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Clinical Trials/NCT01991782
NCT01991782
Completed
Not Applicable

The Impact of Telemedicine on Orthopaedic Trauma Patients With Closed Fractures

Vanderbilt University1 site in 1 country20 target enrollmentJune 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Telemedicine
Sponsor
Vanderbilt University
Enrollment
20
Locations
1
Primary Endpoint
Patient Satisfaction and Clinical Outcomes at Conclusion
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to determine whether telemedicine video calls for follow-up visits between patients and their orthopaedic trauma surgeons has an impact on patient satisfaction, quality of life, and treatment adherence. This study will also assess the feasibility of telemedicine as a medium for follow-up visits.

Detailed Description

Patients who are over the age of 18 years with closed fractures treated at Vanderbilt University Medical Center by the Orthopaedic Trauma Department will be recruited into the study into one of two arms: a telemedicine arm in which the patient will have some of his or her visits conducted through video calls, and a control arm in which all of the visits for the patient will be in-person at the Vanderbilt University Orthopaedic Trauma Clinic. Comparisons between the two groups will be made through surveys administered to the patients half-way through the study and at the conclusion of the study, and comparisons will be made using standard statistical tests. The feasibility of telemedicine as a medium for follow-up visits in lieu of in-person visits will be assessed in this study.

Registry
clinicaltrials.gov
Start Date
June 2012
End Date
June 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Manish Sethi

Assistant Professor of Orthopaedics

Vanderbilt University

Eligibility Criteria

Inclusion Criteria

  • adults over 18 years old with closed fracture and having access to telemedicine technology (i.e. high speed Internet) at home

Exclusion Criteria

  • patients as part of vulnerable populations

Outcomes

Primary Outcomes

Patient Satisfaction and Clinical Outcomes at Conclusion

Time Frame: 6 month

Surveys will be administered to all patients in both arms of the study at the conclusion of the study to assess patient satisfaction with their treatment arms. Furthermore, all clinical outcomes for patients with be addressed at this point to note fracture healing status, any development of complications, and any redefinition of goals of care.

Study Sites (1)

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