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Clinical Trials/NCT02942940
NCT02942940
Unknown
Not Applicable

Conventional Follow-up Versus Mobile App Home Monitoring For Post-Operative Anterior Cruciate Ligament (ACL) Reconstruction Patients: A Randomized Controlled Trial

University of Toronto Orthopaedic Sports Medicine1 site in 1 country32 target enrollmentOctober 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anterior Cruciate Ligament (ACL) Tear
Sponsor
University of Toronto Orthopaedic Sports Medicine
Enrollment
32
Locations
1
Primary Endpoint
Required physician visits
Last Updated
9 years ago

Overview

Brief Summary

Background: Telemedicine is increasingly used to overcome distance between patients and physicians. Preliminary studies suggest that mobile app follow-up care for ACL reconstruction patients is feasible, can avert in-person follow-up care, and is cost-effective.

Objective: To avert in-person follow-up through the use of a mobile app in the first six weeks after surgery.

Methods: This will be a single-center, prospective randomized controlled trial

Results: Data to be analyzed from 72 patients.

Registry
clinicaltrials.gov
Start Date
October 2016
End Date
April 2018
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Toronto Orthopaedic Sports Medicine
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients undergoing ACL reconstruction at Women's College Hospital (WCH), between the ages of 18-
  • Patients must be able to use a mobile device and communicate in English.

Exclusion Criteria

  • Patients who are smokers, as they carry increased rates of complications.
  • Patients must not:
  • Suffer from chronic pain
  • Be taking narcotic (morphine-like) medication for pain on a regular basis, and
  • Have an allergy to local anesthetics or morphine-like medications
  • Pain scores captured in the VAS and QoR-9 are important for judging post-operative recovery. Pre-existing pain or inability to take narcotics post-operatively would compromise the reliability of these measures.

Outcomes

Primary Outcomes

Required physician visits

Time Frame: 6 weeks post surgery

Total number of physician visits (including specialist, family physician, and ER) related to surgery

Secondary Outcomes

  • Health care phone calls(6 weeks post surgery)

Study Sites (1)

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