Clinical trial Recruiting at 1 site Interventional Ages 35 to 75

Tele-rehabilitation–based hand therapy vs clinic-based constrained movement therapy for chronic stroke

Official title: TELE-REHABILITATION VERSUS CLINIC-BASED MODIFIED CONSTRAINT-INDUCED MOVEMENT THERAPY FOR UPPER LIMB FUNCTION IN CHRONIC STROKE PATIENTS

Run by University of Lahore · NCT07720609 · Data updated 2026-11-12

A 68-person trial is testing whether delivering modified constraint-induced movement therapy for the affected arm via tele-rehab works as well as in-clinic therapy for people with chronic stroke.

Quick facts

Study typeInterventional
Ages35 Years to 75 Years
SexAll
Enrollment68 (estimated)
SponsorUniversity of Lahore
Academic / other
Locations1 site (Lahore, Punjab Province)
StatusRecruiting
StartedJuly 18, 2026
Main results expectedSeptember 6, 2026
Study endsSeptember 6, 2026
Registry record updatedJuly 22, 2026
Trial IDNCT07720609 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 35–75 years with chronic stroke (≥6 months), moderate motor impairment (modified Ashworth ≥2) and adequate internet access for tele-rehab.

Probably not a fit

Patients without sufficient internet access, significant cognitive or communication barriers, or those already engaging in intensive upper-limb therapy 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, single-center study compares tele-rehabilitation-based modified constraint-induced movement therapy (mCIMT) with traditional clinic-based mCIMT in adults aged 35–75 who are at least 6 months post-stroke. Participants receive heat, stretching, range-of-motion exercises, and task-oriented activities with a constraint mitt on the unaffected arm, three times per week for six weeks, plus a daily home practice target of 4 hours. Outcome assessors are blinded to group assignment. The tele-rehab arm uses supervised virtual sessions and a home program, while the clinic arm delivers the same components in person. Primary endpoints are changes in upper-limb function from baseline to post-treatment.

Why it matters

Potential benefit: If successful, tele-rehabilitation could expand access to effective upper-limb therapy for stroke survivors who cannot regularly attend in-person sessions.

How similar studies have gone: Previous studies support mCIMT in improving arm function; tele-rehab approaches are promising but vary in evidence quality, making this direct comparison valuable.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Participant with age from 35 to 75 years
* Both gender
* Patients after 6 month of stroke.
* Participant with flexion and abduction at shoulder minimum 10-15 degree and 5-10 degree at wrist and thumb/digit.
* Participants with access to a smartphone or laptop with internet connectivity and the ability to use it for tele-rehabilitation sessions.
* Participant with modified ashworth scale score of 2 or higher.
* Participants who have internet access and can also engage in video conferences.

Exclusion Criteria:

* Patient with any neurological issues apart from stroke that might impact motor function.
* Patient who is not able to follow the commands or are unable to cooperate.
* Patient with any autoimmune disorder like rheumatoid arthritis that might impact arm function.
* Patient with history of epilepsy. Participant who are involved in any fitness program that can improve upper extremity function.

Where it's running

  • Shadman Medical Center, Lahore
    Lahore, Punjab Province, Pakistan
    Recruiting

Study contacts

  • Principal investigator: Kainat Tariq, MSPTN — The University of Lahore, Lahore
  • Study coordinator: Kainat Tariq, MSPTN
  • Email: kainattariq06@gmail.com
  • Phone: 03328256500

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.