- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06845189
Role of Modified Robbery Exercises on Scapular Dyskinesis in Frozen Shoulder
Role of Modified Robbery Exercises on Scapular Dyskinesis in Patients With Frozen Shoulder
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54810
- School of Allied Health Sciences, CMH Lahore Medical College & Institute of Dentistry
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Collaborators
Investigators
- Principal Investigator: Wajida Perveen, School of Allied Health Sciences, CMH Lahore Medical College & IOD (NUMS Rawalpindi)
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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