Recruiting

GO MOVE

Sponsor:

Texas Scottish Rite Hospital for Children

Code:

NCT06048419

Conditions

Cerebral Palsy

Hemiplegic Cerebral Palsy

Eligibility Criteria

Sex: All

Age: 3 - 17

Healthy Volunteers: Not accepted

Interventions

Home Program

Study Details

Brief summary:

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

Cerebral Palsy

Hemiplegic Cerebral Palsy

Study ID

NCT06048419

Start date

Feb 20, 2024

Status verified date

Mar, 2025

Completion date

Dec, 2026

Anticipated

Primary completion date

Sep, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 3 - 17

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Inclusion criteria for participants to enroll in the study include a diagnosis of unilateral CP or a non-progressive brain lesion, injury, or trauma of the developing brain that presents with a unilateral upper limb motor impairment. GMFCS levels 1 or 2. MACS levels 1-3. Age 3-17 years old, ability to follow directions, ability to complete the assessment protocol, and the ability to access the GO MOVE webpage on a personal device. All ethnic/racial groups will be eligible to participate. The ability to participate in everyday activities without restriction from a physician throughout the duration of their participation in the study (does not have restrictions/contraindications following a medical procedure).

Exclusion Criteria:

  • The study will exclude any patients with uncontrolled epilepsy or significant visual impairment. The study will exclude any patient with severe behavioral problems or the inability to complete the assessment protocol or home program.

Study Design

Enrollment

50 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Go Move Home Program

Goal driven home program

Interventions

Home Program

Home program for 6 weeks (1 hr and 15 minutes per week)

Primary outcome measure

  • Canadian Occupational Performance Measure (COPM) [ Time Frame: within 2 weeks of start of intervention (pre-intervention), within 2 weeks of end of intervention (post-intervention) ]

Central Contacts and Locations

Central contacts

Angela Shierk, PhD

4694127172angela.shierk@tsrh.org

Heather Roberts, PhD

214-794-8117hroberts3@twu.edu

Locations

Scottish Rite for Children

Recruiting

Frisco, Texas, United States, 75034

Contacts

Angela Shierk, PhD

469-412-7172angela.shierk@tsrh.org

More Information

Sponsor

Texas Scottish Rite Hospital for Children

Last update posted

Mar 10, 2025

Last verified

Mar, 2025

Keywords

  • home program

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Texas Scottish Rite Hospital for Children on 2025-03-10.