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Scapular Blackburn Stabilization Versus PNF in Impingement Syndrome

NCT06554860 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 51

Last updated 2026-02-02

No results posted yet for this study

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

Conditions

  • Impingement Syndrome

Interventions

OTHER

scapular Blackburn stabilization plus exercise

scapular Blackburn stabilization

OTHER

PNF plus Exercise

PNF plus Exercise

OTHER

exercise only

Exercise only

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Enas F. Youssef, Prof.Dr · chair person of Department of Physical therapy for Musculoskeletal Disorder and its Surgery

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-07-30
Primary Completion
2025-06-30
Completion
2025-07-30

Countries

  • Egypt

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06554860 on ClinicalTrials.gov