NCT07428811

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
34

participants targeted

Target at P25-P50 for not_applicable stroke

Timeline
Completed

Started Nov 2025

Shorter than P25 for not_applicable stroke

Geographic Reach
1 country

2 active sites

Status
recruiting

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

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

December 8, 2025

Completed
3 months until next milestone

First Posted

Study publicly available on registry

February 24, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 12, 2026

Completed
18 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2026

Completed
Last Updated

February 24, 2026

Status Verified

February 1, 2026

Enrollment Period

5 months

First QC Date

December 8, 2025

Last Update Submit

February 23, 2026

Conditions

Keywords

Edemapainshoulder hand syndromeTask based mirror therapyupper limb motor function

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

EXPERIMENTAL

Task based mirror therapy

Other: Task based mirror therapy

group B

ACTIVE COMPARATOR

Conventional exercises

Other: Conventional 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

Experimental Group A

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

group B

Eligibility Criteria

Age45 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

Ittefaq Hospital and Trust Lahore

Lahore, Punjab Province, Pakistan

RECRUITING

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: 34158602BACKGROUND
  • Li 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: 38517771BACKGROUND
  • Feng 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: 36703623BACKGROUND
  • Saha 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: 33675672BACKGROUND
  • Liu 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

StrokeEdemaPainReflex Sympathetic Dystrophy

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsNeurologic ManifestationsComplex Regional Pain SyndromesAutonomic Nervous System DiseasesPeripheral Nervous System DiseasesNeuromuscular Diseases

Study Officials

  • Binash Afzal, PHD

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Maha Sahar, MSPT-NM

CONTACT

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

Locations