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临床试验/NCT06704880
NCT06704880尚未招募不适用

Lower Limb Constraint-induced Movement Training Versus Strength Training of the Non-hemiplegic Lower Limb on Motor Performance in Children With Hemiplegic Cerebral Palsy: A Randomized Control Trial.

Imam Abdulrahman Bin Faisal University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年11月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
40
试验地点
1
主要终点
gait speed

研究概览

简要总结

This clinical trial aims to Compare the effectiveness of lower limb CIMT and the Strength Training of the Non-Hemiplegic lower limb on motor performance in hemiplegic children with CP.

Participants will:

diagnosed with hemiplegic cerebral palsy treated with CIMT or Strength training (cross-education) for a non-hemiplegic limb for 8 weeks.

3 sessions per week. Measurements will be taken at baseline and then at the end of the 8 weeks.

详细描述

Method:

32 children with hemiplegic CP will be equally and randomly allocated to two groups (group A and B). group A will receive lower limb CIMT for the non- hemiplegic limb using whole leg orthosis and Group B will receive strengthen training for the non-hemiplegic lower limb. Both groups will receive routine physical therapy for the hemiplegic lower limb. Both groups will receive 60 minutes training session for 3 sessions per week for 8 consecutive weeks. Assessment will be at baseline then at the end of trial.

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)

入排标准

年龄范围
5 Years 至 15 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Children with hemiplegic cerebral palsy aged age between 4 and
  • •(GMFCS) levels I, II and III.
  • •Able to follow therapist instructions during training session.

排除标准

  • •Lack of patient's cooperation.
  • •Difficulty wearing constraint method due to severe joint deformation or/and contracture.
  • •Patients were treated with botulinum toxin during the last 3 months.
  • •Seizure disorder not fully controlled by medication.

研究组 & 干预措施

CIMT GROUP

Experimental

干预措施: rehabilitation (Other)

STRENGHTH TRAINING GROUP (cross education)

Experimental

干预措施: rehabilitation (Other)

结局指标

主要结局

gait speed

时间窗: at base line then at the end of the 8 weeks

gait spatiotemporal parameter

cadence gait spatiotemporal parameter

时间窗: at base line then at the end of the 8 weeks

gait spatiotemporal parameter

step length

时间窗: at base line then at the end of the 8 weeks

gait spatiotemporal parameter

stride length

时间窗: at base line then at the end of the 8 weeks

gait spatiotemporal parameter

次要结局

  • Pediatric balance scale(at base line then at the end of the 8 weeks)
  • 6 Minute walk test (6MWT)(at base line then at the end of the 8 weeks)
  • Modified Ashworth scale(at base line then at the end of the 8 weeks)
  • Handheld dynamometer(at base line then at the end of the 8 weeks)

研究者

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

Abdullah Owaid Kerdi Alanazi

PHYSIOTHERAPIST

Imam Abdulrahman Bin Faisal University

研究点 (1)

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