Motions of the Bones and Activation of the Muscles of the Shoulder Girdle During Basic and Common Arm Movement

Rotator Cuff Tears Clinical Trial

Official title:

Motions of the Bones and Activation of the Muscles of the Shoulder Girdle During Basic and Common Arm Movement

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04571268
• Other study ID #: 4030
• Status: Recruiting
• Start date: January 28, 2019
• Est. completion date: December 30, 2022

Study information

• Verified date: October 2021
• Source: More Foundation
• Contact: John D McCamley, PhD
• Phone: 634.241.8721
• Email: john.mccamley[@]more-foundation.org
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

A comprehensive understanding of healthy shoulder motion is a valuable contribution to the academic literature and provides a basis of comparison for various shoulder pathologies and treatments. However, the medical community is primarily interested in how pathology affects shoulder function and the underlying musculoskeletal reasons for impaired function associated with specific pathologies. Rotator cuff tears (RCT) provide an excellent model to study shoulder biomechanics because RCTs can cause significant functional impairment and can be quantified in size and location using standard clinical imaging techniques.

Upon completion of this study a comprehensive database of three-dimensional joint angles and EMG patterns of the structures of the shoulder joint complex of dominant and non-dominant during common activities of daily living will be available for healthy subjects and those of subjects whose dominant limbs are impaired by rotator cuff tears. These data will show normal muscle activations and movement patterns required to complete activities of daily living and compare them to the movement, and muscle activation patterns of persons who exhibit muscular and movement dysfunction due to rotator cuff tears.

Description:

Rotator cuff tears occur in approximately 20% of patients older than 65 years and increase with age. These non-traumatic RCTs are generally caused by normal age-related degeneration. Surgical treatment is effective, however recurrence of injury is common especially when the original tear was caused by age related degeneration. Non-surgical treatment options are designed to decrease pain and improve performance of activities of daily living and may be an effective alternative to surgery. If non-surgical treatment options are unsuccessful, surgical treatment may be considered. When rotator cuff tears are treated surgically, postoperative rehabilitation is an important factor in determining outcome success, however there is uncertainty regarding the best protocols for post-surgery rehabilitation. Evidence suggests that a more complete understanding of motion and muscle activation is necessary to design effective and reliable rehabilitation programs for rotator cuff injuries.

These data will enable medical professionals to better answer a range of clinical questions. They will provide health care professionals and researchers with a knowledge of relative muscle contributions to specific joint motions required to perform activities of daily living. This information is well suited to refine input variables for computer models and robotic testing platforms which can improve virtual and cadaver testing of shoulder impairment and repair models. Understanding the limitations to movement caused by RCT, and the resulting muscle activation patterns, will inform better surgical indications and enable therapists to better design rehabilitation protocols to enhance recovery from rotator cuff tears with or without surgery, as well as develop programs to limit future tears. Knowledge of muscle activation patterns during activities of daily living will also allow pre-habilitation protocols to be tailored for a subsequent surgical procedure such as reverse shoulder arthroplasty. These data will also assist in the design of shoulder prostheses whose biomechanical characteristics will compensate for deficiencies present in a shoulder joint impaired by rotator cuff injury. The knowledge gained from this study will provide a basis for future studies investigating traumatic shoulder injuries and the design of effective rehabilitation protocols for such injuries.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 45
• Est. completion date: December 30, 2022
• Est. primary completion date: December 30, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 50 Years to 70 Years

Eligibility

Inclusion Criteria:

All subjects

• Right hand dominant

• English speaking

• Subjects who have read and signed IRB approved informed consent for the study.

RCT subjects:

• Chronic right-side side shoulder pain with documented rotator cuff tear involving 2 or more tendons, and greater than 5cm as diagnosed by MRI

• Exhibit right rotator cuff disfunction without corresponding changes in the glenohumeral joint.

• Weakness of right rotator cuff isolated function based on clinical exam findings.

• Fatty infiltration grade 2 or more for involved muscle bellies based on MRI findings.

Exclusion Criteria:

• Unable to achieve 30º of external rotation and 140º of elevation in the scapular plane, where the limitations are not due to cuff tear associated pain.

• Diagnosis of osteoarthritis of the shoulder on their right side.

• History of musculoskeletal injury or disorder affecting any part of the right arm except the rotator cuff of the shoulder.

• History of musculoskeletal injury or disorder affecting any part of the left arm.

• Any musculoskeletal injury or disorder which prevents the subject standing unassisted for an extended period.

• Parkinson's disease.

• History of cerebral vascular accident.

• Pregnant.

• Current Incarceration.

Related Conditions & MeSH terms

• Rotator Cuff Injuries
• Rotator Cuff Tears

Locations

Country	Name	City	State
United States	MORE Foundation	Phoenix	Arizona

Sponsors (2)

Lead Sponsor	Collaborator
More Foundation	Depuy Synthes Products, Inc

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Range of motion	Measure range of motion in abduction, forward flexion, external rotation in neutral position and external rotation at 90 degrees abductions with corresponding rotator cuff muscle activation patterns	At enrollment
Primary	Activities of Daily Living	Measure glenohumeral joint angles and rotator cuff muscle activation patterns during the performance of prescribed activities of daily living	At enrollment
Secondary	Patient reported outcome	Completion of QuickDASH questionnaire	At enrollment