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临床试验/NCT03672864
NCT03672864已完成不适用

Parent Therapist Partnership to Provide Early, Intensive Exercise to Enhance Walking Outcomes in Children With Perinatal Stroke

University of Alberta4 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2019年2月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
18
试验地点
4
主要终点
Gross Motor Function Measure (GMFM-66) - change from baseline

研究概览

简要总结

A prospective, single blind, parallel group, randomized control trial to determine if early, intensive lower extremity activity delivered by a physical therapist and a parent in partnership improves gross motor function more than usual care.

详细描述

A mixed-methods randomized controlled trial at 3 healthcare centres: Edmonton, Calgary and Ottawa. The period of participation for each child is 12 months. The Immediate Group will have 3 months of intervention and 9 months follow-up. The Delay Group will be followed for 6 months (waitlist-control period), then given the opportunity to receive the same intervention and followed for 3 months after the intervention.

The intervention will be delivered by clinicians in the rehabilitation centres in partnership with the child's parents. Therapists will provide training 2 days a week and will coach the parents to provide the training at home for 2 days a week.

The intervention is ELEVATE (Engaging the Lower Extremity Via Active Therapy Early) and consists of child-initiated, intensive leg activities for one hour a day, four days a week for 12 weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

Assessing therapists are masked to the child's group assignment.

入排标准

年龄范围
8 Months 至 36 Months(Child)
性别
All
接受健康志愿者

入选标准

  • children ages 8 months to 3 years
  • medical history and physical exam consistent with perinatal stroke
  • hemiparesis in the upper and/or lower extremity
  • parental agreement to adhere to the training and testing schedule

排除标准

  • bilateral motor impairment
  • epileptic seizures that could interfere with training
  • cognitive, behavioural or developmental impairments that preclude participation in the protocol
  • botulinum toxin A injections or surgery in the lower extremities within the previous six months
  • concurrent casting during the intervention phase (including constraint-induced movement therapy with casting)
  • diagnosis associated with neurological/developmental regression
  • parent unable to communicate (verbal and written) in English or French

研究组 & 干预措施

Immediate Group

Experimental

The intervention is intensive exercise, delivered over 12 weeks beginning on admission to the study. The group will then be followed for 9 months post intervention.

干预措施: Intensive exercise (Behavioral)

Delay Group

No Intervention

The group will be followed for 6 months with no intervention. After 6 months the group will be given the opportunity to receive the same intensive exercise intervention as the Immediate group. The group will be followed for 3 months following the intervention.

结局指标

主要结局

Gross Motor Function Measure (GMFM-66) - change from baseline

时间窗: 3 months, 6 months, 9 months, 12 months

A 66 item criterion referenced observational measure of gross motor skills designed for children with cerebral palsy.

次要结局

  • Young Children's Participation and Environment Measure (YC-PEM) - change from baseline(3 months, 6 months, 9 months, 12 months)
  • Ankle joint angle at onset of stretch reflex - change from baseline(3 months, 6 months, 9 months, 12 months)
  • Ankle joint angle at full dorsiflexion - change from baseline(3 months, 6 months, 9 months, 12 months)
  • Resource use questionnaire(12 months)
  • The Pediatric Quality of Life Measure module for cerebral palsy (PedsQL CP) - change from baseline(3 months, 6 months, 9 months, 12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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