Pectoralis Minor Release in Patients With Subacromial Impingement Syndrome

May 15, 2026 updated by: Walaa Mostafa Abd El-Haleem, Cairo University

Efficacy of Pectoralis Minor Release on Subacromial Space in Patients With Subacromial Impingement Syndrome

To investigate the effect of PMI release on subacromial space, pectoralis minor length, shoulders ROM, shoulder joint pain, and functional ability in patients with SAIS.

Study Overview

Detailed Description

Statement of the problem:

This study will be designed to answer the following question Does PMI release have an effect on subacromial space in patients with SAIS?

The purposes of the study:

  1. To investigate the effect of PMI release on subacromial space in patients with SAIS.
  2. To investigate the effect of PMI release on pectoralis minor length in patients with SAIS.
  3. To investigate the effect of PMI release on shoulders ROM (flexion, abduction, internal and external rotation) in patients with SAIS.
  4. To investigate the effect of PMI release on shoulder joint pain in patients with SAIS.
  5. To investigate the effect of PMI release on functional ability in patients with SAIS.

Study Type

Interventional

Enrollment (Estimated)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Dokki
      • Giza, Dokki, Egypt, 12612
        • Faculty of Physical Therapy Cairo University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Patients with chronic unilateral SAIS.
  2. Patient age average 40- 60 years old from both sexes (Michael and Gail 2000).
  3. Decreased AHD less than 10mm by x-ray image (Mean AHD in absence of rotator cuff tear is 10.5mm (Goutallier et al., 2011)).
  4. Decreased of active shoulder ROM.
  5. Presence of unilateral shoulder joint pain.
  6. Reliable patients.

Exclusion Criteria:

All patients who have any of the following will be excluded from the study (Lewis and Valentine 2007)

  1. Intra articular injection.
  2. Arthroscopic intervention.
  3. Previous shoulder fracture.
  4. Shoulder subluxation.
  5. Adhesive capsulitis.
  6. Shoulder osteoarthritis.
  7. Any previous operation on cervical and shoulder region.
  8. Mastectomy on the same side of shoulder impingement.
  9. Patients with neurological disorder that may contribute performance the procedure instructions.
  10. Osteoporosis.
  11. Pregnant and lactating woman.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Sham Comparator: traditional group
Thirty patients will receive traditional physical therapy treatment (Postural correction exercises and scapular stabilization exercises) at the painful shoulder, Treatment sessions will be two times per week for six weeks

Physiotherapy treatment included passive manual joint mobilization, home-based strengthening exercises and advice on posture, twice a week.

So, we will apply this conventional physical therapy to control group

  1. Postural correction exercise

    • Patient can apply this exercise on prone lie position for against a wall as in figure 10.
    • patient will start with chin in exercise, will asked to pull his chine in and push the wall, then hold for 15 seconds and repeat for 3 times.
    • Patient will try to touch both shoulders to the wall and hold for 15 seconds.
    • Patient will be asked to straight all spine against the wall and hold for 15 seconds.
  2. Scapular stabilization exercise Patient will lie prone with elbow extended, start to move his arm away from his body (horizontal abduction), with wait or without according to Lafayette muscle test results. Apply 2 cycle and each cycle will have 10 times repetitions
Experimental: Experimental Group
Thirty patients will receive traditional treatment plus pectoralis minor stretching and release, Treatment sessions will be two times per week for six weeks.

Physiotherapy treatment included passive manual joint mobilization, home-based strengthening exercises and advice on posture, twice a week.

So, we will apply this conventional physical therapy to control group

  1. Postural correction exercise

    • Patient can apply this exercise on prone lie position for against a wall as in figure 10.
    • patient will start with chin in exercise, will asked to pull his chine in and push the wall, then hold for 15 seconds and repeat for 3 times.
    • Patient will try to touch both shoulders to the wall and hold for 15 seconds.
    • Patient will be asked to straight all spine against the wall and hold for 15 seconds.
  2. Scapular stabilization exercise Patient will lie prone with elbow extended, start to move his arm away from his body (horizontal abduction), with wait or without according to Lafayette muscle test results. Apply 2 cycle and each cycle will have 10 times repetitions

Treatment will be conventional treatment with pectoralis minor release and stretch.

