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临床试验/NCT07683130
NCT07683130已完成不适用

Comparative Effects of Mirror Therapy, Proprioceptive Neuromuscular Facilitation, and Constraint-Induced Movement Therapy on Upper Limb Motor Recovery in Stroke Survivors: A Three-Arm Randomized Controlled Trial

Foundation of Medical Research and Laboratories, Pakistan1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2025年7月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
90
试验地点
1
主要终点
Action Research Arm Test

研究概览

简要总结

This study aimed to compare the effects of these three interventions on upper limb motor recovery in stroke survivors.

A three-arm randomized controlled trial was conducted in which eligible participants (N=90) with post-stroke upper limb hemiparesis were randomly allocated into three groups of 30 each: MT group, PNF group, and CIMT group. All groups received their respective interventions alongside conventional physiotherapy, five sessions per week for six weeks.

详细描述

Stroke remains a leading cause of long-term disability worldwide, with upper limb motor impairment being one of the most prevalent and debilitating consequences. While several neurorehabilitation approaches have demonstrated efficacy individually, limited evidence existed comparing the relative effectiveness of mirror therapy (MT), proprioceptive neuromuscular facilitation (PNF), and constraint-induced movement therapy (CIMT) within a single trial framework. This study aimed to compare the effects of these three interventions on upper limb motor recovery in stroke survivors.

A three-arm randomized controlled trial was conducted in which eligible participants (N=90) with post-stroke upper limb hemiparesis were randomly allocated into three groups of 30 each: MT group, PNF group, and CIMT group. All groups received their respective interventions alongside conventional physiotherapy, five sessions per week for six weeks. The outcome measure were the Fugl-Meyer Assessment for Upper Extremity (FMA-UE), Action Research Arm Test (ARAT), Modified Ashworth Scale (MAS) and grip strength via hand-held dynamometry. Assessments were performed at baseline and at after 12 weeks post-intervention.

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 (Participant)

入排标准

年龄范围
25 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Stroke Patients Both male and female Age: 25-65 years -

排除标准

  • unable to perform exercises Do not provide consent Cognitive Impairment

结局指标

主要结局

Action Research Arm Test

时间窗: 12 weeks

The assessment were taken at baseline and after 12 weeks of intervention

Fugl-Meyer Assessment for Upper Extremity

时间窗: 12 weeks

The assessment were taken at baseline and after 12 weeks of intervention

Modified Ashworth Scale

时间窗: 12 weeks

The assessment were taken at baseline and after 12 weeks of intervention

grip strength via hand-held dynamometry

时间窗: 12 weeks

The assessment were taken at baseline and after 12 weeks of intervention

次要结局

未报告次要终点

研究者

发起方
Foundation of Medical Research and Laboratories, Pakistan
申办方类型
Other
责任方
Sponsor

研究点 (1)

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