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CIMT+VR for Cerebral Palsy

N/A
Waitlist Available
Research Sponsored by Texas Scottish Rite Hospital for Children
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
* have cerebral palsy (a brain injury that causes muscle movement problems) or are a non-progressive brain injury to the developing brain and have difficulty using one of your arms
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, pre-intervention and immediate post-intervention
Awards & highlights

Summary

This study is being done to compare constraint induced movement therapy (CIMT) to CIMT combined with virtual reality technology (CIMT+VR) and its impact on how the children with unilateral cerebral palsy use their arm. CIMT is an intensive upper limb therapy for children with one sided (unilateral) cerebral palsy where the child wears a constraint (splint or mit) on their dominant hand so that they use the involved (weaker) side to do activities. Both groups will work on using both arms together to complete activities (bimanual training) as a way to transfer newly learned skills with one hand into two handed tasks. Assessments before and after the intervention will include clinical assessments (where a research team member observes the child doing tasks and ask questions), motion capture (where the child's movement is recorded using multiple cameras), and wearable sensors on the wrists (like a watch).

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, pre-intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, pre-intervention for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Assisting Hand Assessment (AHA)
Secondary study objectives
Canadian Occupational Performance Measure Occupational Performance Measure (COPM)
Hypertonia Assessment Tool Assessment Tool (HAT)
ICF Brief Core Set for Cerebral Palsy
+4 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: CIMT+VRExperimental Treatment1 Intervention
The CIMT+VR group will use the VR technology to work on upper limb motor skills for approximately two hours per day (4 of the activities described under Key Information at the beginning of this form) while the CIMT-only group will participate in traditional motor-based task-specific activities. Both the VR games and traditional intervention will target the improvement of the same upper limb domains.
Group II: CIMTActive Control1 Intervention
Both groups will participate in 60 hours of intensive therapy over 10 days at SRC (6 hours per day Monday-Friday) following the established 'Pirate Camp' CIMT protocol. The full protocol can be found at: https://twu.edu/occupational-therapy/Camp-Based-Augmented-CIMT-Guide/. Both groups will participate in child friendly outdoor and indoor activities that promote the use of the involved side for example; parachute games, sock toss, penny pick up.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
CIMT + VR
2021
N/A
~30

Find a Location

Who is running the clinical trial?

Texas Scottish Rite Hospital for ChildrenLead Sponsor
21 Previous Clinical Trials
9,098 Total Patients Enrolled
4 Trials studying Cerebral Palsy
120 Patients Enrolled for Cerebral Palsy
Texas Woman's UniversityOTHER
87 Previous Clinical Trials
5,880 Total Patients Enrolled
1 Trials studying Cerebral Palsy
14 Patients Enrolled for Cerebral Palsy
~6 spots leftby Sep 2025