Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06070493
Other study ID # E-77082166-302.08.01-407339
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 19, 2022
Est. completion date June 1, 2023

Study information

Verified date September 2023
Source Gazi University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was planned to investigate the long-term effects of myofascial release technique on proprioception, pain severity, shoulder range of motion, functional level, flexibility, and muscle strength in patients with rotator cuff injury. The study included 29 individuals with partial rotator cuff injury who were randomly divided into two groups. The control group received a classical physiotherapy program including transcutaneous electrical nerve stimulation, hot pack and exercise, while the treatment group received the same classic physiotherapy program along with the myofascial release technique. All treatments were planned for 4 weeks and a total of 10 sessions. Proprioception, pain severity, shoulder range of motion, functional level, flexibility and muscle strength were assessed before and after the treatment.


Description:

Read more »
Read more »

Study Design


Related Conditions & MeSH terms


Intervention

Other:
classic physiotherapy program
For individuals of control group, a hot pack was applied to the shoulder area for 15 minutes, while the individuals were in the sitting position. The conventional mode of transcutaneous electrical nerve stimulation was used. Frequency was adjusted in the range of 50-100 Hz, and the amplitude intensity was adjusted between 10-30 milliampere with the intensity of mild tingling without causing any excessive discomfort or contractions. Electrodes were placed at the anterior, posterior, superior, and inferior of the shoulder region. In the exercise program of the patients, joint range of motion exercises, stretching, scapular stabilization, rotator cuff, and shoulder muscle strengthening exercises were given.
Myofascial release
myofascial release technique was applied to the patients in the treatment group besides the control group program. The technique was applied to the lateral neck and shoulder, pectoral region, scapulothoracic area, and arm regions for 5 minutes for optimum benefit.

Locations

Country Name City State
Turkey Gazi University Ankara Çankaya

Sponsors (1)

Lead Sponsor Collaborator
Gazi University

Country where clinical trial is conducted

Turkey, 

References & Publications (3)

Celik MS, Sonmezer E, Acar M. Effectiveness of proprioceptive neuromuscular facilitation and myofascial release techniques in patients with subacromial impingement syndrome. Somatosens Mot Res. 2022 Jun-Dec;39(2-4):97-105. doi: 10.1080/08990220.2021.2018293. Epub 2022 Jan 7. — View Citation

Gunes M, Yana M. Acute effects of thoracolumbar fascia release techniques on range of motion, proprioception, and muscular endurance in healthy young adults. J Bodyw Mov Ther. 2023 Jul;35:145-150. doi: 10.1016/j.jbmt.2023.04.063. Epub 2023 Apr 20. — View Citation

