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Range of MotionNCT06947239

Additional Effects of Mirror Therapy on Shoulder Mobility and Function in Post-stroke Adhesive Capsulitis Patients

A study testing Mirror therapy along with conventional therapy in people with Range of Motion and Adhesive Capsulitis, run by Foundation University Islamabad at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The estimated annual incidence of stroke in Pakistan is 250/100, 000. Upper limb impairments and post-stroke musculoskeletal complications such as pain, subluxation and restricted joint range of motion are commonly reported. Read more about this study

Who is it for?
Ages 40 to 70 years
What is being tested?
Mirror therapy along with conventional therapy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
22 participants
Where
1 sitePakistan
Study dates
20 Jun 2024to 20 Jan 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Both genders male and female
  • Age 40-70 years
  • Ability to understand and follow simple verbal instructions
  • Patients able to stand for at least 10-15 mins.
  • Ability to participate in a therapy session by coming to hospital.
  • Chronic Stroke (ischemic) patients (6 months-1year) with adhesive capsulitis (capsular pattern :external rotation> abduction > internal rotation)
  • Scores of >24 on Montreal Cognitive assessment scale.

Who cannot join

  • Upper limb fractures or cervical spine pathology or radiculopathy
  • History of upper limb surgery or trauma
  • Rotator cuff pathology or prolonged immobilization of upper limb
  • Rheumatic disease, fibromyalgia or any other musculoskeletal disorder that is altering upper extremity movement
  • Any other neurological condition

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Foundation University College of Physical Therapy

    Islamabad, 44000

Other trials in Pakistan

About this study

The estimated annual incidence of stroke in Pakistan is 250/100, 000. Upper limb impairments and post-stroke musculoskeletal complications such as pain, subluxation and restricted joint range of motion are commonly reported. Among many other shoulder impairments, adhesive capsulitis is a leading cause of limited mobility, reduced range of motion, and pain in stroke patients.

The aim of the current study will benefit the clinicians and physiotherapists as it provide an insight to treat post stroke adhesive capsulitis. Effects of mirror therapy have been established but the literature does not provide best treatment approaches or modalities for different types of Hemiplegic shoulder pain. This study will address the limitations in treatment approaches concerning the shoulder joint and its mobility in post-stroke adhesive capsulitis.

Read more

The study will be non-blinded randomized control trial, consisting of two groups. Study will be conducted over a period of 1 year. Subjects will be selected via non-probability purposive sampling technique using coin toss method followed by randomization into two groups (A and B).Ethical approval will be obtained from ERC FUMC.

One group will receive mirror therapy while other will receive conventional exercises treatment for period of 6 weeks. Baseline tests will be performed before and after the intervention of mirror therapy \& outcome measure assessments will be done after every 3 weeks for a total period of 6 weeks intervention period. Data will be entered and analyzed on SPSS version 22.

Read the detailed description

OBJECTIVES OF STUDY

  1. To determine the effects of mirror therapy along with conventional therapy on improving shoulder joint range of motion in post-stroke adhesive capsulitis patients.
  2. To determine the effects of mirror therapy along with conventional therapy on improving shoulder joint function in post-stroke adhesive capsulitis patients.
  3. To compare the difference between the effects of mirror therapy with conventional therapy alone for improving shoulder mobility and function in post stroke adhesive capsulitis patients.

HYPOTHESIS ALTERNATE HYPOTHESIS

  1. There is a statistically significant effect of mirror therapy in improving the shoulder joint Range Of Motion in post-stroke adhesive capsulitis patients. (p > 0.05).
  2. There is a statistically significant effect of mirror therapy in improving the shoulder joint function in post-stroke adhesive capsulitis patients. (p > 0.05).

NULL HYPOTHESIS

  1. There is a statistically significant effect of mirror therapy in improving the shoulder joint Range Of Motion in post-stroke adhesive capsulitis patients. (p > 0.05).
  2. There is a statistically significant effect of mirror therapy in improving the shoulder joint function in post-stroke adhesive capsulitis patients. (p > 0.05).
Being tested
Mirror therapy along with conventional therapy, Control Group
Keywords
post stroke patients, Range of motion correction, mirror therapy exercises
Medical subject headings
Bursitis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Mirror therapy along with conventional therapyProcedure or surgery

    The experimental group will receive 20 minutes of conventional therapy followed by 20 minutes of mirror therapy training including 3 minutes of rest period between the interventions.

    WEEK OF INTERVENTION:

    TASK PERFORM IN FRONT OF MIRROR:

    WEEK :1-2

    ACTIVE SHOULDER ROM:

    flexion, abduction, external-internal rotation movements of the intact extremity

    Increase the number of repetition according to the patient progression

    WEEK:3-4

    ACTIVITIES TARGETING SHOULDER ROM:

    Cleaning the mirror with a towel(internal rotation+ abduction)

    Lifting a glass to drink ( flexion + abduction)

    Holding a brush to comb hair (external rotation

    WEEK:5-6

    Overhead reaching

    (pasting stickers on the

    mirror)(internal rotation

    / abduction)

    Lifting a bottle overhead.

    ( flexion/abduction)

    Throwing a ball (external

    rotation)

    PROGRESSION OF TASK SPECIFIC MIRROR THERAPY:

    WEEK: 1-2 Increase the number of repetition according to the patient progression WEEK:3-4 Add water in glass Transfer glass

  • Control GroupProcedure or surgery

    Details: Weeks wise:

    The control group will receive 20 mints of conventional therapy .

    1. Heat pack \& TENS to alleviate pain for 15 minutes
    2. Shoulder isometric exercises 10 reps
    3. Active and passive Range of Motion exercises 10 reps each
    4. Codman exercises 10 reps each
    5. Wand exercises 10 reps each
Study groups in NCT06947239
Study groupRoleWhat they receive
Mirror therapy along with conventional therapyExperimentalIt includes participants receiving mirror therapy session in adhesive capsulitis of post stroke patients for a period of 6 weeks. The experimental group will receive 20 minutes of conventional therapy followed by 20 minutes of mirror therapy training including 3 minutes of rest period between the interventions.
Receives: Procedure: Mirror therapy along with conventional therapy
Conventional TherapyActive comparatorit includes 11 participants receiving conventional physical therapy for a period of 6 weeks. The control group will receive the conventional therapy for 40 minutes including: 1. Heat pack \& TENS to alleviate pain for 15 minutes 2. Shoulder isometric exercises 10 reps
Receives: Procedure: Control Group

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Range of motion

    Goniometer will be used to assess range of motion at the shoulder

    Measured: 6 weeks

  2. cognitive impairment

    Montreal cognitive assessment test that was used to detect mild cognitive impairment

    Measured: 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Apr 2025
  2. Study start20 Jun 2024
  3. Primary completion20 Dec 2024
  4. Study completion20 Jan 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
22 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06947239
Sponsor's protocol ID
FUI/CTR/2024/67
Status last verified
Apr 2025
First submitted
21 Apr 2025
Last updated
27 Apr 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Mirror therapy along with conventional therapy in people with Range of Motion and Adhesive Capsulitis, run by Foundation University Islamabad at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Range of motion (time frame: 6 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Apr 2025.

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