- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07229274
Effect of Joint Mobilization and Movement Control Exercises on Shoulder Pain and Function in Fast Bowlers (RCT) (RCT)
Combined Effects of Mulligan Mobilization With Movement and Kinetic Medial Rotation Control for Shoulder on Pain, Range of Motion, and Function Among Fast Bowlers
The goal of this clinical trial is to determine combined effects of the Kinetic control for shoulder on pain, range, and function among fast bowlers. The main question it aims to answer is:
Does mulligan mobilization with movement along with kinetic medial rotation control work in decreasing pain, improving shoulder internal range of motion and shoulder function in fast bowlers with glenohumeral internal rotation deficit? Is the combination of Mulligan mobilization with movement along with kinetic control therapy effective in fast bowlers with glenohumeral internal rotation deficit? Treatment arm will receive movement retraining exercises to develop kinetic control with mulligan mobilization and comparison arm will receive standard physical therapy exercises with mulligan mobilization.
Treatment group will receive shoulder warm up exercises, movement retraining exercises and mulligan mobilization with movement.
Comparison group will receive shoulder warm up exercises, modified sleeper stretch, shoulder isometrics and mulligan mobilization with movement.
Study Overview
Status
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab Province
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Lahore, Punjab Province, Pakistan, 54000
- Sehat Medical Complex
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Lahore, Punjab Province, Pakistan, 54850
- Bata Sports Club
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male cricketers aged 18-45 years.
- Participants experiencing persistent mild to moderate shoulder pain during overhead movements for more than 3 months.
- Fast bowlers actively participating in regular cricket training sessions.
- Presence of Glenohumeral Internal Rotation Deficit (GIRD) greater than 10 degrees, measured with a goniometer by comparing internal rotation of the dominant and non-dominant shoulders.
Exclusion Criteria
- Cricketers who have undergone shoulder (e.g., rotator cuff repair, arthroscopic labrum repair) or elbow surgery within the past 3 months.
- Participants presenting with numbness or tingling sensations in the upper extremity.
- Individuals with comorbidities such as a history of cardiac or pulmonary diseases.
- Subjects with a history of recurrent shoulder dislocations or shoulder instability.
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: Movement control exercises with the concept of kinetic control and mobilization with movement
Each person will follow this program three times a week. The session starts with a shoulder movement test to check how well the shoulder rotates-60 degrees inward and 45 degrees outward-without the shoulder blade or upper arm moving incorrectly. Next, movement retraining exercises are used to fix any incorrect shoulder movements. This includes helping the shoulder and shoulder blade move properly using hands-on support, along with exercises that may be supported or unsupported. Visual cues (like mirrors), touch, and manual guidance are used to teach correct movement. Lastly, Mobilization with Movement (MWM) is performed. This involves gently pushing the shoulder joint backward |
stretches and strengthening along with mobilization with movement is given to participants.
stretches include sleeper stretch and isometrics in strengthening
|
|
Active Comparator: Stretches, strengthening and mobilization with movement
Each person in the control group will do these exercises three times a week. The session starts with shoulder warm-up exercises like arm circles, shoulder rolls, and reaching overhead. These are done in 2 sets of 10 reps. Next is the modified sleeper stretch. This is repeated 3 times, with a 30-second rest between each stretch. Then, isometric shoulder exercises are done in standing. The person pushes their arm inward against resistance without actually moving it. Finally, Mobilization with Movement (MWM) is used. |
Each person in the control group will do these exercises three times a week.
The session starts with shoulder warm-up exercises like arm circles, shoulder rolls, and reaching overhead.
These are done in 2 sets of 10 reps.
Next is the modified sleeper stretch.
This is repeated 3 times, with a 30-second rest between each stretch.
Then, isometric shoulder exercises are done in standing.
The person pushes their arm inward against resistance without actually moving it.
Finally, Mobilization with Movement (MWM) is used.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain intensity
Time Frame: baseline, 3 weeks and 6 weeks
|
Pain intensity will be evaluated using the Numeric Pain Rating Scale (NPRS) ranging from 0 to 10, where 0 indicates no pain, 1-3 represents mild pain, 4-6 indicates moderate pain, and 7-10 reflects severe pain.
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baseline, 3 weeks and 6 weeks
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Shoulder Range of Motion
Time Frame: All outcomes will be recorded at baseline, after 3 weeks, and after 6 weeks of intervention.
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Shoulder range of motion will be measured in all planes of movement using a universal goniometer. The movements will include: Flexion (0-180°) Extension (0-60°) Abduction (0-180°) Adduction (0-40°) Internal Rotation (0-70°) External Rotation (0-90°) All measurements will be recorded in degrees to assess improvement in joint mobility across these planes. |
All outcomes will be recorded at baseline, after 3 weeks, and after 6 weeks of intervention.
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Functional disability
Time Frame: All outcomes will be recorded at baseline, after 3 weeks, and after 6 weeks of intervention.
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Functional disability will be assessed using the Shoulder Pain and Disability Index (SPADI), which provides a percentage score ranging from 0 to 100%.
A low score (0-29%) represents minimal disability, a moderate score (30-59%) indicates moderate disability, and a high score (60-100%) signifies severe functional limitation.
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All outcomes will be recorded at baseline, after 3 weeks, and after 6 weeks of intervention.
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Collaborators and Investigators
Investigators
- Principal Investigator: Hammad Haider, MS-MSK PT, Lahore University of Biological and Applied Sciences
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UBAS/ERB/FoRS/25/022
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
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