Nho SJ, Yadav H, Shindle MK, Macgillivray JD. Rotator cuff degeneration: etiology and pathogenesis. Am J Sports Med. 2008 May;36(5):987-93. doi: 10.1177/0363546508317344. Epub 2008 Apr 15. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Proprioception Proprioception is the joint position sense. Shoulder flexion, abduction and external rotation proprioception were measured with a digital inclinometer. Deviations between the targeted angle and the angle performed by the patients were noted. Baseline
Primary Proprioception Proprioception is the joint position sense. Shoulder flexion, abduction and external rotation proprioception were measured with a digital inclinometer. Deviations between the targeted angle and the angle performed by the patients were noted. After four weeks of treatment
Primary Pain severity Pain is an unpleasant sensation and emotional experience. The severity of pain at rest and during activity was evaluated using visual analog scale. The starting point of the line indicated "no pain" and the end point "unbearable pain" using a 10 cm horizontal line. Baseline
Primary Pain severity Pain is an unpleasant sensation and emotional experience. The severity of pain at rest and during activity was evaluated using visual analog scale. The starting point of the line indicated "no pain" and the end point "unbearable pain" using a 10 cm horizontal line. After four weeks of treatment
Secondary Range of motion Range of motion is the measurement of movement. Active shoulder flexion, abduction, and internal and external rotation range of motion measurements were performed bilaterally with a universal goniometer in the supine position. Baseline
Secondary Range of motion Range of motion is the measurement of movement. Active shoulder flexion, abduction, and internal and external rotation range of motion measurements were performed bilaterally with a universal goniometer in the supine position. After four weeks of treatment
Secondary Functional level Functional level was assessed by Shoulder Pain and Disability Index (SPADI). SPADI consists of a total of 13 items, 5 of which determine the level of pain and 8 items that determine the level of disability. Baseline
Secondary Functional level Functional level was assessed by Shoulder Pain and Disability Index (SPADI). SPADI consists of a total of 13 items, 5 of which determine the level of pain and 8 items that determine the level of disability. After four weeks of treatment
Secondary Flexibility The ability to move muscles and joints through a full normal range of motion. Flexibility of the internal and external rotator muscles of the shoulder was measured with the patient in the sitting position. The measurement was made by recording the distance between the middle fingers of both hands with a tape measure. Baseline
Secondary Flexibility The ability to move muscles and joints through a full normal range of motion. Flexibility of the internal and external rotator muscles of the shoulder was measured with the patient in the sitting position. The measurement was made by recording the distance between the middle fingers of both hands with a tape measure. After four weeks of treatment
Secondary Muscle strength Shoulder flexor, abductor, and internal and external rotator muscle strength were measured bilaterally using a digital hand dynamometer. Measurements were made with the patient in the sitting position. For all measurements, patients were asked to respond to the resistance for 3 seconds. All of the procedures were repeated 3 times and 1 minute rest was given between sets. Baseline
Secondary Muscle strength Shoulder flexor, abductor, and internal and external rotator muscle strength were measured bilaterally using a digital hand dynamometer. Measurements were made with the patient in the sitting position. For all measurements, patients were asked to respond to the resistance for 3 seconds. All of the procedures were repeated 3 times and 1 minute rest was given between sets. After four weeks of treatment
See also
  Status Clinical Trial Phase
Completed NCT04541953 - TeleRehabilitation Following Arthroscopic Rotator Cuff Repair N/A
Completed NCT04944446 - Myofascial Release in Shoulder Pathologies N/A
Recruiting NCT06112444 - Validity And Reliability Study Of The Turkish Version Of Short Western Ontario Rotator Cuff Index
Completed NCT04594408 - Tranexamic Acid to Improve Arthroscopic Visualization in Shoulder Surgery Phase 4
Active, not recruiting NCT04686396 - Demineralized Bone Matrix Rotator Cuff Study N/A
Recruiting NCT05988541 - Rotator Cuff Integrity and Clinical Outcomes 5 Years After Repair. N/A
Completed NCT04470167 - Phase 1/2 Clinical Study of TPX-115 in Patients With Partial-Thickness Rotator Cuff Tear Phase 1/Phase 2
Recruiting NCT05297305 - Onlay Versus Inlay Humeral Component in Reverse Total Shoulder Arthroplasty N/A
Completed NCT02528084 - The Effects of Yoga on Patients With Rotator Cuff Injuries N/A
Recruiting NCT05011331 - The Effect of a Custom Pillow on Sleep Quality in Patients With Nonoperative Rotator Cuff Syndrome N/A
Recruiting NCT04209504 - Evaluating Hemidiaphragmatic Paralysis With Prolonged Neural Blockade From an Interscalene Brachial Plexus Block
Completed NCT03967574 - Subacromial Corticosteroid Injections and tDCS in Rotator Cuff Tendinopathy N/A
Not yet recruiting NCT05906004 - Retrospective Data Collection and Prospective Clinical Investigation for the Augmentation or Reinforcement of the Rotator Cuff Using the Pitch-Patch
Completed NCT04952623 - Online Education to Improve the Management of Rotator Cuff Related Shoulder Pain N/A
Recruiting NCT05344898 - Subscap Reverse Shoulder Arthroplasty N/A
Recruiting NCT04175184 - Inclusion of Mobilisation With Movement to an Exercise Programme in Rotator Cuff Related Pain N/A
Terminated NCT05215600 - Anaverse™ Glenoid System and Its Instrumentation
Recruiting NCT05822414 - ESP vs STB for Pain and Diagraphragm Function for Shoulder Surgery N/A
Completed NCT04833244 - Automatic Multimodal Assessment of Occurrence and Intensity of Pain for Research and Clinical Use N/A
Completed NCT03982108 - Comparison of Two Arthroscopic Rotator Cuff Repair Techniques: Knot-tying Versus Knotless Suture-bridge Technique N/A