on the right, at maximum active range of motion, chosen active range of motion, and maximum passive range of motion. The recordings are made by an RGB-D camera connected to a software (ShoulderLoc from B-com) equipped with artificial intelligence that, after image processing, determines the joint range angle of the shoulder for the given movement. This value is compared to the visual estimation of the examiner and its measurement using a goniometer. The hand-mouth, hand-neck, and internal rotation 1 movements are also performed and compared with the data from the modified Mallet classification.

Conditions

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Clinical Examination of the Shoulder Video-assisted Clinical Examination

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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.