Effects of Task-Oriented Training With and Without Rhythmic Auditory Stimulation in Post-Stroke Patients
2026年7月21日 更新者:Riphah International University
Effects of Task-Oriented Training With and Without Rhythmic Auditory Stimulation on Lower Limb Motor Function, Dynamic Balance, Proprioception, Motivation, and Adherence in Post-Stroke Patients
Stroke is one of the leading causes of long-term disability worldwide.
Among survivors, limitations in lower limb motor function, balance, and proprioception significantly affect their independence and quality of life.
There is a growing need for targeted rehabilitation strategies for stroke survivors, who often experience lower limb impairments that limit independence during a highly active stage of life.
Task-oriented training (TOT) helps patients practice real-life movements, while rhythmic auditory stimulation (RAS), such as metronome beats, can guide and improve their timing and coordination.
研究概览
地位
招聘中
条件
详细说明
It will be a single blinded randomized controlled trial.
Non-probability convenience sampling technique will be used to recruit 38 participants aged 40 to 60 years, subacute stage post-stroke from hospitals of Daska and NLH Physio Clinic.
Sealed opaque method will be used to randomly divide into two groups.
Group A will receive TOT along with RAS, while Group B will receive only TOT.
Both groups will participate in supervised 30-minute exercise sessions, including a 10-minute warm-up and cool-down period, five days a week for eight weeks, in addition to 30 minutes of baseline conventional physiotherapy program.
The interventions will focus on lower limb function, balance, proprioceptive training, and motivational engagement.
Tools used for outcome assessment include the Lower Extremity Functional Scale (LEFS) for motor function, Timed Up and Go (TUG) test for dynamic balance, Joint Position Sense (JPS) test for proprioception, Stroke Rehabilitation Motivation Scale (SRMS) for motivation, and the Rehabilitation Adherence Questionnaire (RAQ) for adherence.
Data will be analyzed using SPSS version 25 to compare pre- and post-intervention effects. .
After assessing the normality, if the p-value is greater than 0.05, a parametric test will be applied.
If the p-value is less than 0.05 then a non-parametric test will be applied.
研究类型
介入性
注册 (估计的)
38
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Imran Amjad, PhD
- 电话号码:03324390125
- 邮箱:imran.amjad@riphah.edu.pk
学习地点
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Daska Kalan、巴基斯坦
- 招聘中
- Civil Hospital Daska, Pakistan
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接触:
- Dr. Jansher Mansoori
- 电话号码:03226613232
- 邮箱:qaynatqaynat0@gmail.com
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
接受健康志愿者
不
描述
Inclusion Criteria:
• Age 40-60 years
- First-time ischemic or hemorrhagic stroke
- Subacute stroke (<6 months)
- Brunnstrom stage ≥ 3 (lower limb)
- Able to walk 10 meters independently or with minimal support
- Able to follow simple commands
Exclusion Criteria:
• Severe aphasia
- Other neurological disorders (Parkinson's, TBI)
- Uncontrolled cardiovascular issues (BP > 180 mmHg, arrhythmias)
- Severe visual, auditory, or orthopedic impairments
- Musculoskeletal injuries or medical conditions limiting participation
- Diabetes, hypertension, fractures, surgeries, OA, RA
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Group A - Task-Oriented Training + Rhythmic Auditory Stimulation
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有源比较器:Group B - Task-Oriented Training Only
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Lower Limb Motor Function
大体时间:Baseline and Week 8
|
Lower Extremity Function (LEFS)
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Baseline and Week 8
|
|
Dynamic Balance
大体时间:Baseline and Week 8
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Time up and Go Test
|
Baseline and Week 8
|
|
Proprioception
大体时间:Baseline and post 8 weeks
|
Joint Position Sense Test
|
Baseline and post 8 weeks
|
|
motivation
大体时间:Baseline and post 8 weeks
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Stroke Rehabilitation Motivation Scale (SRMS)
|
Baseline and post 8 weeks
|
|
adherence
大体时间:Baseline and post 8 weeks
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Rehabilitation Adherence Questionnaire (RAQ)
|
Baseline and post 8 weeks
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Aiza Yousaf, MS-OMPT、Riphah International University
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2025年6月1日
初级完成 (估计的)
2026年7月30日
研究完成 (估计的)
2026年8月5日
研究注册日期
首次提交
2026年7月21日
首先提交符合 QC 标准的
2026年7月21日
首次发布 (实际的)
2026年7月24日
研究记录更新
最后更新发布 (实际的)
2026年7月24日
上次提交的符合 QC 标准的更新
2026年7月21日
最后验证
2026年7月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.