  • Pectoralis minor stretch The subject lying in a supine position with a towel roll running the length of the thoracic spine. The subject's shoulder at 90° of abduction and external rotation and the elbow at 90° flexion while therapist applying a posterior force to the coracoid process, in this study stretch will be performed for two sequential repetitions, holding the stretches for 30 seconds with 30 second break
  • Pectoralis minor release the subject in a supine position with the test arm at his side while the therapist palpated medially into the proximal axilla, followed by proceeding superiorly towards the coracoid process then applied pressure in the anterior direction, similar to attempting to lift the muscle, therapist applying tensile force directly to the pectoralis minor. The opposite therapist hand will stabilize the scapula and humeral head maintain for 30 seconds and repeat 2 times

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Subacromial space will be measured by X-ray image
Time Frame: 6 months
The radiograph will be done to measure acromio-humeral distance, which is considered the shortest distance between the inferior cortex of acromion and the top of humeral head. In normal shoulders, the sub acromial space was between 9 and 10 mm. The space was significantly greater in men, with a slight reduction with age. In middle age, a sub-acromial space less than 6 mm is pathological
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pectoralis minor length will be measured by tape measurement
Time Frame: 6 month

Participants will be asked to remain in a relaxed posture with the arms at the side in a neutral position, avoid postural correction, and exhale just before the measurement.

A tape measure was used to measure the linear distance between the origin and insertion of the muscle. The primary investigator of the study performed all measurements. The origin was defined as the inferior aspect of the 4th rib, which was one finger width lateral to the sternum, just lateral to the sternocostal junction. The insertion was defined as the medial-inferior aspect of the coracoid process .

6 month
Shoulder joint ROM (flexion, abduction, internal and external rotation) will be measured by inclinometer
Time Frame: 6 month

Shoulder flexion, abduction, internal and external rotation movements will be measured with the individual seated upright on a non-reclining high-back chair, to limit trunk compensation. The chair was the same for all movements performed by one individual, but different for each individual, to provide support up to the middle of the scapula.

Shoulder movements will be actively and passively evaluated for flexion in supine and seated positions, abduction, external rotation in a neutral position with 0° abduction (ERN), external rotation with the arm at 90° of abduction (ER90), and internal rotation with the arm at 90° of abduction (IR90) using an Acumar digital inclinometer .

6 month
Pain intensity will be measured by using VAS ( visual analog scale)
Time Frame: 6 month
The patients' pain severity will be evaluated using a visual analog scale (VAS). The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between 0 "no pain" and 10 "worst pain
6 month
Identification of Functional Ability of the shoulder joint using Q-DASH questionnaire with Arabic version
Time Frame: 6 month
The disabilities of the arm, shoulder and hand (DASH) questionnaire is a self-administered region-specific outcome instrument developed as a measure of self-rated upper extremity disability and symptoms The use of the DASH questionnaire as an outcomes instrument in patients with upper-extremity complaints. The main part of the Quick-DASH is a 14-item disability/symptom scale concerning the patient's health status during the preceding week. The items ask about the degree of difficulty in performing different physical activities as well as the problem's impact on social activities, work, sleep, and self-image. Each item has five response options. The scores for all items are then used to calculate a scale score ranging from 1 (no difficulty) to 5 ( unable).
6 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Abu EL Kasem Sh., Alaa F., Abd EL-Raoof N. et al., (2024):" Efficacy of Mulligan thoracic sustained natural apophyseal glides on sub-acromial pain in patients with sub-acromial impingement syndrome: a single-blinded randomized controlled trial "journal of manual & manipulative therapy 10.1080/10669817.2024.2341453 Amado A., Marques A., Maiorino R. et al., (2006):" An Anatomical Study of The Subcoracoid Space" CLINICS 2006;61(5):467-72 Ann Sisto S. and Dyson-Hudson T. (2007):" Dynamometry testing in spinal cord injury" Journal of Rehabilitation Research & Development, Volume 44, Number 1 Anne T., Herrington L., Horlsey I. et al. (2015):" An evidence-based review of current perceptions with regard to the subacromial space in shoulder impingement syndromes: Is it important and what influences it?" Clinical Biomechanics , Volume 30, Issue 7, August 2015, Pages 641-648

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 11, 2026

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

January 12, 2027

Study Registration Dates

First Submitted

May 10, 2026

First Submitted That Met QC Criteria

May 15, 2026

First Posted (Actual)

May 22, 2026

Study Record Updates

Last Update Posted (Actual)

May 22, 2026

Last Update Submitted That Met QC Criteria

May 15, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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