Acceptability and Efficacy of GO MOVE

NCT ID: NCT06048419

Last Updated: 2025-03-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-20

Study Completion Date

2026-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Cerebral Palsy Hemiplegic Cerebral Palsy

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

prospective cohort
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Go Move Home Program

Goal driven home program

Group Type EXPERIMENTAL

Home Program

Intervention Type BEHAVIORAL

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

Interventions

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Home Program

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

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.
Minimum Eligible Age

3 Years

Maximum Eligible Age

17 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Texas Scottish Rite Hospital for Children

OTHER

Sponsor Role lead

Responsible Party

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Angela Shierk

Clinical Scientist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Angela Shierk, PhD

Role: PRINCIPAL_INVESTIGATOR

Scottish Rite for Children

Locations

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Scottish Rite for Children

Frisco, Texas, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Angela Shierk, PhD

Role: CONTACT

4694127172 ext. 1045

Heather Roberts, PhD

Role: CONTACT

214-794-8117

Facility Contacts

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Angela Shierk, PhD

Role: primary

469-412-7172

Other Identifiers

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STU-2023-0531

Identifier Type: -

Identifier Source: org_study_id

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