跳至主要内容
临床试验/NCT07626554
NCT07626554进行中(未招募)不适用

Comparative Effects of Constraint Induced Movement Therapy and Hand-Arm Bimanual Intensive Training for Upper Extremity Function in Late Sub-Acute Post-Stroke Patients

Riphah International University1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2025年6月5日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
34
试验地点
1

研究概览

简要总结

This study will compare the effects of Constraint Induced Movement Therapy and Hand-Arm Bimanual Intensive Training on upper extremity function in late sub-acute post-stroke patients. It will be a randomized controlled trial. Eligible participants will be randomly allocated into two groups. One group will receive Constraint Induced Movement Therapy, while the other group will receive Hand-Arm Bimanual Intensive Training. Both groups will also receive standard physiotherapy for mobility and postural control. The intervention will continue for 3 weeks. Outcomes will be assessed at baseline and after the intervention using upper limb function and motor control assessment tools.

详细描述

Stroke commonly affects upper extremity function and may reduce a patient's ability to perform daily activities independently. In the late sub-acute phase after stroke, structured rehabilitation may help improve arm and hand function, motor control, and real-world use of the affected upper limb. Constraint Induced Movement Therapy encourages use of the affected upper limb by restricting the unaffected arm and providing intensive task-oriented training. Hand-Arm Bimanual Intensive Training focuses on coordinated use of both hands through functional bimanual tasks. This study will compare these two rehabilitation approaches in late sub-acute post-stroke patients. Findings may help guide evidence-based selection of upper limb rehabilitation strategies for improving functional recovery after stroke.

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

The outcome assessor will remain blinded to group allocation during baseline and post-intervention assessments.

入排标准

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

入选标准

  • Adults aged 40 years and above.
  • Diagnosed with unilateral ischemic or hemorrhagic stroke.
  • Stroke duration between 3 to 6 months.
  • Mini-Mental State Examination score of 24 or above.
  • Able and willing to provide informed consent.

排除标准

  • Severe pain in the more affected upper limb on verbal rating scale.
  • Spasticity greater than 3 on the Modified Ashworth Scale in the affected upper limb.
  • Unstable cardiovascular conditions.
  • Any traumatic musculoskeletal injury of the upper limb.

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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