Comparative Effects of Sensory Augmentation and Neuromodulation on Enhancing Motor Recovery Among Stroke Survivors
Recruiting
N/A
Interventional Study
Stroke (CVA) or Transient Ischemic Attack
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 45 – 56
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 36 (estimated)
- Sponsor
- Lahore University of Biological and Applied Sciences · Other
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
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 reha…
Trial Locations
Loading…
Loading trial locations…
Eligibility Criteria
Inclusion Criteria:
* Age: 45-65
* Gender: both male and female
* Ischemic stroke
* Diagnosed cases of middle cerebral artery stroke by neurologist
* Stage of recovery - Chronic (more than 6 months)
* Burnstromm recovery stage 3
* Good Compliance
Exclusion Criteria:
* Vestibular Dysfunction
* Ser…
Contacts