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Clinical Trials/NCT06069765
NCT06069765
Not Yet Recruiting
N/A

Trunk and Upper Extremities Program Effect in Decreasing Compensation Patterns in Unilateral Cerebral Palsy Children: Randomized Control Trial

Fundacio Aspace Catalunya0 sites40 target enrollmentSeptember 2025

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cerebral Palsy Infantile
Sponsor
Fundacio Aspace Catalunya
Enrollment
40
Primary Endpoint
Rate of variance of the Compensation patterns
Status
Not Yet Recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this clinical trial is to test the effectiveness of a trunk and upper extremities exercise program. The main questions it aims to answer are:

Whether the program decreases compensation patterns in unilateral cerebral palsy children Whether the program decreases pain in unilateral cerebral palsy children Whether the program improves bimanual ability in unilateral cerebral palsy children Participants will undertake and 8-week program exercise at home If there is a comparison group: Researchers will compare with the control group to see if this program decreases compensation patterns.

Detailed Description

Children in control group will continue with their daily activities. Children in experimental group, apart from their daily activities, will undertake an 8-week program exercise at home for strengthening the trunk and the proximal part of both upper extremities. It contains 3 progressions that can be applied if needed.

Registry
clinicaltrials.gov
Start Date
September 2025
End Date
July 2027
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Fundacio Aspace Catalunya
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Unilateral cerebral palsy diagnostic
  • Level I or II of the Manual Ability Scale Classification

Exclusion Criteria

  • Have received any intervention with botulinum toxin or shock waves in the previous six months or have them scheduled during the intervention
  • Are undergoing treatment with intensive therapies.
  • To have known alteration in the hips
  • Have very serious attention or comprehension difficulties that prevent them from following instructions.
  • Suffer uncontrolled epilepsies
  • Suffer from severe visual problems.

Outcomes

Primary Outcomes

Rate of variance of the Compensation patterns

Time Frame: 8 weeks

DeepLabCut (DLC) (Artificial Intelligence). Calculate the kinematic difference of the body marks during the activities

Secondary Outcomes

  • Intensity of pain(8 weeks)
  • Location of pain(8 weeks)
  • Bimanual ability(8 weeks)

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