Sensorimotor training vs. dual-task training for chronic stroke patients
Official title: Comparative Effects of Sensorimotor Training and Dual-Task Training on Proprioception, Balance, Functional Mobility and Fall Risk in Stroke Patients
Run by Riphah International University · NCT07628374 · Data updated 2026-11-12
This trial tests whether sensorimotor training or dual-task training improves proprioception, balance, and mobility in people who are more than 6 months post-stroke.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 40 Years to 60 Years |
| Sex | All |
| Enrollment | 54 (estimated) |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Rajanpur, Punjab Province) |
| Status | Recruiting |
| Started | April 20, 2026 |
| Main results expected | July 5, 2026 |
| Study ends | July 20, 2026 |
| Registry record updated | June 5, 2026 |
| Trial ID | NCT07628374 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with chronic stroke (≥6 months), able to walk at least 10 minutes, with balance impairment (Mini-BESTest ≤ 21) and adequate cognition (MoCA ≥ 21).
✕Probably not a fit
Individuals with severe musculoskeletal issues, aphasia, unstable cardiopulmonary conditions, active psychiatric disorders, non-community dwelling before stroke, or recent participation in similar rehab studies may see limited benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized clinical trial compares two rehabilitation approaches—sensorimotor training and dual-task training—in adults with chronic stroke. Participants will be randomly assigned to one of three groups and receive targeted exercises alongside conventional physical therapy. The study aims to measure changes in proprioception, balance, functional mobility, and fall risk using standardized assessments. Recruitment will enroll 54 community-dwelling adults from hospitals in Rajanpur and Multan, Pakistan, with balanced allocation via sealed envelopes.
Why it matters
Potential benefit: If successful, participants may experience improved balance, mobility, and reduced fall risk, contributing to greater independence.
How similar studies have gone: Previous work in stroke rehabilitation supports benefit from both sensorimotor and cognitive-motor training approaches, though direct head-to-head comparison in chronic stroke is less common.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * A diagnosis of stroke; ≥6 months after stroke onset * Able to walk independently for at least 10 minutes * Mini-BESTest score ≤21 indicating balance impairment. * MoCA score ≥21 to confirm adequate cognitive function Exclusion Criteria: * Severe musculoskeletal conditions (e.g., advanced osteoarthritis, recent fractures) that significantly affect mobility or balance. * Significant receptive or expressive aphasia * Unstable heart or lung conditions preventing exercise. * Active psychiatric disorders (e.g., major depression, schizophrenia) * Not community-dwelling before the stroke event * Involved in similar rehab or studies within the last 3 months
Where it's running
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DHQ Rajanpur
Rajanpur, Punjab Province, Pakistan Recruiting
Study contacts
- Principal investigator: Sabiha Arshad — Riphah International University
- Study coordinator: Imran Amjad
- Email: imran.amjad@riphah.edu.pk
- Phone: +923324490125
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Remote Ischaemic Conditioning for Fatigue After Stroke 2
Aat least 12 weeks after stroke, adults with post-stroke fatigue will try a simple hand-arm cuff treatment at home to see if it helps reduce fatigue.
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Dual-task balance training plus computer-based cognitive training after stroke
In adults who recently had a stroke, the study tests whether adding computerized cognitive exercises to balance training improves balance and other recovery outcomes.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.