NCT06554860

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
51

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 18, 2024

Completed
12 days until next milestone

Study Start

First participant enrolled

July 30, 2024

Completed
16 days until next milestone

First Posted

Study publicly available on registry

August 15, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2025

Completed
Last Updated

February 2, 2026

Status Verified

September 1, 2025

Enrollment Period

11 months

First QC Date

July 18, 2024

Last Update Submit

January 29, 2026

Conditions

Keywords

Scapular Blackburn stabilizationScapular PNF

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.

EXPERIMENTAL

receive a scapular PNF exercise program in addition to conventional Exercise ,

Other: scapular Blackburn stabilization plus exercise

Experimental

EXPERIMENTAL

receive a scapular Blackburn stabilization exercises in addition to conventional Exercise

Other: PNF plus Exercise

control group

OTHER

Exercise only

Other: exercise only

Interventions

PNF plus Exercise

Experimental

Exercise only

control group

scapular Blackburn stabilization

Experimental.

Eligibility Criteria

Age30 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Study Sites (1)

faculty of physical therapy Cairo university

Cairo, Giza Governorate, 022, Egypt

Location

Related Publications (79)

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MeSH Terms

Interventions

Exercise

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Enas F. Youssef, Prof.Dr

    chair person of Department of Physical therapy for Musculoskeletal Disorder and its Surgery

    PRINCIPAL INVESTIGATOR

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

Locations