Role of Modified Robbery Exercises on Scapular Dyskinesis in Frozen Shoulder

February 7, 2026 updated by: Wajida Perveen, CMH Lahore Medical College and Institute of Dentistry

Role of Modified Robbery Exercises on Scapular Dyskinesis in Patients With Frozen Shoulder

The study aims to find out the role of the modified robbery exercises in the management of scapular dyskinesia in patients with frozen shoulders. This single-blind randomized clinical study will be conducted at approved study center in Lahore Pakistan in line with the ethical principles stated in Declaration of Helsinki. Pain, muscle Activation, ROM, scapular dyskinesia, muscle strength, functional limitation and participants' wellbeing will be recorded at baseline, after week three, and after week six in both intervention and control groups.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

Scapular Dyskinesia is regarded as the altered scapular kinematics, presenting with increased scapular upward rotation and eminence of the medial border in patients with shoulder injuries. Patients with frozen shoulder present with a certain degree of scapular dyskinesia. The objective of the study is to find out the role of the modified robbery exercises in the management of scapular dyskinesia in patients with frozen shoulders. This single-blind randomized clinical study will be conducted at approved study center in Lahore Pakistan. The study will abide by the ethical principles in line with the Declaration of Helsinki. Baseline data of the participants of pain, muscle Activation, ROM, scapular dyskinesia, muscle strength, functional limitation and participants' wellbeing will be recorded. Group A will receive the modified robbery exercises three days a week for six weeks, group B will receive the conventional physical therapy protocol three days a week for six weeks. Outcomes will be assessed at baseline, after week three, and after week six.

Data will be recorded using questionnaires, proforma and the other listed outcome measurement tools. on the base of normality of the data appropriate parametric test or non-parametric test will be applied for intra and inter group comparison.

Study Type

Interventional

Enrollment (Estimated)

63

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

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 54810
        • School of Allied Health Sciences, CMH Lahore Medical College & Institute of Dentistry

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

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Patients of both genders
  • Patients of age 35 to 55 years
  • Modified Lateral Scapular Slide Test score > 1.4 cm
  • Pain on VAS ≥4 out of 10.
  • Pain in the shoulder for at least 3 months
  • Diagnosed unilateral frozen shoulder
  • Limited Scapular upward rotation, Capsular pattern (more limited external rotation than abduction),
  • Scapular dispositioning and visible Inferior medial border prominence.

Exclusion Criteria:

  • Patients with frozen shoulders having less than 90 degrees of flexion and abduction.
  • Participants with cervical radicular pain
  • Pregnant females
  • Presence of red flags to the treatment
  • History of recent trauma to the spine or the shoulder complex.
  • History of recent shoulder surgery
  • Any neurological deficit i.e winged scapula
  • Other pathologies like cervical myelopathy and prolapsed cervical disc.
  • Known cases of neurological, radiculopathy, and inflammatory diseases.
  • Having spinal deformities such as scoliosis or kyphosis.
  • Vestibular or respiratory disorder, Auditory or cognitive impairment
  • Taking medication that may affect the balance and coordination.

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Modified Robbery Exercises Group
the participants will receive prescribed set of Modified Robbery exercises
Prescribed set of Modified Robbery exercises will be applied
Active Comparator: Conventional Physiotherapy treatment
the participants will receive conventional physiotherapy treatment for Frozen shoulder.
Conventional Physiotherapy Treatment for Frozen Shoulder

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain intensity
Time Frame: baseline, at week 3 and at week 6
Pain intensity will be measured using Visual Analogue Scale.
baseline, at week 3 and at week 6
Scapular Dyskinesia
Time Frame: baseline, at week 3 and at week 6
Score of Modified Lateral Scapular Slide Test using Vernier caliper
baseline, at week 3 and at week 6
Range of scapular and shoulder Motion
Time Frame: baseline, at week 3 and at week 6
Range of Motion of selected movements will be measured on Goniometer
baseline, at week 3 and at week 6
Muscle Strength
Time Frame: baseline, at week 3 and at week 6
Muscle Strength of selected muscles will be measured by manual muscle testing
baseline, at week 3 and at week 6
Muscle activation
Time Frame: baseline, at week 3 and at week 6
Muscle activation of selected muscles will be measured by Electromyography Biofeedback
baseline, at week 3 and at week 6

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
shoulder functions
Time Frame: baseline, at week 3 and at week 6
shoulder functions will be assessed using Shoulder pain and disability Index (SPADI-U)
baseline, at week 3 and at week 6
Well-being
Time Frame: baseline, at week 3 and at week 6
Well-being of the participants will be assessed using the WHO 5 Wellbeing Index
baseline, at week 3 and at week 6

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Wajida Perveen, School of Allied Health Sciences, CMH Lahore Medical College & IOD (NUMS Rawalpindi)

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)

February 26, 2025

Primary Completion (Actual)

January 25, 2026

Study Completion (Estimated)

August 25, 2026

Study Registration Dates

First Submitted

February 20, 2025

First Submitted That Met QC Criteria

February 20, 2025

First Posted (Actual)

February 25, 2025

Study Record Updates

Last Update Posted (Actual)

February 10, 2026

Last Update Submitted That Met QC Criteria

February 7, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 109/ERC/CMH/LMC

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.

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