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临床试验/NCT07578961
NCT07578961进行中(未招募)不适用

Combined Effects of Tactile Kinesthetic Stimulation With Neural Mobilization on Sensory and Motor Functions of the Upper Limb in Stroke Patients

Riphah International University1 个研究点 分布在 1 个国家目标入组 53 人开始时间: 2025年4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
53
试验地点
1

研究概览

简要总结

Combined Effects of Tactile -kinesthetic stimulation with Neural mobilization on sensory and motor functions of upper limb in stroke patients

详细描述

Stroke ranks among the primary causes of lasting disability, frequently leaving the upper limb weak, numb, or clumsy and thereby curtailing daily independence and overall well-being. Although multiple therapy regimens appear helpful, research to date Meestal tests each method alone, obscuring how paired sensory and motor targets might accelerate recovery. The present study investigates combined the effect of tactile-kinesthetic input with neural mobilization against standard care, hypothesizing that the blend will produce broader gains in sensation and movement.

This randomized clinical trial will be conducted at Ittefaq Hospital (Trust) Lahore and Gulab Devi Chest Hospital Lahore over duration of 11 months. The sample size will be (53) participants. Participants which meet the inclusion criteria will be taken through non-probability convenience sampling technique, which will further be randomized through lottery method. Group A (27) participants will be assigned to combined tactile kinesthetic stimulation plus neural mobilization and Group B (27)participants will be assigned to conventional therapy. Data will be collected through different assessment tools, including Fugyl-Meyer Assessment for motor function, Nottingham Sensory Assessment Scale (NAS) for sensory function. Pre-interventions assessments will be conducted for both groups. The effects of the interventions will be measured at pre-treatment and post-treatment of 6 weeks. Data analysis will be performed by using SPSS 26 software.

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
45 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 45 - 65 years
  • Both gender Male and Female
  • Diagnosed with chronic stroke stated as occurring 6 month to 12 month .
  • Sensory impairment - loss of tactile and proprioception NSA ( < 7/12)
  • Motor impairment - lack in full strength and coordination ( Brunnstrom >3)
  • Scored 24 or higher on the Mini-Mental State Examination, indicating sufficient cognition to follow study instructions.

排除标准

  • Severe cognitive or communication difficulties that would prevent meaningful involvement in therapy or testing.
  • Comorbid conditions that impair upper-limb function, including arthritis, prior fractures, or similar disorders.
  • Neurological conditions other than stroke that could interfere with study outcomes
  • Engagement in any other rehabilitation program during the trial period.

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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