ADDITIONAL EFFECTS OF MOBILIZATION WITH MOVEMENT WITH UPPER QUADRANT CORE STRENGTHENING IN ROTATOR CUFF RELATED PAIN:A RANDOMIZED CONTROLLED TRAIL

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorFoundation University Islamabad

About this trial

This study is a randomised control trial and the purpose of this study is to determine the additional effects of mobilization with movement with upper quadrant core strengthening in rotator cuff related pain

.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18-65 years

Both genders

Unilateral shoulder pain of traumatic origin

Scoring should be less than 8 on numeric pain rating scale

Disqualifiers

History and Clinical presentation compatible with complete rotator cuff or bicep brachia rupture

Adhesive capsulitis

History of dislocation

Glenohumeral osteoarthritis

Trial design

Design model

Parallel

Treatments tested in this trial

  • Upper Quadrant Core Strengthening protocol

    Procedure/Surgery

    Upper Quadrant Core Strengthening protocol Core strengthening protocol will comprise of following four week protocol. 1. Week one Scapular postural correction and shoulder shrugging exercises 2. Week two External rotation at 0 degree 3. Week three Internal rotation at 0 degree 4. Week four Standing row at 45 and 90 degree , Anterior shoulder stretch and Thoracic exercise in sitting

  • Mobilization with movement

    Procedure/Surgery

    In addition to upper quadrant core strengthening protocol participants will also perform mobilization with movement. Mobilization with movement protocol will comprise of following forms. 1. Acromioclavicular joint glides 2. Scapular glides 3. Glenohumeral joint glides ( inferior glides, postero-lateral glides, postero-inferior)

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Upper Quadrant Strenghtening + MWM GroupExperimental treatment 2 interventions
Group B: Upper Quadrant Strenghtening GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Pain intensity

Pain will be measured on Numerical Pain rating scale. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable").

Time frame
4 weeks
2

Range of motion

A universal goniometer will be used to measure the shoulder ROM in external \& internal rotation, abduction and flexion and their normal ranges are 90, 80, 0-180, 0-180 degree respectively.

Time frame
4 weeks
3

Proprioception

The laser pointer method for assessing Shoulder Joint Position Sense (JPS) involves the patient using a laser pointer to target a 1 meter distanced scoreboard while performing arm movements. Patient will be asked to perform flexion, abduction and external rotation to 90 degree or alternatively to maximum possible pain free range below 90 degree. After three practice rounds with eyes open, four attempt with eye closed will be performed and shoulder range will be measured. We will measure JPSE for flexion, abduction and external rotation by using mobile app inclinometer.

Time frame
4 weeks
4

Kinesiophobia

The Tampa Scale of Kinesiophobia (TSK) is a 17-item self-report tool with a 4-point Likert scale, measuring fear of movement due to injury or pain, and somatic focus on underlying medical issues. Scores range from 17 to 68, with higher scores (≥37) indicating significant kinesiophobia and poorer health outcomes.

Time frame
4 Weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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