Actively Recruiting
Acceptability and Efficacy of GO MOVE
Led by Texas Scottish Rite Hospital for Children · Updated on 2025-03-10
50
Participants Needed
1
Research Sites
145 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn about the acceptability and efficacy of Go Move, a mobile website developed to assist youth with unilateral cerebral palsy and their caregivers with setting goals and selecting exercises and activities to meet the goals. The main question\[s\] it aims to answer are: * Is Go Move accepted by youth with unilateral cerebral palsy and their caregivers? * Does Go Move support goal attainment for youth with unilateral cerebral palsy? Participants will set up and participate in a goal-driven home program using the Go Move mobile website. Participants will spend 1 hour and 15 minutes per week for 6 weeks working on their home program and will complete pre-intervention and post-intervention assessments.
CONDITIONS
Official Title
Acceptability and Efficacy of GO MOVE
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of unilateral cerebral palsy or a non-progressive brain lesion, injury, or trauma causing unilateral upper limb motor impairment
- GMFCS levels 1 or 2
- MACS levels 1 to 3
- Age between 3 and 17 years old
- Ability to follow directions and complete the assessment protocol
- Ability to access the GO MOVE webpage on a personal device
- Ability to participate in everyday activities without medical restrictions throughout the study
- All ethnic and racial groups are eligible
You will not qualify if you...
- Uncontrolled epilepsy
- Significant visual impairment
- Severe behavioral problems
- Inability to complete the assessment protocol or home program
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Scottish Rite for Children
Frisco, Texas, United States, 75034
Actively Recruiting
Research Team
A
Angela Shierk, PhD
CONTACT
H
Heather Roberts, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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