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Clinical Trials/NCT01079572
NCT01079572
Completed
Not Applicable

Cost-Effectiveness of Web-Based Follow Up Following Total Joint Arthroplasty

University of Western Ontario, Canada1 site in 1 country260 target enrollmentFebruary 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Osteoarthritis in the Knee Joint
Sponsor
University of Western Ontario, Canada
Enrollment
260
Locations
1
Primary Endpoint
Cost-effectiveness
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

Complications following total joint arthroplasty are rare, and the majority of follow-up visits are routine. The technology now exists to conduct annual follow-up assessments without having to physically see the patient.

This study will investigate the cost-effectiveness of web-based follow-up assessments compared to standard in-clinic follow-ups. We will also assess patient satisfaction, preference, and the validity of the web-based follow up assessments. Patients coming up to their 1 year follow-up or greater will be randomized to either the web-based group or the usual care group.

Web-based patients will complete all questionnaires using an online database system, and have their x-ray taken at their local radiology facility. The surgeon will review radiographs online. If there are any concerns with the x-ray or responses to questionnaires, arrangements will be made for the patient to be seen at the clinic. Patients in the Usual Care group will come into the clinic for their follow-up assessment and have their x-ray taken at University Hospital as usual.

Online assessment could significantly decrease wait times in orthopaedic clinics, as well as increase availability for OR time and new consultations. This approach could also potentially reduce patient burden by decreasing travel distances, financial burden and time requirements.

Registry
clinicaltrials.gov
Start Date
February 2010
End Date
March 2011
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Western Ontario, Canada
Responsible Party
Principal Investigator
Principal Investigator

Dianne Bryant

Associate Professor

University of Western Ontario, Canada

Eligibility Criteria

Inclusion Criteria

  • patients who have had a primary total hip or total knee arthroplasty

Exclusion Criteria

  • patients with osteolysis, or previous complications from their joint replacement

Outcomes

Primary Outcomes

Cost-effectiveness

Time Frame: one year

Secondary Outcomes

  • Harris Hip Score(one year)
  • Western Ontario and McMaster Osteoarthritis Index (WOMAC)(one year)
  • SF-12(one year)
  • Adverse events(one year)

Study Sites (1)

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