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临床试验/NCT06048419
NCT06048419招募中不适用

Acceptability and Efficacy of GO MOVE: A Mobile Health Technology for Youth With Unilateral Cerebral Palsy

Texas Scottish Rite Hospital for Children2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年2月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
2
主要终点
Canadian Occupational Performance Measure (COPM)

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
3 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 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
  • MACS levels 1-
  • 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).

排除标准

  • 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.

研究组 & 干预措施

Go Move Home Program

Experimental

Goal driven home program

干预措施: Home Program (Behavioral)

结局指标

主要结局

Canadian Occupational Performance Measure (COPM)

时间窗: within 2 weeks of start of intervention (pre-intervention), within 2 weeks of end of intervention (post-intervention)

The Canadian Occupational Performance Measure is a criterion referenced, individualized, client-centered outcome measure designed for use by occupational therapists to detect change in a client's self-perception of occupational performance over time on a scale of 1-10 (1 being the lowest)

次要结局

  • Goal Attainment Scale (GAS) Light(within 2 weeks of start of intervention (pre-intervention), within 2 weeks of end of intervention (post-intervention))
  • Assisting Hand Assessment (AHA) (optional)(within 2 weeks of start of intervention (pre-intervention), within 2 weeks of end of intervention (post-intervention))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Angela Shierk

Clinical Scientist

Texas Scottish Rite Hospital for Children

研究点 (2)

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Acceptability and Efficacy of GO MOVE | 临床试验