Actively Recruiting
Acceptability and Efficacy of GO MOVE: A Mobile Health Technology for Youth With Unilateral Cerebral Palsy
Led by Texas Scottish Rite Hospital for Children · Updated on 2025-03-10
50
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This trial studies youth aged 3 to 17 years with unilateral cerebral palsy or a similar brain condition causing one-sided upper limb movement difficulties. It aims to learn how acceptable and effective Go Move, a mobile website, is for helping these young participants and their caregivers set goals and choose exercises to reach those goals. The research is led by Texas Scottish Rite Hospital for Children and focuses on supporting goal achievement in this group. Participants will use the Go Move mobile website to follow a personalized home program focused on their goals. They will spend about 1 hour and 15 minutes each week for 6 weeks completing exercises and activities selected through the website. This program is designed to be used at home with caregiver assistance. During the study, participants complete assessments before and after the 6-week program, including the Canadian Occupational Performance Measure to track progress. Optional assessments like the Assisting Hand Assessment may also be done. The study monitors how well participants achieve their goals and how well Go Move is accepted. Participation lasts about 6 weeks plus assessment time.
CONDITIONS
Brief 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 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 restrictions from a physician
- All ethnic and racial groups 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
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - 6 weeks
Participants complete a goal-driven home program to improve upper limb motor function.
Weekly home activities totaling about 1 hour and 15 minutes per week
Duration - Within 2 weeks before and after treatment
Participants undergo assessments before and after the home program to measure progress.
2 visits (pre- and post-intervention assessments)
Trial Site Locations
Total: 1 location
1
Scottish Rite for Children
Frisco, Texas, United States, 75034
Actively Recruiting
Research Team
A
Angela Shierk, PhD
H
Heather Roberts, PhD
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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