Acceptability and Efficacy of GO MOVE

Last updated: March 6, 2025
Sponsor: Texas Scottish Rite Hospital for Children
Overall Status: Active - Recruiting

Phase

N/A

Condition

Cerebral Palsy

Cerebral Palsy (Pediatric)

Cataplexy

Treatment

Home Program

Clinical Study ID

NCT06048419
STU-2023-0531
  • Ages 3-17
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

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

Exclusion

Exclusion Criteria:

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

Study Design

Total Participants: 50
Treatment Group(s): 1
Primary Treatment: Home Program
Phase:
Study Start date:
February 20, 2024
Estimated Completion Date:
December 31, 2026

Connect with a study center

  • Scottish Rite for Children

    Frisco, Texas 75034
    United States

    Active - Recruiting

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