MOON Shoulder Instability-Cohort of Patients Undergoing Operative Treatment.

Description

This project will be a multi-center, prospective longitudinal cohort for all patients undergoing primary shoulder instability surgery, excluding isolated SLAP repairs. We will be looking for risk factors for recurrent instability, revision surgery, and poor outcomes. Patients will be asked to complete the RAND-36, ASES, Shoulder Activity, EQ-5D and WOSI outcome measures, as well as demographic and socioeconomic information. Surgeons will complete a form after surgery with information on radiographic findings, physical exam, surgical findings, and the repair. Patients will wear a sling post-operatively, and follow standardized rehabilitation protocols, including physical therapy. Patients will be sent outcome questionnaires at 2, 6, 10, and 20 years after surgery.

Conditions

Other Instability, Shoulder, Dislocations, Subluxations, Recurrent Dislocation of Shoulder Region

Study Overview

Study Details

Study overview

This project will be a multi-center, prospective longitudinal cohort for all patients undergoing primary shoulder instability surgery, excluding isolated SLAP repairs. We will be looking for risk factors for recurrent instability, revision surgery, and poor outcomes. Patients will be asked to complete the RAND-36, ASES, Shoulder Activity, EQ-5D and WOSI outcome measures, as well as demographic and socioeconomic information. Surgeons will complete a form after surgery with information on radiographic findings, physical exam, surgical findings, and the repair. Patients will wear a sling post-operatively, and follow standardized rehabilitation protocols, including physical therapy. Patients will be sent outcome questionnaires at 2, 6, 10, and 20 years after surgery.

MOON Shoulder Instability-Cohort of Patients Undergoing Operative Treatment.

MOON Shoulder Instability-Cohort of Patients Undergoing Operative Treatment.

Condition
Other Instability, Shoulder
Intervention / Treatment

-

Contacts and Locations

San Francisco

UCSF Orthopedic Institute, San Francisco, California, United States, 94158

Boulder

University of Colorado, Boulder, Colorado, United States, 80304

Iowa City

University of Iowa, Iowa City, Iowa, United States, 52242

Lexington

University of Kentucky, Lexington, Kentucky, United States, 40536

Boston

Brigham and Women's Hospital, Boston, Massachusetts, United States, 02115

Ann Arbor

University of Michigan, Ann Arbor, Michigan, United States, 48109-0328

Saint Louis

Washington University, Saint Louis, Missouri, United States, 63110

New York

Hospital for Special Surgery, New York, New York, United States, 10021

Columbus

Ohio State University, Columbus, Ohio, United States, 43221

Sioux Falls

Orthopedic Institute, Sioux Falls, South Dakota, United States, 57105

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Workers compensation patients
  • * Prisoners
  • * Non-English speaker
  • * Not mentally competent
  • * Unable/unwilling to return for clinical follow-up
  • * Arthroplasty patients
  • * Rotator cuff tears
  • * Fractures

Ages Eligible for Study

12 Years to 99 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Carolyn M Hettrich,

Carolyn M Hettrich, MD, MPH, PRINCIPAL_INVESTIGATOR, Brigham and Women's Hospital

Brian Wolf, MD, MS, PRINCIPAL_INVESTIGATOR, University of Iowa

Study Record Dates

2042-12