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NCT07626554Active, not recruiting

CIMT Versus HABIT in Late Sub-Acute Post-Stroke Rehabilitation

Comparative Effects of Constraint Induced Movement Therapy and Hand-Arm Bimanual Intensive Training for Upper Extremity Function in Late Sub-Acute Post-Stroke Patients

Source: ClinicalTrials.gov · Last updated 4 Jun 2026

Brief summary (registry, in English)

This study will compare the effects of Constraint Induced Movement Therapy and Hand-Arm Bimanual Intensive Training on upper extremity function in late sub-acute post-stroke patients. It will be a randomized controlled trial. Eligible participants will be randomly allocated into two groups. One group will receive Constraint Induced Movement Therapy, while the other group will receive Hand-Arm Bimanual Intensive Training. Both groups will also receive standard physiotherapy for mobility and postural control. The intervention will continue for 3 weeks. Outcomes will be assessed at baseline and after the intervention using upper limb function and motor control assessment tools.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
34 (estimated)
First submitted
1 Jun 2026
Start date
5 Jun 2025
Primary completion date
6 Jul 2026
Lead sponsor
Riphah International University
Diseases
Stroke
NCT number
NCT07626554

What you commit to

  • Study type: Interventional
  • Planned participants: 34
  • From 5 Jun 2025 to the primary completion date, 6 Jul 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

  • Unstable cardiovascular conditions.

Other

  • Severe pain in the more affected upper limb on verbal rating scale.
  • Spasticity greater than 3 on the Modified Ashworth Scale in the affected upper limb.
  • Any traumatic musculoskeletal injury of the upper limb.

Who the study is looking for

  • Adults aged 40 years and above.
  • Diagnosed with unilateral ischemic or hemorrhagic stroke.
  • Stroke duration between 3 to 6 months.
  • Mini-Mental State Examination score of 24 or above.
  • Able and willing to provide informed consent.

Age in the registry: 40 years to - · 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
Riphah College of Rehabilitation Sciences
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

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