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NCT07646418Recruiting

Combined Effects of LIRT-BFR Therapy in Post- Stroke Patients

Combined Effects of Low Intensity Resistance Training With Blood Flow Restriction Therapy on Upper Limb Strength, Forward Reach and Sensorimotor Function in Post-Stroke Patients

Source: ClinicalTrials.gov · Last updated 12 Jun 2026

Brief summary (registry, in English)

Stroke is a focal neurological deficit of sudden onset, with symptoms lasting more than 24 hours leading to consequences like impacting physical abilities, cognitive functions and emotional well-being, speech and language difficulties. Among various rehabilitation program, Blood flow restriction (BFR) therapy with low intensity resistance training has shown its promising results. Blood flow restriction training, also called Kaatsu, originated in Japan. So this study aims to determine the combined effects of Low Intensity Resistance Training with Blood Flow Restriction Therapy on Upper Limb Strength, Forward Reach and Sensorimotor function in Post-Stroke Patients.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
64 (estimated)
First submitted
8 Jun 2026
Start date
1 Jun 2025
Primary completion date
30 Jun 2026
Lead sponsor
Riphah International University
Diseases
Stroke
NCT number
NCT07646418

What you commit to

  • Study type: Interventional
  • Planned participants: 64
  • From 1 Jun 2025 to the primary completion date, 30 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • • People with a history of mental/cognitive illness (9)
    • History of transient ischemic attack (TIA) or recurrent stroke (8)
    • Diabetes with peripheral neuropathy (5)
    • Having resting blood pressure above 160/100 mmHg even after taking medications
    • Cardiovascular comorbidity (heart failure, unstable angina, aortic stenosis)

Who the study is looking for

  • • 50 to 70 year of age (5)
    • Both males and females (5)
    • Generalized stroke population (both ischemic and hemorrhagic stroke) (9).
    • Post stroke patient after 1 month (5)
    • Barthel index scores ≥ 20 (10)
    • Spasticity level according to Modified Ashworth scale should be 1/+1 grade in the affected upper limb(7)
    • Muscle strength at grade 3 according to MMT of affected upper limb (7)

Age in the registry: 50 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Amin Welfare & Teaching Hospital
Coordinator of this site? Confirm its status
SialkotPakistanRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.