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临床试验/NCT03672877
NCT03672877招募中不适用

Randomized Controlled Trial of Early Intensive Leg Exercise to Improve Walking in Children With Diplegia From Encephalopathy of Prematurity

University of Alberta4 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年1月28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
60
试验地点
4
主要终点
Change in Gross Motor Functional Measure - 66 Items (GMFM-66)

研究概览

简要总结

This is a randomized controlled trial, comparing 3 months of intensive leg exercise to standard physiotherapy care for the improvement of gross motor function in young children with spastic diplegia.

详细描述

Children born prematurely are at risk of brain injury that can result in cerebral palsy, most often affecting both legs. Current treatment is largely passive, including leg braces, repeated injection of a paralyzing agent (botulinum toxin) in muscles that are abnormally active, and surgery as deformities occur. Active, physical therapy for weak muscles is infrequent, occurring twice a month or less. Yet, recent work in mammals show that early brain injury can be alleviated by intensive exercise therapy, but only while the animal is very young.

Building on our success with early, intensive therapy for children with perinatal stroke, we will apply intensive therapy for the legs in children with cerebral palsy involving both legs. Children (8 mo - 3 yr old) will be randomly assigned to start treatment immediately or delay treatment for 6 months. The delay period controls for improvement without treatment. The children in the Delay Group will have the option to receive the same treatment after the delay period. The therapy will be guided by physical therapists, and centered on play. Measures will be taken before, during and after the delay and treatment periods. Measures will include clinical scores of motor development, proficiency of walking, participation at home, and physiological measures of motor and sensory function. All children will be followed until they turn 4 yr old, to determine if there are long term benefits. The cost-effectiveness of the intervention will be evaluated by a health economist. We anticipate that early intensive exercise will improve mobility, facilitate earlier and better walking, and that the effects will be enduring.

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

Physical therapy assessors will be blinded 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

  • Bilateral motor impairment of the lower extremities
  • Periventricular white matter injury from encephalopathy of prematurity
  • Able to stand with some support

排除标准

  • Substantial upper extremity involvement - Manual Abilities Classification System (MACS) Level ≥3
  • Uncontrolled epilepsy or infantile spasms in the past 6 months
  • Cardiovascular or musculoskeletal complications that preclude participation in intensive exercise
  • Botulinum toxin-A (BTX-A) injections in the legs in the last 6 months

研究组 & 干预措施

Immediate training group

Experimental

Children will participate in intensive exercise intervention for 3 months and will be followed for 9 months following the intervention

干预措施: Intensive exercise (Behavioral)

Delay training group

No Intervention

Children will be assessed for 6 months with no intervention. After the 6 month period children will be given the same intervention as the immediate group and followed for 3 months after the intervention.

结局指标

主要结局

Change in Gross Motor Functional Measure - 66 Items (GMFM-66)

时间窗: From Baseline to 6 months

This is a 66 item criterion-referenced observational measure to assess change in gross motor function of children with cerebral palsy.

次要结局

  • Change on Pediatric Quality of Life Measure module for cerebral palsy (PedsQL CP)(From Baseline to 6 months)
  • Change in stiffness at the ankle(From Baseline to 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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