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NCT07093983Not yet recruiting

Comparing Two Therapies to Improve Arm Function After Stroke

Coupling Rehabilitation Versus Constraint Induced Movement Therapy in Post Stroke Patients With Upper Limb Impairment

Source: ClinicalTrials.gov · Last updated 3 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This clinical trial aims to compare the effects of coupling rehabilitation and constraint-induced movement therapy (CIMT) on improving arm function, hand skills, and daily activity performance in people who have upper limb weakness after a stroke. Participants will be randomly assigned to one of two groups and receive 12 weeks of therapy, including either CIMT or coupling rehabilitation along with conventional physical therapy. The study will evaluate which method is more effective in restoring movement and independence by using standardized assessments before, during, and after the intervention. The findings may help guide future rehabilitation approaches for stroke survivors

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
80 (estimated)
First submitted
22 Jul 2025
Start date
5 Aug 2025
Primary completion date
1 Apr 2026
Lead sponsor
University of Lahore
Diseases
Stroke
NCT number
NCT07093983

What you commit to

  • Study type: Interventional
  • Planned participants: 80
  • From 5 Aug 2025 to the primary completion date, 1 Apr 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

  • Individuals suffering from unstable angina, symptomatic heart failure, or uncontrolled hypertension
  • Physician determined unstable cardiovascular conditions
  • The patient has been diagnosed as having organ failure, including the heart, kidneys, and lungs
  • Individuals who are experiencing cognitive impairment as a result of neurological conditions other than stroke.

Other

  • Patients with any traumatic musculoskeletal injury to upper limbs

Who the study is looking for

  • Patients suffering from Sub acute stroke
  • Motor function score at Fugl-Meyer Assessment between 40-60
  • Fine motor assessment at Box and Block Test\<20
  • ADL's assessment at Motor Activity Log:
    • Amount of use scale\<2.5 Quality of movement scale\<3
    • \-

Age in the registry: 40 years to 65 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
University of lahore teaching hospital
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

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