Actively Recruiting
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
Eligibility Criteria
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
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
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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