Metrological Properties of a Digital Motion Analysis Research Application for Assessing the Motor Abilities and Performance of Children With Cerebral Palsy
Valid-ABLE
1 other identifier
interventional
60
1 country
1
Brief Summary
Cerebral palsy is a common neurological disorder that is the leading cause of motor disability in children. It causes significant motor impairments, affecting various aspects such as fine and gross motor skills, as well as locomotion, which has a major impact on the quality of life of affected children. It is therefore essential to characterize these functional impairments in order to guide clinical decisions and maximize the motor function of affected children. Currently, the assessment of motor function is based on physical examinations and functional scales, such as the Gross Motor Function Classification System, which is specifically designed to assess children with CP. However, movement analysis using optoelectronic systems is considered the gold standard for this assessment, even though these systems have notable limitations (expensive installation, time-consuming use, and use only in a clinical environment, making it difficult to assess motor skills in children's everyday lives). In order to establish a comprehensive and personalized functional diagnosis, it is crucial to evaluate other fundamental motor tasks such as running, jumping, object control, and balance tasks. Recently, innovative markerless motion analysis technologies have been developed that allow analysis using smartphones or tablets outside of healthcare facilities. Therefore, developing an application dedicated to motion analysis for children with cerebral palsy that is easy to access and can be used frequently could yield many significant benefits.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 10, 2026
CompletedFirst Posted
Study publicly available on registry
February 25, 2026
CompletedStudy Start
First participant enrolled
March 18, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 16, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
November 16, 2028
April 17, 2026
April 1, 2026
2.7 years
February 10, 2026
April 14, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Angle (in degrees) of knee flexion in sagittal view during a two-foot vertical jump using digital motion analysis software
We will measure the left and right knees, which will be classified as either the most affected lower limb or the least affected lower limb in the PC group.
Up to 8 months
Angle (in degrees) of knee flexion in sagittal view during a two-foot vertical jump using the Gold Standard system (Motion Capture System).
We will measure the left and right knees, which will be classified as either the most affected lower limb or the least affected lower limb in the PC group.
Up to 8 months
Study Arms (2)
Children with a medical diagnosis of cerebral palsy as defined by SCPE
EXPERIMENTALHealthy volunteers
ACTIVE COMPARATORInterventions
ABILOCO-Kids
GOAL
Interview
Gold standard
Eligibility Criteria
You may qualify if:
- Common to both groups:
- Obtaining free and informed consent from the child and at least one parent
- Children of all genders aged 6 to 18
- Children affiliated with or beneficiaries of a social security system
- For the Cerebral Palsy group:
- Medical diagnosis of CP according to the SCPE (Surveillance of Cerebral Palsy in Europe) definition;
- Unilateral and bilateral impairment;
- Gross Motor Function Classification System (GMFCS) = I to III;
- No major cognitive or visual impairments that limit the performance of motor tasks
- For the control group:
- \- Children free from any disease
- Other volunteers included in the protocol (qualitative analysis only (parents and clinicians)):
- Parent(s) of children with CP included in this study;
- Healthcare professionals and researchers involved in monitoring children with CP and/or evaluating the research application within the framework of this study
You may not qualify if:
- Common to both groups:
- Participants or parent(s) of participants who do not speak French
- Children subject to legal protection measures
- Pregnant or breastfeeding participants
- For the Cerebral Palsy group:
- Presence of a cause of neuro-orthopedic disorders other than CP
- Limiting pain
- Medical or surgical interventions planned between visit 1 and visit 2
- Children with a condition other than cerebral palsy that affects their walking ability
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Chu Dijon Bourgogne
Dijon, 21000, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 10, 2026
First Posted
February 25, 2026
Study Start
March 18, 2026
Primary Completion (Estimated)
November 16, 2028
Study Completion (Estimated)
November 16, 2028
Last Updated
April 17, 2026
Record last verified: 2026-04