Scapular Blackburn Stabilization Versus PNF in Impingement Syndrome
impingment
1 other identifier
interventional
51
1 country
1
Brief Summary
purpose of study to Aim to investigate effect(s) of scapular Blackburn stabilization exercises compared toscapular proprioceptive neuromuscular facilitation (SPNF) exercise in addition to conventional exercises on shoulder pain, function, shoulder,sacpular ROM, scapular muscle strength and scapular orientation in patients with sub acromial impingement syndrome Participants will be randomly allocated to three groups as follow: Group A (n=17): will receive a program of conventional exercise include rotator cuff strengthening ,stretching for posterior capsule and stretching for pectoralis minor for 18 sessions (3 sessions per week for six weeks) Group B (n=17): will receive a scapular PNF exercise program in addition to conventional Exercise with the same frequency. Group C (n=17): will receive a scapular Blackburn stabilization exercises in addition to conventional Exercise with the same frequency
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 Jul 2024
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
July 18, 2024
CompletedStudy Start
First participant enrolled
July 30, 2024
CompletedFirst Posted
Study publicly available on registry
August 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 30, 2025
CompletedFebruary 2, 2026
September 1, 2025
11 months
July 18, 2024
January 29, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
shoulder pain and functional disability
Shoulder pain and disability index., minimum number 0=mean No pain and No disabilities and maximum number 10=mean highest pain and maximum disability
Assessment procedure will be performed pre intervention and post third and sixth week of treatment
A-shoulder flexion ROM B- shoulder external rotation C-shoulder internal rotation
Digital Inclinometer.
Assessment procedure will be performed pre intervention and post third and sixth week of treatment
selective muscle strength on: A- upper trapezius B- middle trapezius C-lower trapezius. D- serrates anterior
-Lafayette Hand-held dynamometer
Assessment procedure will be performed pre intervention and post third and sixth week of treatment
scapula orientation
lateral scapular slide test
Assessment procedure will be performed pre intervention and post third and sixth week of treatment
Study Arms (3)
Experimental.
EXPERIMENTALreceive a scapular PNF exercise program in addition to conventional Exercise ,
Experimental
EXPERIMENTALreceive a scapular Blackburn stabilization exercises in addition to conventional Exercise
control group
OTHERExercise only
Interventions
Eligibility Criteria
You may qualify if:
- \. Fifty one Male and female patients with SIS and aged between 30-50.
- \. Body mass index (BMI) 18.5-29.9 kg/m2.
- \. patients complaining primary shoulder impingement.
- \. patients with altered scapular resting positions with scapular dyskinesia with positive lateral scapular slide test.
- patients will be included at least three special tests positive from the following tests:
- A-Hawkins-Kennedy Impingement Test:
- B-Neer"s Impingement Test:
- C- "Empty Can" or Jobe Test D-painful arc test
- E-External rotation resistance test
- F-Cross-body adduction test
- G-Drop arm sign
You may not qualify if:
- Neurological deficit affecting the shoulder function during daily activities.
- Cervical disc pathology.
- Brain injures.
- Fractures in the upper limb
- Undergone shoulder surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
faculty of physical therapy Cairo university
Cairo, Giza Governorate, 022, Egypt
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MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Enas F. Youssef, Prof.Dr
chair person of Department of Physical therapy for Musculoskeletal Disorder and its Surgery
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant lecturer
Study Record Dates
First Submitted
July 18, 2024
First Posted
August 15, 2024
Study Start
July 30, 2024
Primary Completion
June 30, 2025
Study Completion
July 30, 2025
Last Updated
February 2, 2026
Record last verified: 2025-09