RECRUITING

Therapeutic Exercise for Rotator Cuff Tendinopathy / Subacromial Pain Syndrome - Outcomes and Mechanisms

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Conditions

Rotator Cuff TendinosisRotator Cuff TendinitisRotator Cuff InjuriesSubacromial Pain Syndrome

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Rotator cuff tendinopathy, one of the pathologies identified as part of the cluster of shoulder symptoms known as subacromial pain syndrome, is a common musculoskeletal shoulder condition. Resolution of pain and disability is poor despite treatment, with only about 50% reporting full recovery at 12 - 18 months. Prior studies suggest therapeutic exercise when used alone and with other interventions can have positive outcomes; however, not all patients with rotator cuff tendinopathy respond. Few studies have assessed the effects of exercise for individuals with chronic pain, especially brain driven mechanisms, thought to play a key role. In this study, we will use brain imaging to understand the mechanisms, identify predictors of a positive response to exercise, and the relationship to biomechanical and pain-related factors in patients with RC tendinopathy. The findings from this study will optimize the delivery and treatment response to exercise for individuals with shoulder pain.

Official Title

Mechanisms of Exercise for Rotator Cuff Tendinopathy / Subacromial Pain Syndrome

Quick Facts

Study Start:2021-06-08
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04923477

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.

Ages Eligible for Study:18 Years to 45 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. the clinical diagnosis for RC tendinopathy will be made with positive 3 of 5 tests: Hawkins-Kennedy, Neer, painful arc, empty can, external rotation resistance test
  2. 2. pain ≥ 3/10 on a numeric pain rating scale
  3. 3. age: 18 - 45 years
  4. 4. Participant must read, sign and date the appropriate Informed consent document.
  5. 5. Participant BMI ≤ 30
  1. 1. Insufficient ability to comprehend and complete the questionnaires,
  2. 2. Inability to attend sessions,
  3. 3. Prior surgery of shoulder, neck or thoracic spine,
  4. 4. Primary complaint of neck or thoracic pain,
  5. 5. Diagnosis of cervical spinal stenosis,
  6. 6. Any serious spinal and shoulder pathology: infections, arthrosis, rheumatic disorders, acute fractures, shoulder dislocation, osteoporosis, or tumors,
  7. 7. Central Nervous System involvement, to include hyperreflexia, sensory disturbances in the hand, intrinsic muscle wasting of the hands, unsteadiness during walking, nystagmus, loss of visual acuity, impaired sensation of the face, altered taste, the presence of pathological reflexes (i.e. positive Hoffman and/or Babinski reflexes,
  8. 8. two or more neurologic signs of nerve root compression to include myotomal weakness, positive muscle stretch reflex, and dermatomal sensory loss,
  9. 9. any shoulder or arm pain with cervical spine tests of Spurling's Test, cervical rotation to the ipsilateral side, or axial compression test, or
  10. 10. primary adhesive capsulitis defined by passive range of motion loss \>50% as compared bilaterally of shoulder external rotation, internal rotation, or elevation.
  11. 11. Has a device or other condition that is not safe for MRI, including pacemakers.

Contacts and Locations

Study Contact

Lori A Michener, PT, ATC, PhD
CONTACT
323-224-5032
lmichene@usc.edu

Principal Investigator

Lori A Michener, PT, ATC, PhD
PRINCIPAL_INVESTIGATOR
University of Southern California

Study Locations (Sites)

Clinical Biomechanics Orthopedic and Sports Outcomes Research Laboratory
Los Angeles, California, 90089
United States

Collaborators and Investigators

Sponsor: University of Southern California

  • Lori A Michener, PT, ATC, PhD, PRINCIPAL_INVESTIGATOR, University of Southern California

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 Registration Dates

Study Start Date2021-06-08
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2021-06-08
Study Completion Date2024-12-31

Terms related to this study

Additional Relevant MeSH Terms

  • Rotator Cuff Tendinosis
  • Rotator Cuff Tendinitis
  • Rotator Cuff Injuries
  • Subacromial Pain Syndrome