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Scapula Retraction Exercises in Subacromial Pain Syndrome

Investigating the Effect of Scapula Retraction Exercises on Acromiohumeral Distance Values and Symptoms (Pain and Disability) in Patients With SPS

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04956757
Enrollment
42
Registered
2021-07-09
Start date
2021-07-30
Completion date
2023-06-17
Last updated
2024-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rotator Cuff Impingement Syndrome

Keywords

pain severity, functional status, acromiohumeral distance, shoulder pain

Brief summary

Scapula retraction exercises are often recommended as a part of the exercise programs. The primary aim of this study is to investigate the initial effect of the scapula retraction exercises on acromiohumeral distance (AHD) at varying shoulder abduction angles and to compare asymptomatic subjects. The secondary aim of this study is to investigate the effect of scapula retraction exercises on AHD values and symptoms (pain and disability) in patients with SPS.

Detailed description

Subacmial pain syndrome (SPS) is a common cause of shoulder pain and dysfunction in the general population. Exercise interventions is thought as a primary choice in clinical settings. Scapula retraction exercises are commonly recommended as a part of the exercise programs. Applying scapula retraction exercises at varying shoulder abduction angles could restore balance between the scapulothoracic muscles. Since the scapulothoracic muscles dynamically control subacromial space, scapula retraction exercises could further help to maintain AHD during arm elevation. The primary aim of this study is to investigate the initial effect of the scapula retraction exercises on acromiohumeral distance (AHD) at varying shoulder abduction angles and to compare asymptomatic subjects. The secondary aim of this study is to investigate the effect of scapula retraction exercises on AHD values and symptoms (pain and disability) in patients with SPS.

Interventions

OTHERExercise Intervention

Scapula retraction exercises at varying shoulder abduction angles will be applied

Sponsors

Hacettepe University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

Inclusion Criteria: * aged between 18-45 * painful arc of movement during flexion or abduction; * positive Neer or Kennedy-Hawkins impingement signs * pain on resisted lateral rotation, abduction or empty can test.

Exclusion criteria

* previous shoulder surgery; * shoulder pain reproduced by neck movement; * clinical signs of full-thickness RC tears; or * adhesive capsulitis.

Design outcomes

Primary

MeasureTime frameDescription
Acromiohumeral Distance (AHD) measurementAcromiohumeral distance values will be recorded at baseline and 8-week follow-upAcromiohumeral Distance will be recorded at 0°, 30°, 45°, 60° and 90° of shoulder abduction, and while they are doing scapular retraction with resistive elastic band at each shoulder position. All assessment will be recorded at baseline and at the end of the eight week rehabilitation sessions

Secondary

MeasureTime frameDescription
pain severitypain severity will be recorded at baseline and 8-week follow-uppain severity will be assessed by using 100 millimeters Visual Analogue Scale at rest, at night and during activity. All patients were asked to mark their pain level that corresponds to their pain intensity on the line between 0=no pain and 100=the worst pain imaginable.
disability statusPADI Score will be recorded at baseline and 8-week follow-updisability status will be assessed by using Shoulder Pain and Disability Index (SPADİ). All assessment will be recorded at baseline and at the end of the eight week treatment sessions. The questionnaire is scored on a 100-point scale, where 0 represents no disabilities and 100 represents extreme disabilities

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026