Actively Recruiting

Phase Not Applicable
Age: 45Years - 60Years
All Genders
NCT07139002

Combined Effect of Sensory Training With Bobath Therapy in Patients With Chronic Stroke

Led by Riphah International University · Updated on 2025-08-24

40

Participants Needed

1

Research Sites

47 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic stroke causes moderate to severe impairments in proprioception, balance, and motor functions, which can impact upon an individual's ability to perform activities of daily living, leading to reduced quality of life and increased dependency. Proprioception, or detecting the body's position in open space, is important for balance and coordinated movement. One therapy uses traditional rehabilitation methods like Bobath theory to increase motor functions, aiming to utilize sensory and movement facilitation. Nonetheless, combining sensory and Bobath therapy could lead to superior outcomes by simultaneously addressing both the proprioceptive deficit and motor skills. The purpose of this project is to explore the combined effect of sensory training and Bobath therapy on proprioception, balance, andmotor function in chronic stroke survivors.

CONDITIONS

Official Title

Combined Effect of Sensory Training With Bobath Therapy in Patients With Chronic Stroke

Who Can Participate

Age: 45Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Both male and female included.
  • Age group: 45 years to 60 years.
  • Participants diagnosed with chronic stroke 6 months to 2 years.
  • Mini-Mental State Examination (MMSE) score of 24 or higher.
  • Cannot maintain balance for 30 seconds.
  • Ambulate independently for 7 meters.
Not Eligible

You will not qualify if you...

  • Participants having conditions other than chronic stroke (Parkinson's disease, Alzheimer's disease, orthopedic pathological condition, etc.).
  • Participants having any visual, vestibular, or auditory impairment.
  • Participants having any muscular injuries in the previous 6 months.
  • Participants with a history of fracture in the previous 6 months.
  • Participants with a history of mental illness.
  • Participants with cardiovascular complications.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ittefaq Hospital (Trust), Lahore

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

A

Asrar Yousaf, M.phill

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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