ClinicalTrials.gg
CompletedNCT07229274RCTUpdated Aug 10, 2026Results posted

Effect of Joint Mobilization and Movement Control Exercises on Shoulder Pain and Function in Fast Bowlers (RCT)

An interventional study of Kinetic control for shoulder internal rotation with mobilization with movement and stretches, strengthening and mobilization with movement in Glenohumeral Internal Rotation Deficit (GIRD), sponsored by Lahore University of Biological and Applied Sciences. Completed at 2 sites in Pakistan. Open to male participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-08-10.

Sponsored by Lahore University of Biological and Applied Sciences · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Feb 2025, registered Oct 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Male
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 19 studies in Athletic Injuries with a site in Pakistan — none open to participants now, 1 under way, none of them phase 3. Athletic Injuries · Pakistan.

Enrollment
6th of 19
50 · median 36
Started
2025
with 2 others
No phase
19 of 19
none open now
Registered
19th of 19
by date
Lead sponsor
1 of 19
Lahore University of Biological and Applied Sciences

Among the 19 studies in Athletic Injuries with a site in Pakistan, this one is the 6th largest by enrollment, is one of 3 that started in 2025, is one of 19 with no phase, and was the 19th registered.

Athletic Injuries

258 studies on the registry are indexed under Athletic Injuries; 45 are open to participants now.

Browse Athletic Injuries studies →

Open to participants now

None of the 19 studies in Athletic Injuries with a site in Pakistan is open now.

Who these studies take

Of the 21 Athletic Injuries studies recruiting now, 2 (10%) set no upper age limit and 18 (86%) stop at 75 or younger; 11 take children under 18; 8 take healthy volunteers.

This study: 18 Years to 45 Years · male · no healthy volunteers.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Download CSVNarrow it in search →With an account: the 19 studies in Athletic Injuries with a site in Pakistan as a file.
02

Study summary

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.

03

Conditions studied

  • Glenohumeral Internal Rotation Deficit (GIRD)

Keywords

  • Overhead Athletes
  • Internal Rotation
  • Kinetic Control
  • Sports Injury
  • Musculoskeletal Disorder
04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
50 participants (actual)

Study arms

  • 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

    Other: Kinetic control for shoulder internal rotation with mobilization with movement

  • 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.

    Other: stretches, strengthening and mobilization with movement

Interventions

  • OtherKinetic control for shoulder internal rotation with mobilization with movement

    stretches and strengthening along with mobilization with movement is given to participants. stretches include sleeper stretch and isometrics in strengthening

  • Otherstretches, 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.

06

What researchers measure

Primary outcomes

  1. Pain Intensity

    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.

    Time frame: From enrollment to the end of treatment at 6 weeks

  2. Shoulder Range of Motion

    Shoulder range of motion will be measured in all planes of movement using a universal goniometer. The movements will include: Internal Rotation (0-90°) All measurements will be recorded in degrees to assess improvement in joint mobility across these planes.

    Time frame: From enrollment to the end of treatment at 6 weeks

  3. Functional Disability

    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.

    Time frame: From enrollment to the end of treatment at 6 weeks

07

Results

Posted Aug 10, 2026
Limitations and caveats
Pressure Biofeedback unit wasn't used to stabilize glenohumeral joint movement for any excessive or irrelevant movement

Participant flow

A total of 100 participants initially were assessed for recruitment in which 50 were selected for the final recruitment

Participant flow — Overall Study
MilestoneMovement Control Exercises With the Concept of Kinetic Control and Mobilization With MovementStretches, Strengthening and Mobilization With Movement
Started2525
Completed2525
Not completed00

Outcome measures

PrimaryPain Intensity

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.

Time frame:
From enrollment to the end of treatment at 6 weeks
Reported as:
Mean · Score on scale
Pain Intensity
Score on scaleMovement Control Exercises With the Concept of Kinetic Control and Mobilization With MovementStretches, Strengthening and Mobilization With Movement
Pain Intensity0.96 ± 0.341.36 ± 0.86
PrimaryShoulder Range of Motion

Shoulder range of motion will be measured in all planes of movement using a universal goniometer. The movements will include: Internal Rotation (0-90°) All measurements will be recorded in degrees to assess improvement in joint mobility across these planes.

