Comparative Effects of Somatosensory Stimulation and Task Based Mirror Therapy in Post Stroke Patients

May 5, 2026 updated by: Riphah International University

Comparative Effects of Somatosensory Stimulation and Task Based Mirror Therapy on Upper Limb Function in Post Stroke Patients

This randomized controlled trial will be conducted at the Department of Physical Therapy, DHQ Hospital Sheikhupura, over duration of eleven months. A total of 20 stroke patients meeting inclusion criteria will be conveniently sampled and randomly assigned into two groups. Group A will receive somatosensory stimulation, while Group B will undergo task-based mirror therapy. Interventions will be administered five times per week for four weeks. Upper limb function will be assessed at baseline and post-intervention using the Fugl-Meyer Assessment for Upper Extremity (FMA-UE), Action Research Arm Test (ARAT), and the Box and Block Test (BBT) to assess upper limb motor function, task based performance and gross motor dexterity. Data analysis will be performed using SPSS version 26.

Study Overview

Status

Active, not recruiting

Study Type

Interventional

Enrollment (Estimated)

24

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Sheikhupura, Pakistan
        • Department of Physical Therapy, DHQ Hospital Sheikhupura

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age: above 40-70 years
  • Both Male and female patients
  • Unilateral ischemic or hemorrhagic stroke
  • Having attack duration of 1 to 6 months
  • Mild - Moderate motor impairment
  • Moderate cognitive ability according to Mini-mental State Examination score >24 3 grade Brunnstrom upper extremity stage

Exclusion Criteria:

  • Aphasia
  • Serious unilateral neglect (Star Cancellation Test ≤ 44/54) or visual field deficiency
  • Any other comorbid neurological diseases except for stroke
  • Diagnosis of any other neuromuscular or orthopedic disease in the upper extremities

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Task based Mirror Therapy
Patients will be administered with Task-Based Mirror Therapy, where they will practice real-life functional movement through a mirror reflection of the movement of the affected upper limb. The mirror will be located with a sagittal angle so that the reflection of the patient only display the image of the non-affected limb, resulting in an optical illusion that both limbs move symmetrically
Patients will be administered with Task-Based Mirror Therapy, where they will practice real-life functional movement through a mirror reflection of the movement of the affected upper limb. The mirror will be located with a sagittal angle so that the reflection of the patient only display the image of the non-affected limb, resulting in an optical illusion that both limbs move symmetrically
Experimental: Somatosensory Stimulation
The group will be provided with somatosensory stimulation-induced rehabilitation of the upper limb, which will personalize to patients with both motor and sensory disturbance after stroke. The aim of the therapy will be to improve the functioning of upper limbs that focused directly on tactile, proprioceptive, and sensory discrimination abilities (14). The session will be started with a 5-minute warm-up, and the muscle groups involved active-assisted movement of the shoulder, elbow, and wrist to achieve better circulation and excite the limb to receive the sensations. Patients will be advised to direct their attention to the kinaesthetics of motion.
The group will be provided with somatosensory stimulation-induced rehabilitation of the upper limb, which will personalize to patients with both motor and sensory disturbance after stroke. The aim of the therapy will be to improve the functioning of upper limbs that focused directly on tactile, proprioceptive, and sensory discrimination abilities (14). The session will be started with a 5-minute warm-up, and the muscle groups involved active-assisted movement of the shoulder, elbow, and wrist to achieve better circulation and excite the limb to receive the sensations. Patients will be advised to direct their attention to the kinaesthetics of motion.
Other Names:
  • somatosensory stimulation-induced rehabilitation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
BOX & BLOCK TEST
Time Frame: 4th Week
The Box and Block Test (BBT) is a performance-based measure of gross manual dexterity that allows clinicians to infer about levels of activity
4th Week
ACTION RESEARCH ARM TEST
Time Frame: 4th Week
Action research arm test has been used widely clinically for the assessment of upper extremity function post stroke and in various other conditions. Measurement of recovery after stroke is becoming increasingly important with the advent of new treatment options under investigation in stroke rehabilitation research.
4th Week

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Fugl-Meyer Assessment for Upper Extremity (FMA-UE)
Time Frame: 4th week
The Fugl-Meyer Assessment of Upper Extremity (FMA-UE) is recommended for evaluation of sensorimotor impairment post stroke, but the item-level reliability of the scale is unknown. The FMA-UE is reliable both within and between raters in patients with stroke in the early subacute phase. A wider international use of FMA-UE will allow comparison of stroke recovery between regions and countries and thereby potentially improve the quality of care and rehabilitation in persons with stroke worldwide.
4th week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Zain Ul Abbas, Ms, Riphah International University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 1, 2025

Primary Completion (Estimated)

May 1, 2026

Study Completion (Estimated)

July 1, 2026

Study Registration Dates

First Submitted

May 5, 2026

First Submitted That Met QC Criteria

May 5, 2026

First Posted (Actual)

May 11, 2026

Study Record Updates

Last Update Posted (Actual)

May 11, 2026

Last Update Submitted That Met QC Criteria

May 5, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Stroke

Clinical Trials on Mirror Therapy:

Subscribe