NCT06944756

Brief Summary

Shoulder pain is an experience that most of the people can expect to deal in their lives due to over-exertion or postural asymmetries, which may or may not have it interfering with the normal activities of their daily living. Shoulder pain associated with scapular dyskinesia can be associated with restricted joint range of motion and loss of muscle strength, and is among the most common conditions treated by physical therapists. The patho-mechanisms of shoulder pain are only scarcely known but it is associated with both psychosocial and physical factors. Although there is some evidence of pain reduction, improving range of motion and function occurring following global posture reeducation, scapular stabilizing exercise, it is not known how the training influences the muscle activities of persons shoulder pain associated scapular dyskinesia.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2019

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 6, 2019

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 6, 2019

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 10, 2019

Completed
5.5 years until next milestone

First Submitted

Initial submission to the registry

April 7, 2025

Completed
18 days until next milestone

First Posted

Study publicly available on registry

April 25, 2025

Completed
Last Updated

April 25, 2025

Status Verified

April 1, 2025

Enrollment Period

3 months

First QC Date

April 7, 2025

Last Update Submit

April 17, 2025

Conditions

Keywords

Scapular DyskinesiaShoulder PainGlobal Posture Reeducation

Outcome Measures

Primary Outcomes (5)

  • Shoulder Flexion Range of Motion

    Goniometer

    Pre, 3rd week, 5th week

  • Shoulder Abduction ROM

    Goniometer

    Pre, 3rd week, 5th week measured using degree of movement (160 to 180)

  • Shoulder Pain

    Numeric Pain Rating Scale

    Pre, 3rd week, 5th week (Score measuring on on a scale of 0 to 10, 0 being no Pain and 10 being worst)

  • Shoulder Disability

    Disability of arm shoulder and hand

    Pre, 3rd week, 5th week (scoring 0-100, 0 being no disability and 100 being most sever disability)

  • Shoulder Function

    Pennsylvania Shoulder scale

    Pre, 3rd week, 5th week (scoring 0-100, 0 being poor shoulder function and 100 being most best shoulder fucntions)

Study Arms (2)

GROUP A: GPR

EXPERIMENTAL

Two stretching postures were maintained for 10 minutes each.

Other: Global Postural Reeducation

GROUP B: SSE

EXPERIMENTAL

1\) Push up plus and 2) press up, were selected in reference to a study for scapular stabilization.

Other: Scapular Stabilization Exercises

Interventions

Two stretching postures were maintained for 10 minutes each. * In order to stretch the posterior muscle chain(the supine posture with hip flexion, which stretches the posterior muscle chain) the patient lay in the supine position with the occipital, lumbar, and sacral spine stabilized, with the lower limbs at 90° hip flexion, and performed gradual knee extensions, and dorsiflexion of the ankle. * In order to stretch the anterior muscle chain (the supine posture with leg extension, which progressively stretches the anterior muscle chain) the patient lay in the supine position with the upper limbs abducted at 30° and the forearms supine.. Hips were flexed, abducted, and laterally rotated, with the soles of the feet touching each other. Gradually, respecting the patient's limits, the lower limbs were extended as much as possible and adduction of the upper limbs.

GROUP A: GPR

1\) Push up plus and 2) press up, were selected in reference to a study for scapular stabilization. During the 5-week intervention training, sets of repetitions were increased progressively. In the first week participants performed 3 sets of each exercise (10 repetitions × 10-second duration each) and worked up to a maximum of 5 sets of 10 repetitions in the last weeks of the intervention.

GROUP B: SSE

Eligibility Criteria

Age20 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patients of both genders.
  • SD of type I with scapular malposition, inferior medial border prominence, coracoid pain and malposition, and dyskinesia of scapular movement (SICK) Scapula Rating Scale, in association to shoulder pain (pain for at least 3 months).
  • Pain intensity ranges from 2-9 on scale of shoulder in last month.

You may not qualify if:

  • Additional cervical or shoulder pathology (cervical stenosis, myelopathy, prolapsed intervertebral disk )
  • Pre-diagnosed winged scapula due to lesions of the long thoracic nerve or spinal accessory nerve.
  • Patients with shoulder instability
  • Medical red flag history (tumor, metabolic diseases, rheumatoid arthritis, osteoporosis or Infection)
  • Any Neurological disorder that affects shoulder
  • History of Severe trauma or any fracture of shoulder girdle
  • Hypertension (Systolic BP\[160, diastolic BP\[100\])
  • Cardiovascular diseases (e.g., chest pain during physical exercise, heart failure, myocardial infarction)
  • Postoperative conditions in the neck and affected shoulder region Pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ali Hospital

Lahore, Punjab Province, 54000, Pakistan

Location

MeSH Terms

Conditions

Shoulder Pain

Condition Hierarchy (Ancestors)

ArthralgiaJoint DiseasesMusculoskeletal DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Aiza Yousaf, DPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
Patients and assessor blinded
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: RCT
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 7, 2025

First Posted

April 25, 2025

Study Start

April 6, 2019

Primary Completion

July 6, 2019

Study Completion

October 10, 2019

Last Updated

April 25, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

Locations