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NCT07764939Active, not recruiting

Comparative Effects of CIMT and TOT on Hand Function Recovery in Post Stroke Patients

Comparative Effects of Constraint Induced Movement Therapy and Task-oriented Training on Hand Function Recovery in Post Stroke Patients

Source: ClinicalTrials.gov · Last updated 30 Sept 2026

Brief summary (registry, in English)

This controlled clinical study investigates and compares the effectiveness of CIMT and TOT in improving hand function among post-stroke patients. A total of 48 participants from hospitals in Sialkot will be randomly divided into two groups and receive a 3-week intervention consisting of 15 sessions. Outcomes will be assessed using the 9-Hole Peg Test, Jebsen-Taylor Hand Function Test, and grip strength, and the data will be analyzed using SPSS-21 under a single-blinded design.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
48 (actual)
First submitted
1 Jun 2026
Start date
12 Jul 2025
Primary completion date
Oct 2026
Lead sponsor
Riphah International University
Diseases
Stroke
NCT number
NCT07764939

What you commit to

  • Study type: Interventional
  • Participants enrolled: 48
  • From 12 Jul 2025 to the primary completion date, Oct 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

  • Recurrent or bilateral stroke
  • Severe upper limb impairment
  • Active infections, skin lesions, or wounds on the upper limb

Other

  • Severe spasticity (Modified Ashworth Scale \> 3) or joint contractures
  • Severe aphasia, neglect, or cognitive impairments affecting task performance
  • Joint contractures or orthopedic limitations in the upper limb
  • Severe pain during limb movement
  • Participation in other upper limb rehabilitation programs concurrently

Who the study is looking for

  • Age between 45 and 65 years
  • Both male and female participants
  • First-ever unilateral ischemic or hemorrhagic stroke confirmed by imaging
  • Stroke onset in subacute to chronic phase (\>3 months post-stroke)
  • Medically stable and able to sit independently
  • Voluntary wrist extension of at least 10 degrees and finger extension of at least 10 degrees in the affected hand
  • Mini-Mental State Examination (MMSE) score \> 26
  • No significant pain or spasticity in affected upper limb (Modified Ashworth Scale \< 2)
  • Adequate sitting balance and trunk control for upper limb activities
  • Willingness and availability to complete the full intervention (3 weeks)
  • No significant musculoskeletal impairments (e.g., fractures or arthritis) affecting the upper limb

Age in the registry: 45 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
department of physiotherapy, Allama Iqbal Memorial Teaching Hospital
Coordinator of this site? Confirm its status
SialkotPakistanUnknown status

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