Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID06723730

Additional Effects of Mobilization with Movement with Upper Quadrant Core Strengthening in Rotator Cuff Related Pain A Randomized Controlled Trial

Led by Foundation University Islamabad · Updated on 2024-12-09

40

Participants Needed

1

Research Sites

2 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the additional effects of combining mobilization with movement and upper quadrant core strengthening in people experiencing rotator cuff related shoulder pain. This randomized controlled trial aims to determine how these treatments impact pain, range of motion, proprioception, and fear of movement (kinesiophobia). Participants are randomly assigned to one of two groups. One group performs an upper quadrant core strengthening protocol over four weeks, including scapular postural correction, shoulder shrugging, and rotation exercises. The other group performs the same strengthening protocol combined with mobilization techniques involving acromioclavicular, scapular, and glenohumeral joint glides. During the study, participants will have their pain intensity, shoulder range of motion, proprioception, and kinesiophobia measured after four weeks. Data collection includes assessments before and after treatment, and participants provide informed consent before enrollment. The study runs from July 2024 to June 2025.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 65 years
  • Both genders
  • Unilateral shoulder pain caused by injury
  • Numeric pain rating scale less than 8
  • Symptoms lasting more than 6 weeks
  • Pain on active shoulder movement
  • Pain provoked by at least three specific shoulder tests (Neer, Hawkins-Kennedy, Empty Can, Full Can, Painful Arc, Resisted external rotation)
  • Diagnosis by rehabilitation or orthopedic specialist of rotator cuff injury, subacromial impingement syndrome, or subacromial pain
Not Eligible

You will not qualify if you...

  • Complete rotator cuff or biceps brachii rupture
  • Adhesive capsulitis
  • History of shoulder dislocation
  • Glenohumeral osteoarthritis
  • Cancer
  • Auto-immune inflammatory conditions or infection
  • Positive anterior or posterior drawer joint integrity tests
  • Hill-Sachs or Bankart lesions
  • Cervical rib
  • Previous shoulder or neck surgery or fracture
  • Pain caused by neck movements
  • Presence of radicular signs
  • Diagnosis of fibromyalgia
  • Clinical depression
  • Rheumatoid arthritis
  • Poor bone quality (osteoporosis)
  • Vertebrobasilar insufficiency test positive result

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 weeks

Participants perform a four-week upper quadrant core strengthening protocol. Some participants also perform mobilization with movement exercises targeting shoulder joints.

Weekly visits for up to 4 weeks

Trial Site Locations

Total: 1 location

1

Foundation University College of Physical Therapy

Rawalpindi, Punjab Province, Pakistan, 46000

Actively Recruiting

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Research Team

R

Raima Liaqat, MS-MSKPT*

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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