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Impingement SyndromeimpingmentNCT06554860

Scapular Blackburn Stabilization Versus PNF in Impingement Syndrome

A study testing scapular Blackburn stabilization plus exercise, PNF plus Exercise and exercise only in people with Impingement Syndrome, run by Cairo University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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… Read more about this study

Who is it for?
Ages 30 to 50 years
Conditions the study is for
Impingement Syndrome
What is being tested?
scapular Blackburn stabilization plus exercise, PNF plus Exercise and exercise only
Could I receive a placebo?
No, everyone receives an active treatment
How many people
51 participants
Where
1 siteEgypt
Study dates
30 Jul 2024to 30 Jul 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 30 to 50 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 1. Fifty one Male and female patients with SIS and aged between 30-50.
  • 2. Body mass index (BMI) 18.5-29.9 kg/m2.
  • 3. patients complaining primary shoulder impingement.
  • 4. patients with altered scapular resting positions with scapular dyskinesia with positive lateral scapular slide test.
  • 5- patients will be included at least three special tests positive from the following tests:
  • A-Hawkins-Kennedy Impingement Test:
Show all 11Show fewer
  • 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

Who cannot join

  • 1- Neurological deficit affecting the shoulder function during daily activities.
  • 2-Cervical disc pathology.
  • 3- Brain injures.
  • 4- Fractures in the upper limb
  • 5-Undergone shoulder surgery

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • faculty of physical therapy Cairo university

    Cairo, Giza Governorate, 022

Other trials in Egypt

About this study

Official title: Scapular Blackburn Stabilization Versus Proprioceptive Neuromuscular Facilitation in Subacromial Impingement Syndrome

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

Read the detailed description

Sub-acromial impingement syndrome(SIS) is the most frequent cause of pain and overhead reach limitation in the shoulder area. It occurs when there is impingement of tendons or bursa in the shoulder from bones of the shoulder. Intrinsic and extrinsic factors that contribute to the development of SIS include inflammation in the supra humeral space, inhibition of the rotator cuff muscles, degeneration of the rotator cuff tendons, abnormal scapular position and kinematics. Currently SIS covers a range of pathologies from sub acromial bursitis to rotator cuff tendinopathy and full thickness rotator cuff tears.

The trial will guide physical therapists in selecting effective therapeutic interventions for patients with SAIS and scapular dyskinesia, aiming to reduce the number of treatment sessions, speed up recovery, and improve shoulder pain and functional abilities.

Scapular Blackburn stabilization exercise minimizes excessive superior translation of the humeral head in the glenoid fossa during elevation and subacromial space impingement, consequently addressing shoulder impingement. It also strengthens the scapulothoracic and rotator cuff muscles and decreases muscle imbalance.

Proprioceptive Neuromuscular Facilitation has been described as a comprehensive rehabilitation concept, promoting motor learning, motor control, strength and mobility.

This comprehensive rehabilitation approach includes task-oriented training with manual facilitation aimed at motor learning and motor control.

therefore, what are the effects of scapular Blackburn stabilization and PNF techniques in addition to conventional exercises on shoulder pain, function, shoulder ROM, scapular muscle strength, and scapular orientation in patients with sub acromial impingement syndrome?

Being tested
scapular Blackburn stabilization plus exercise, PNF plus Exercise, exercise only
Keywords
Scapular Blackburn stabilization, Scapular PNF

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • scapular Blackburn stabilization plus exerciseOther

    scapular Blackburn stabilization

  • PNF plus ExerciseOther

    PNF plus Exercise

  • exercise onlyOther

    Exercise only

Study groups in NCT06554860
Study groupRoleWhat they receive
Experimental.Experimentalreceive a scapular PNF exercise program in addition to conventional Exercise ,
Receives: Other: scapular Blackburn stabilization plus exercise
ExperimentalExperimentalreceive a scapular Blackburn stabilization exercises in addition to conventional Exercise
Receives: Other: PNF plus Exercise
control groupOtherExercise only
Receives: Other: exercise only

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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

    Measured: Assessment procedure will be performed pre intervention and post third and sixth week of treatment

  2. A-shoulder flexion ROM B- shoulder external rotation C-shoulder internal rotation

    Digital Inclinometer.

    Measured: Assessment procedure will be performed pre intervention and post third and sixth week of treatment

  3. selective muscle strength on: A- upper trapezius B- middle trapezius C-lower trapezius. D- serrates anterior

    -Lafayette Hand-held dynamometer

    Measured: Assessment procedure will be performed pre intervention and post third and sixth week of treatment

  4. scapula orientation

    lateral scapular slide test

    Measured: Assessment procedure will be performed pre intervention and post third and sixth week of treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Aug 2024
  2. Study start30 Jul 2024
  3. Primary completion30 Jun 2025
  4. Study completion30 Jul 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
51 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06554860
Sponsor's protocol ID
Blackburn versus PNF
Acronym
impingment
Status last verified
Sep 2026
First submitted
18 Jul 2024
Last updated
5 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Aceituno-Gomez J, Avendano-Coy J, Gomez-Soriano J, Garcia-Madero VM, Avila-Martin G, Serrano-Munoz D, Gonzalez-Gonzalez J, Criado-Alvarez JJ. Efficacy of high-intensity laser therapy in subacromial impingement syndrome: a three-month follow-up controlled clinical trial. Clin Rehabil. 2019 May;33(5):894-903. doi: 10.1177/0269215518824691. Epub 2019 Jan 23.

