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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05318209
Other study ID # P.T.REC/012/003377
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 1, 2024
Est. completion date December 1, 2024

Study information

Verified date February 2024
Source Cairo University
Contact Nasr A. Abdelkader, PhD
Phone 00201025771117
Email dr.nasrawad@cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

forty patients will be assigned randomly into 2 equal groups Study group (n=23) will receive "closed-chain shoulder girdle scapular depression exercise" in addition to Stretching for posterior capsule & pectoralis minor, Eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound Control group B (n=23) will receive "shoulder girdle depression against manual resistance exercise" in addition to stretching for posterior capsule & pectoralis minor, eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound . The exercise program will consist of 3 sessions / week for 5 weeks


Description:

BACKGROUND: Patients with shoulder impingment syndrome report disability, especially during overhead movements, which may hinder activities of daily living . Muscular strengthening training influences the resting position and scapular movement pattern of subjects with shoulder impingement syndrome and improve function of the affected shoulder. Therefore, the focus of treatment for the syndrome is on performing exercises, including stretching, strengthening, and neuromuscular control exercises. Although multiple types of exercise, such as scapular stability exercises, strengthening of the rotator cuff through range, and flexibility exercises for the anterior and posterior shoulder exercise is effective in the management of patients with shoulder impingement syndrome, there is not enough evidence to say whether one mode of exercise is superior to another. RESEARCH QUESTION: Are there any difference between closed-chain shoulder girdle scapular depression exercise and shoulder girdle depression against manual resistance exercise on patients with shoulder impingement syndrome METHODS: forty patients will be assigned randomly into 2 equal groups Study group (n=23) will receive "closed-chain shoulder girdle scapular depression exercise" in addition to Stretching for posterior capsule & pectoralis minor, Eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound Control group B (n=23) will receive "shoulder girdle depression against manual resistance exercise" in addition to stretching for posterior capsule & pectoralis minor, eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound . The exercise program will consist of 3 sessions / week for 5 weeks


Recruitment information / eligibility

Status Recruiting
Enrollment 46
Est. completion date December 1, 2024
Est. primary completion date March 1, 2024
Accepts healthy volunteers No
Gender All
Age group 25 Years to 45 Years
Eligibility Inclusion Criteria: - Patients aged from 25 to 45 years old. - Patients with shoulder impingement stage I &II as judged by criteria of neer classification. - Patients diagnosed by orthopedic surgeon with shoulder impingement, the diagnosis will be confirmed by positive Neer and Hawkins tests. Exclusion Criteria: - History of cardiac diseases or dyspnea on exertion - Patients with cervical radiculopathy. - Patients with shoulder instability. - Patients with frozen shoulder. - Acute shoulder trauma.

Study Design


Intervention

Other:
Exercise
Closed-chain Shoulder Girdle Scapular Depression Exercise

Locations

Country Name City State
Egypt Kafr Elshiekh Hospital Kafr Ash Shaykh

Sponsors (3)

Lead Sponsor Collaborator
Nasr Awad Abdelkader Othman Atef Abdulalim Nadier, Pharos University, Ehab Ai Abdalah,Lecurer, Horus University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain will be measured by visual analogue scale 10cm visual analogue scale (0= no pain, and 10= maximum pain) will be used to determine overall shoulder pain 10 minutes
Secondary Range of motion (flexion and abduction) will be measured by Electronic goniometer Electronic Goniometer will be used to measure shoulder range of motion (Flexion and abduction) 20 minutes
Secondary Function shoulder function will be measured by western Ontario Rotator Cuff Questionnaire (WORC). 30 minutes
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