Time frame:
From enrollment to the end of treatment at 6 weeks
Reported as:
Mean · Degrees
Shoulder Range of Motion
DegreesMovement Control Exercises With the Concept of Kinetic Control and Mobilization With MovementStretches, Strengthening and Mobilization With Movement
Shoulder Range of Motion73.83 ± 6.7267.96 ± 5.72
PrimaryFunctional Disability

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.

Time frame:
From enrollment to the end of treatment at 6 weeks
Reported as:
Mean · Score on Scale
Functional Disability
Score on ScaleMovement Control Exercises With the Concept of Kinetic Control and Mobilization With MovementStretches, Strengthening and Mobilization With Movement
Functional Disability27.76 ± 12.3638.58 ± 9.57

Adverse events

Collected over Adverse events were monitored during the 6-week intervention period. Non-serious events are listed at a 3% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Movement Control Exercises With the Concept of Kinetic Control and Mobilization With Movement0/25 (0%)0/25 (0%)1/25 (4%)
Stretches, Strengthening and Mobilization With Movement0/25 (0%)0/25 (0%)2/25 (8%)
Most frequent other events
Most frequent other events
EventMovement Control Exercises With the Concept of Kinetic Control and Mobilization With MovementStretches, Strengthening and Mobilization With Movement
Pain and Muscle SorenessMusculoskeletal and connective tissue disorders1/252/25

Baseline characteristics

On baseline, 25 participants were recruited in each group with age from 18-45 years

Age, Categorical
Age, Categorical(Participants)Movement Control Exercises With the Concept of Kinetic Control and Mobilization With MovementStretches, Strengthening and Mobilization With MovementTotal
<=18 years8917
Between 18 and 65 years171633
>=65 years000
Sex: Female, Male
Sex: Female, Male(Participants)Movement Control Exercises With the Concept of Kinetic Control and Mobilization With MovementStretches, Strengthening and Mobilization With MovementTotal
Female000
Male252550
Race and Ethnicity Not Collected
Race and Ethnicity Not Collected(Participants)Movement Control Exercises With the Concept of Kinetic Control and Mobilization With MovementStretches, Strengthening and Mobilization With MovementTotal
Count of participants——0
Symptoms Duration
Symptoms Duration(Months)Movement Control Exercises With the Concept of Kinetic Control and Mobilization With MovementStretches, Strengthening and Mobilization With MovementTotal
Mean14.60 ± 2.8613.96 ± 2.7614.32 ± 2.81
Training Time
Training Time(Hours per Week)Movement Control Exercises With the Concept of Kinetic Control and Mobilization With MovementStretches, Strengthening and Mobilization With MovementTotal
Mean9.08 ± 2.0210.2 ± 3.109.64 ± 2.06
08

Study locations

2 sites
  • Sehat Medical Complex
    Lahore, Punjab Province 54000, Pakistan
  • Bata Sports Club
    Lahore, Punjab Province 54850, Pakistan
09

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: Undecided

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Feb 2025 to primary completion in Feb 2026, 12 months.

Results were first posted in Aug 2026, 5 months after primary completion.

Of 119 non-industry interventional studies with no phase under Athletic Injuries, half reached primary completion within 5 months of starting (the median), counting those still running; a quarter within 2 and three quarters within 14. This study's 12 months is above that.

Counting every sponsor, half of 121 studies reached it within 5 months; a quarter within 2 and three quarters within 14.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 2, 2025
First posted
Nov 14, 2025
StartActual
Feb 15, 2025
Primary completionActual
Feb 15, 2026
CompletionActual
Mar 15, 2026
Results first posted
Aug 10, 2026
Last update
Aug 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT07229274
Lead sponsor
Lahore University of Biological and Applied Sciences
Responsible party
Hammad Haider (Dr. Hammad Haider, Masters of Science Student in MSK Physical Therapy, Lahore University of Biological and Applied Sciences) — Principal investigator
First posted
Nov 14, 2025
Start date
Feb 15, 2025
Primary completion
Feb 15, 2026
Completion
Mar 15, 2026
Results posted
Aug 10, 2026
Last update
Aug 10, 2026

Study contacts

Hammad Haider, MS-MSK PT
principal investigator · Lahore University of Biological and Applied Sciences

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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