    PubMed 30672303
  • AlHarbi Y. Anatomical Variations in the Pectoralis Minor Muscle Origin and Insertion: A Systematic Review. Cureus. 2023 Oct 1;15(10):e46329. doi: 10.7759/cureus.46329. eCollection 2023 Oct.

    PubMed 37916251
  • Abdul-Karim S, Abdul-Hamid MS, Ho CA, Ling J. Validity, Reliability and Responsiveness of the Malay Shoulder Pain and Disability Index (M-SPADI) for Patients with Shoulder Pain. Malays Orthop J. 2023 Mar;17(1):160-171. doi: 10.5704/MOJ.2303.019.

    PubMed 37064621
  • Alsanawi HA, Alghadir A, Anwer S, Roach KE, Alawaji A. Cross-cultural adaptation and psychometric properties of an Arabic version of the Shoulder Pain and Disability Index. Int J Rehabil Res. 2015 Sep;38(3):270-5. doi: 10.1097/MRR.0000000000000118.

    PubMed 25954858
  • An DI, Park JE, Lee CH, Kim SY. Reliability of scapular upward rotation and anterior-posterior tilt measurements using a modified digital inclinometer in patients with subacromial impingement syndrome. J Back Musculoskelet Rehabil. 2021;34(5):837-843. doi: 10.3233/BMR-200080.

    PubMed 33935062
  • Breckenridge JD, McAuley JH. Shoulder Pain and Disability Index (SPADI). J Physiother. 2011;57(3):197. doi: 10.1016/S1836-9553(11)70045-5.

    PubMed 21843839
  • Bot SD, Terwee CB, van der Windt DA, Bouter LM, Dekker J, de Vet HC. Clinimetric evaluation of shoulder disability questionnaires: a systematic review of the literature. Ann Rheum Dis. 2004 Apr;63(4):335-41. doi: 10.1136/ard.2003.007724.

    PubMed 15020324
  • Boykin RE, Friedman DJ, Zimmer ZR, Oaklander AL, Higgins LD, Warner JJ. Suprascapular neuropathy in a shoulder referral practice. J Shoulder Elbow Surg. 2011 Sep;20(6):983-8. doi: 10.1016/j.jse.2010.10.039. Epub 2011 Feb 1.

    PubMed 21277806
  • Blennow K, Brody DL, Kochanek PM, Levin H, McKee A, Ribbers GM, Yaffe K, Zetterberg H. Traumatic brain injuries. Nat Rev Dis Primers. 2016 Nov 17;2:16084. doi: 10.1038/nrdp.2016.84.

    PubMed 27853132
  • Boettcher CE, Ginn KA, Cathers I. The 'empty can' and 'full can' tests do not selectively activate supraspinatus. J Sci Med Sport. 2009 Jul;12(4):435-9. doi: 10.1016/j.jsams.2008.09.005. Epub 2008 Dec 2.

    PubMed 19054712
  • Cools AM, Vanderstukken F, Vereecken F, Duprez M, Heyman K, Goethals N, Johansson F. Eccentric and isometric shoulder rotator cuff strength testing using a hand-held dynamometer: reference values for overhead athletes. Knee Surg Sports Traumatol Arthrosc. 2016 Dec;24(12):3838-3847. doi: 10.1007/s00167-015-3755-9. Epub 2015 Aug 21.

    PubMed 26294055
  • Celik D, Dirican A, Baltaci G. Intrarater reliability of assessing strength of the shoulder and scapular muscles. J Sport Rehabil. 2012 Feb 29;21(1):1-5. doi: 10.1123/jsr.2012.TR3. Print 2012 Feb 1.

    PubMed 22495260
  • Cools AM, Cambier D, Witvrouw EE. Screening the athlete's shoulder for impingement symptoms: a clinical reasoning algorithm for early detection of shoulder pathology. Br J Sports Med. 2008 Aug;42(8):628-35. doi: 10.1136/bjsm.2008.048074. Epub 2008 Jun 3.

    PubMed 18523035
  • Consigliere P, Haddo O, Levy O, Sforza G. Subacromial impingement syndrome: management challenges. Orthop Res Rev. 2018 Oct 23;10:83-91. doi: 10.2147/ORR.S157864. eCollection 2018.

    PubMed 30774463
  • Curtis T, Roush JR. The Lateral Scapular Slide Test: A Reliability Study of Males with and without Shoulder Pathology. N Am J Sports Phys Ther. 2006 Aug;1(3):140-6.

    PubMed 21522226

Questions about this trial

What is this clinical trial studying?

A study testing scapular Blackburn stabilization plus exercise, PNF plus Exercise and exercise only in people with Impingement Syndrome, run by Cairo University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 11 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

shoulder pain and functional disability (time frame: Assessment procedure will be performed pre intervention and post third and sixth week of treatment). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06554860, which also lists 79 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Oct 2026.

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