Actively Recruiting

Phase Not Applicable
Age: 45Years - 56Years
All Genders
NCT07266662

Comparative Effects of Sensory Augmentation and Neuromodulation on Enhancing Motor Recovery Among Stroke Survivors

Led by Lahore University of Biological and Applied Sciences · Updated on 2025-12-17

36

Participants Needed

2

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the effectiveness of two rehabilitation techniques-Sensory Augmentation (using mirror therapy) and Neuromodulation (using transcranial direct current stimulation, tDCS)-in improving motor recovery among stroke survivors. Stroke often results in long-term impairments, particularly in upper limb motor function, which is critical for daily activities. Although current rehabilitation strategies help, more effective solutions are needed to enhance recovery. Participants, aged 45-65 with chronic stroke and upper extremity impairments, will be randomized into three groups: Group 1 will receive a combination of sensory augmentation (mirror therapy) and neuromodulation (tDCS) with routine physical therapy; Group 2 will receive sensory augmentation (mirror therapy) with routine physical therapy; and Group 3 will receive neuromodulation (tDCS) with routine physical therapy. The interventions will take place four times a week for 8 weeks, and participants will undergo motor function assessments, including the Fugl-Meyer Assessment and Jebsen-Taylor Test, before and after the intervention. The study will compare the effects of each intervention on motor recovery, specifically focusing on upper limb function and motor control. The findings could lead to improved rehabilitation protocols, offering stroke survivors better therapeutic options and enhancing their quality of life.

CONDITIONS

Official Title

Comparative Effects of Sensory Augmentation and Neuromodulation on Enhancing Motor Recovery Among Stroke Survivors

Who Can Participate

Age: 45Years - 56Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 45 and 65 years
  • Both male and female participants
  • Diagnosed ischemic stroke
  • Stroke involving the middle cerebral artery confirmed by a neurologist
  • Chronic stage of recovery (more than 6 months since stroke)
  • Burnstromm recovery stage 3
  • Good compliance with study requirements
Not Eligible

You will not qualify if you...

  • Vestibular dysfunction
  • Serious cognitive impairment
  • Severe vision problems or visuospatial neglect
  • Spasticity with Modified Ashworth scale greater than 3
  • Upper extremity contractures
  • Upper extremity fractures
  • Orthopedic diseases
  • Neurological conditions other than stroke
  • Recurrence of stroke or epilepsy during the study period
  • Serious systemic impairments or other diseases
  • Refusal to participate in the study

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Lahore University of Biological and Applied Sciences

Lahore, Punjab Province, Pakistan

Not Yet Recruiting

2

Pakistan Society of Rehabilitation and Differently Abled Hospital

Lahore, Punjab Province, Pakistan

Actively Recruiting

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Research Team

S

Syed Asad Ali, Doctor of Physical Therapy

CONTACT

N

Nabeela Dawood, NMPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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