Effect of Closed-chain Shoulder Girdle Scapular Depression Exercise on Shoulder Impingement Syndrome
Comparison Between Closed-chain Shoulder Girdle Scapular Depression Exercise and Shoulder Girdle Depression Against Manual Resistance on Patients With Shoulder Impingement Syndrome
1 other identifier
interventional
46
1 country
1
Brief 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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 21, 2022
CompletedFirst Posted
Study publicly available on registry
April 8, 2022
CompletedStudy Start
First participant enrolled
February 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2024
CompletedFebruary 8, 2024
February 1, 2024
29 days
March 21, 2022
February 7, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
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 Outcomes (2)
Range of motion (flexion and abduction) will be measured by Electronic goniometer
20 minutes
Function
30 minutes
Study Arms (2)
Study grou[p
EXPERIMENTALClosed-chain shoulder girdle scapular depression exercise
control group
ACTIVE COMPARATORShoulder girdle depression against manual resistance exercise
Interventions
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- History of cardiac diseases or dyspnea on exertion
- Patients with cervical radiculopathy.
- Patients with shoulder instability.
- Patients with frozen shoulder.
- Acute shoulder trauma.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Nasr Awad Abdelkader Othmanlead
- Atef Abdulalim Nadier, Pharos Universitycollaborator
- Ehab Ai Abdalah,Lecurer, Horus Universitycollaborator
Study Sites (1)
Kafr Elshiekh Hospital
Kafr ash Shaykh, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Assistant Professor,Department of Physical Therapy for Musculoskeletal Disorders
Study Record Dates
First Submitted
March 21, 2022
First Posted
April 8, 2022
Study Start
February 1, 2024
Primary Completion
March 1, 2024
Study Completion
December 1, 2024
Last Updated
February 8, 2024
Record last verified: 2024-02