Virtual Evaluation of Shoulder Range of Motion when Compared to Traditional In-Person Evaluation

Overview

About this study

The purpose of this study is to create and test the validity of a telehealth protocol for obtaining shoulder range of motion. 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Patients with glenohumeral osteoarthritis
  • Aged 60-80 years old
  • Patients can be pre or post surgical intervention via anatomic total shoulder arthroplasty or reverse total shoulder arthroplasty

Exclusion Criteria:

  • Patients with significant hearing impairment

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 11/20/2024. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Jonathan Barlow, M.D.

Contact us for the latest status

Contact information:

Ashley Keehn R.T.(R)(CT)

(507) 293-7131

Keehn.Ashley@mayo.edu

More information

Publications

Publications are currently not available