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Acceptability and Efficacy of GO MOVE

T

Texas Scottish Rite Hospital for Children

Status

Enrolling

Conditions

Cerebral Palsy
Hemiplegic Cerebral Palsy

Treatments

Behavioral: Home Program

Study type

Interventional

Funder types

Other

Identifiers

NCT06048419
STU-2023-0531

Details and patient eligibility

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.

Enrollment

50 estimated patients

Sex

All

Ages

3 to 17 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Go Move Home Program
Experimental group
Description:
Goal driven home program
Treatment:
Behavioral: Home Program

Trial contacts and locations

1

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Central trial contact

Angela Shierk, PhD; Heather Roberts, PhD

Data sourced from clinicaltrials.gov

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