Effect of High Intensity Exercises in Treatment of Patients With Shoulder Impingement Syndrome

Sponsor

Cairo University (Other)

Overall Status

Recruiting

CT.gov ID

NCT05950880

Collaborator

(none)

Enrollment

Location

Arms

Anticipated Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Purposes of the study

To investigate the effect of adding High-Intensity Exercises to conventional physical therapy in patients with Shoulder Impingement Syndrome

Condition or Disease	Intervention/Treatment	Phase
Shoulder Impingement Syndrome	Other: High intensity shoulder exercise Other: Conventional physical therapy	N/A

Detailed Description

Patients will be randomized into either High-intensity shoulder exercise group or Conventional physical therapy group. Patients will receive the intervention for six weeks. Outcomes will be assessed at baseline and post-intervention.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

32 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Double (Participant, Outcomes Assessor)

Primary Purpose:

Treatment

Official Title:

Effect of Adding High Intensity Exercises to Conventional Physical Therapy in Treatment of Athlete Patients With Shoulder Impingement Syndrome

Actual Study Start Date :

Jan 1, 2023

Anticipated Primary Completion Date :

Sep 1, 2023

Anticipated Study Completion Date :

Sep 1, 2023

Arms and Interventions

Arm	Intervention/Treatment
Experimental: High intensity exercise + Conventional physical therapy Patients in this group will receive High-intensity exercise + Conventional physical therapy	Other: High intensity shoulder exercise Exercises that target the rotator cuff muscles using 90% of one repetition maximum only for 5 repetitions Other: Conventional physical therapy Conventional physical therapy consisting of scapular stabilization exercises, posterior capsule stretch, and rotator cuff activation exercises
Active Comparator: Conventional physical therapy Patients in this group will receive Conventional physical therapy	Other: Conventional physical therapy Conventional physical therapy consisting of scapular stabilization exercises, posterior capsule stretch, and rotator cuff activation exercises

Arm

Intervention/Treatment

Experimental: High intensity exercise + Conventional physical therapy

Patients in this group will receive High-intensity exercise + Conventional physical therapy

Other: High intensity shoulder exercise

Exercises that target the rotator cuff muscles using 90% of one repetition maximum only for 5 repetitions

Other: Conventional physical therapy

Conventional physical therapy consisting of scapular stabilization exercises, posterior capsule stretch, and rotator cuff activation exercises

Active Comparator: Conventional physical therapy

Patients in this group will receive Conventional physical therapy

Other: Conventional physical therapy

Conventional physical therapy consisting of scapular stabilization exercises, posterior capsule stretch, and rotator cuff activation exercises

Outcome Measures

Primary Outcome Measures

pain and function [Change from Baseline pain and function at 6 weaks]
Shoulder pain and disability index (SPADI)
Supraspinatus muscle thickness [Change from Baseline Supraspinatus muscle thickness at 6 weaks]
Diagnostic Ultrasound

Secondary Outcome Measures

Sub acromial space (Acromiohumeral distance). [Change from Baseline Sub acromial space at 6 weaks]
Diagnostic Ultrasound
External and internal rotators muscle strength. [Change from Baseline External and internal rotators muscle strength at 6 weaks]
Hand-held dynamometer
supuraspinatus muscle strength [Change from Baseline supuraspinatus muscle strength at 6 weaks]
Hand-held dynamometer
shoulder performance [Change from Baseline shoulder performance at 6 weaks]
Timed push up test

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 35 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Athletic patients
Age of the patients between 18 - 35 years
Unilateral shoulder pain more than 3 months.
Positive Hawkins test.
Positive empty or full cane test.
Pain at night or incapable of lying on the shoulder.
Pain with active shoulder elevation in the scapular plane.
History of pain in the C5-C6 dermatome.
Pain with palpation of the rotator cuff tendons.
The patient had pain with resisted isometric abduction

Exclusion Criteria:

History of shoulder instability (positive Sulcus sign, positive apprehension test, and history of shoulder dislocation).
Clinical sign of cervical radiculopathy.
History of acromio -clavicular pain.
Rheumatoid Arthritis.
Adhesive capsulitis.
Tumors
Labrum lesions
Capsular or ligamentous tears or avulsions
Cartilage lesions

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	facult of physical therapy,MTI	Cairo		Egypt

Sponsors and Collaborators

Cairo University

Investigators

Principal Investigator: Abdallah Gamiel, MSc, Cairo University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Abdallah Gamiel Ayed, Mr, Cairo University

ClinicalTrials.gov Identifier:

NCT05950880

Other Study ID Numbers:

P.T.REC/012/004361

First Posted:

Jul 18, 2023

Last Update Posted:

Jul 18, 2023

Last Verified:

Jul 1, 2023

Individual Participant Data (IPD) Sharing Statement:

Plan to Share IPD:

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

Shoulder Impingement Syndrome

Syndrome

Rotator Cuff Injuries

Study Results

No Results Posted as of Jul 18, 2023