Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03494192
Other study ID # KA-180018
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2018
Est. completion date February 15, 2021

Study information

Verified date January 2022
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Abnormal reduction of the AHD has been considered as one of the possible mechanisms in the aetiology of subacromial pain syndrome. Maintenance of the AHD is crucial for prevention and rehabilitation of rotator cuff related disorders. The development of a rehabilitation treatment plan is based in part on the assessment of scapular motion and muscle deficits in patients with shoulder pain. Rehabilitation should be based on the identified impairments. The aim of this study is to investigate the effect of utilizing scapula retraction exercises with or without glenohumeral rotational exercises at gradual shoulder elevation angles into a scapular stabilization program on functionality, pain and AHD in patients with SPS and compare with health population.


Description:

Coordinated motion between the humerus and scapula is required for pain-free arm movement. Rotator cuff and scapulothoracic muscles dynamically control the subacromial space or acromiohumeral distance (AHD).Scapulothoracic muscles need to provide stability and control in a synchronized fashion to facilitate normal scapulohumeral movement. Scapular upward rotation and posterior tilt is essential to maintain the AHD.Therefore, the force couple function of the rotator cuff muscles play an critical role in opposing the superior migration force that is generated by deltoid muscle and, to maintenance the subacromial space. Abnormal reduction of the AHD has been considered as one of the possible mechanisms in the aetiology of subacromial impingement syndrome. Maintenance of the AHD is crucial for prevention and rehabilitation of rotator cuff related disorders. The development of a rehabilitation treatment plan is based in part on the assessment of scapular motion and muscle deficits in patients with shoulder pain. Rehabilitation should be based on the identified impairments. he aim of this study is to investigate the effect of utilizing scapula retraction exercises with or without glenohumeral rotational exercises at gradual shoulder elevation angles into a scapular stabilization program on functionality, pain and AHD in patients with SPS and compare with health population.


Recruitment information / eligibility

Status Completed
Enrollment 49
Est. completion date February 15, 2021
Est. primary completion date August 15, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - 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 - shoulder capsulitis.

Study Design


Intervention

Other:
Scapula Retraction Exercise Group
physiotherapy program consists of manual therapy, supervised stretching and scapulothoracic muscles strengthening exercises and home exercise programme including stretching and strengthening exercises will be applied two times a week total 24 sessions. After 24 sessions completed, patients will proceed to reduced exercise program until the 6-month follow-up.
Scapula Retraction +Glenohumeral Rotational Exercise Group
physiotherapy program consists of manual therapy, supervised stretching and scapulothoracic and also rotator cuff muscles strengthening exercises and home exercise programme including stretching and strengthening exercises will be applied two times a week total 24 sessions. After 24 sessions completed, patients will proceed to reduced exercise program until the 6-month follow-up

Locations

Country Name City State
Turkey Hacettepe University, Faculty of Health Sciences, Dept. of Physiotherapy and Rehabilitation Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other pain assessment pain intensity will de assessed by using Visual Analog Scale at rest, activity and at night. All assessment will be recorded at baseline, at the end of the 12-week treatment sessions and 6-month follow-up. from baseline to 6-month follow up
Other Acromiohumeral Distance Measurement Acromiohumeral Distance will be measured by 0°, 30°, 45°, 60° and 90° of shoulder abduction positions. All assessment will be recorded at baseline, at the end of the 12-week treatment sessions and 6-month follow-up. from baseline to 6-month follow up
Other Patient Satisfaction Patient Satisfaction will be assessed by simple questions consisting of self- recovery rate and patients expectation at 12 week and 6-month follow ups
Primary Functional Level Functional level will be assessed by using Shoulder Pain and Disability Index (SPADI). All assessment will be recorded at baseline, at the end of the 12-week treatment sessions and 6-month follow-up. ffrom baseline to twelve week after treatment sessions
See also
  Status Clinical Trial Phase
Terminated NCT03913702 - Subacromial Methylprednisolone Versus Ketorolac for Shoulder Impingement Phase 2
Completed NCT05071469 - Comparison of Two Different Treatment Methods N/A
Active, not recruiting NCT04660682 - A Comparison of the Long Term Effects of the Traditional and Modified Posterior Shoulder Stretching Exercise in Subacromial Impingement Syndrome N/A
Completed NCT03186287 - Effectiveness of Eccentric and Concentric Strength Training in Patients With Subacromial Impingement Syndrome N/A
Completed NCT04915430 - Training in Subacromial Impingement Syndrome N/A
Recruiting NCT01691157 - Exercise in the Physiotherapy Management of Shoulder Impingement N/A
Completed NCT01753271 - Subacute Effects of Spinal Mobilization to Treat Subacromial Impingement N/A
Withdrawn NCT01449448 - Subacromial Injection With Corticosteroid Versus Nonsteroidal Anti-inflammatory Drugs (NSAID) in Shoulder Impingement Syndrome N/A
Not yet recruiting NCT05794633 - Acupuncture Therapy in Patients With Subacromial Impingement Syndrome N/A
Active, not recruiting NCT06324487 - A New Application in Subacromial Impingement Syndrome N/A
Not yet recruiting NCT06023914 - Analysis of the Effect of Neuromuscular Electro-stimulation on the Performance of Isometric Rotator Cuff Strength. Phase 2/Phase 3
Recruiting NCT04644042 - The Effect of Arthroscopic Subacromial Decompression in Patients Who Are Non-responders to Non-operative Treatment. N/A
Completed NCT04594408 - Tranexamic Acid to Improve Arthroscopic Visualization in Shoulder Surgery Phase 4
Completed NCT05549674 - Copenhagen Cohort of Patients With Shoulder Pain
Completed NCT03888586 - Comparison of Dry Needling and Deep Friction Massage in Patients With Subacromial Pain Syndrome N/A
Completed NCT03303001 - Comparison Between Subacromial Infiltrations N/A
Recruiting NCT03658707 - Validity and Reliability of the Turkish Version of the Functional Shoulder Score
Recruiting NCT02374125 - Teres Major Muscle and Subacromial Impingement Syndrome N/A
Active, not recruiting NCT03326466 - Muscle Function, Central Nervous System Sensitization, and Pain Profiling in Patients With Subacromial Pain (SAP-CNSS).
Completed NCT04169880 - Effects of High Intensity Laser Therapy (HILT) in Patients With Subacromial Impingement Syndrome N/A