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Mirror therapy for shoulder-hand syndrome after a stroke

Tests task-based mirror therapy for swelling, pain and arm movement after stroke.

Plain-language title generated from the registry record
Registry title: Effects of Task-Based Mirror Therapy for Post-stroke Shoulder-Hand Syndrome

Key facts

Where
Lahore, PakistanSee the 2 sites

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for people aged 45 to 75 who had a stroke less than 6 months ago and have shoulder-hand syndrome. It tests mirror therapy for swelling, pain and arm movement.

Age
45 to 75 years
Sex
Men and women can both join.
Disease stage
Subacute stroke, less than 6 months ago, with stable condition and a stroke severity score above 6 on the NIHSS scale. The affected arm must have a Modified Ashworth scale score of 2 or less.

Main reasons for not taking part

  • Medical problems that prevent taking part in the study
  • Severe apraxia or problems with body sensation
  • Unilateral neglect
  • Severe contractures of the affected shoulder, elbow, wrist or fingers
  • Global or receptive aphasia

Read by machine on 13 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 45 and 75 years old?

Source: NCT07428811, who can take part

Where in Pakistan

  • Alara Healthcare ClinicLahore, PakistanContact: Maha Sahar, MSPT-NMTaking people
  • Ittefaq Hospital and Trust LahoreLahore, PakistanContact: Maha Sahar, MSPT-NMTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Riphah International University
Trial code
NCT07428811
Record updated
24 February 2026
Original description
The study aims to determine the effects of task-based mirror therapy on edema, pain and upper limb motor function with shoulder-hand syndrome in post stroke patients.Read full original descriptionShow less

Effects of Task-based Mirror Therapy on Edema, Pain and Upper Limb Motor Function for Post-stroke Shoulder-hand Syndrome

The study aims to determine the effects of task-based mirror therapy on edema, pain and upper limb motor function with shoulder-hand syndrome in post stroke patients.

This randomized clinical trial will take place at Ittefaq Hospital and Trust Lahore and Alara healthcare clinic, Lahore involving 34 participants aged 45-75 years. Using a non-probability convenience sampling method, participants will be randomly assigned by online randomizing tool into two groups: experimental group (17 participants) and control group (17 participants). Both groups will undergo treatment for 30 minutes a day, five days a week, over four weeks. Each task will be performed by repeating each movement 20 times per set for three sets, with a 2-minute break between sets. There will also be 2-minute intervals between each completed task Outcome measures will include pain intensity assessed by the Numeric Pain Rating Scale (NPRS), edema measured by the figure-of-eight method, and upper limb motor function evaluated using the Functional Independence measure (FIM). Assessments will occur at baseline and post-intervention.

Inclusion: Both male and female patients are included in the study; Subacute stroke patients having stroke less than 6 months are included in this study; Stable participants having a stroke severity score > 6 on National Institute of Health Stroke Scale (NIHSS); Modified Ashworth scale score ≤ 2 of the affected upper extremity; Montreal Cognitive Assessment (MoCA) score ≥ 24; Patients who can sit with or without support; No contractures of the affected shoulder, elbow, wrist and fingers; Participants who have no history of peripheral nerve injury or musculoskeletal disease.

Exclusion: • Participants who have medical problems or co-morbidities that interdict their participation in the study; Patients with severe apraxia, somatosensory problems; Unilateral neglect; Severe contractures of the affected shoulder, elbow, wrist and finger; Participants who show the symptoms of global or receptive aphasia.

ClinicalTrials.gov NCT07428811