Effects of Task-Based Mirror Therapy for Post-stroke Shoulder-Hand Syndrome
Effects of Task-based Mirror Therapy on Edema, Pain and Upper Limb Motor Function for Post-stroke Shoulder-hand Syndrome
1 other identifier
interventional
34
1 country
2
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable stroke
Started Nov 2025
Shorter than P25 for not_applicable stroke
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 5, 2025
CompletedFirst Submitted
Initial submission to the registry
December 8, 2025
CompletedFirst Posted
Study publicly available on registry
February 24, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 12, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedFebruary 24, 2026
February 1, 2026
5 months
December 8, 2025
February 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Numeric pain rating scale (NPRS)
The Numeric Pain Rating Scale (NPRS) is an effective tool for assessing pain intensity in stroke patients, utilizing a scale from 0 to 10, where 0 indicates "no pain" and 10 represents "the worst pain imaginable." This scale is particularly valuable in stroke populations due to its simplicity and quick administration, allowing for effective communication of pain levels even in individuals with cognitive or physical impairments.
Baseline
Numeric Pain Rating Scale (NPRS)
The Numeric Pain Rating Scale (NPRS) is an effective tool for assessing pain intensity in stroke patients, utilizing a scale from 0 to 10, where 0 indicates "no pain" and 10 represents "the worst pain imaginable." This scale is particularly valuable in stroke populations due to its simplicity and quick administration, allowing for effective communication of pain levels even in individuals with cognitive or physical impairments.
4 weeks
Secondary Outcomes (4)
Figure of 8 measurement method
Baseline
Figure of 8 measurement method
4 weeks
Functional independence measure [FIM]
Baseline
Functional Independence Measure (FIM)
4 weeks
Study Arms (2)
Experimental Group A
EXPERIMENTALTask based mirror therapy
group B
ACTIVE COMPARATORConventional exercises
Interventions
Group A 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
Group B 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
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Alara healthcare clinic
Lahore, Punjab Province, Pakistan
Ittefaq Hospital and Trust Lahore
Lahore, Punjab Province, Pakistan
Related Publications (5)
Lee JI, Kwon SW, Lee A, Tae WS, Pyun SB. Neuroanatomical correlates of poststroke complex regional pain syndrome: a voxel-based lesion symptom-mapping study. Sci Rep. 2021 Jun 22;11(1):13093. doi: 10.1038/s41598-021-92564-7.
PMID: 34158602BACKGROUNDLi L, Li J, He M. Treatment outcomes in post-stroke shoulder-hand syndrome: The role of combined acupuncture, traditional Chinese herb hot compress and rehabilitation training. J Back Musculoskelet Rehabil. 2024;37(4):1023-1030. doi: 10.3233/BMR-230267.
PMID: 38517771BACKGROUNDFeng S, Tang M, Huang G, Wang J, He S, Liu D, Gu L. EMG biofeedback combined with rehabilitation training may be the best physical therapy for improving upper limb motor function and relieving pain in patients with the post-stroke shoulder-hand syndrome: A Bayesian network meta-analysis. Front Neurol. 2023 Jan 10;13:1056156. doi: 10.3389/fneur.2022.1056156. eCollection 2022.
PMID: 36703623BACKGROUNDSaha S, Sur M, Ray Chaudhuri G, Agarwal S. Effects of mirror therapy on oedema, pain and functional activities in patients with poststroke shoulder-hand syndrome: A randomized controlled trial. Physiother Res Int. 2021 Jul;26(3):e1902. doi: 10.1002/pri.1902. Epub 2021 Mar 6.
PMID: 33675672BACKGROUNDLiu H, Xu Y, Jiang W, Hu F, Zhou Y, Pan L, Zhou F, Yin Y, Tan B. Effects of task-based mirror therapy on upper limb motor function in hemiplegia: study protocol for a randomized controlled clinical trial. Trials. 2024 Apr 11;25(1):254. doi: 10.1186/s13063-024-08081-1.
PMID: 38605413BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Binash Afzal, PHD
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 8, 2025
First Posted
February 24, 2026
Study Start
November 5, 2025
Primary Completion
April 12, 2026
Study Completion
April 30, 2026
Last Updated
February 24, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share