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Clinical Trials/NCT04236583
NCT04236583
Suspended
Not Applicable

Improving the Hospital-to-Home Transition Through Post-Discharge Virtual Visits in Primary Care

Weill Medical College of Cornell University1 site in 1 country25 target enrollmentFebruary 28, 2020
ConditionsTelehealth

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Telehealth
Sponsor
Weill Medical College of Cornell University
Enrollment
25
Locations
1
Primary Endpoint
Proportion of patients who consent to participate out of all those found to be eligible
Status
Suspended
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study is to test a new process for having a virtual visit with a primary care doctor after discharge from the hospital, instead of an in-person visit.

Detailed Description

The goal of this project is to fully develop the protocol for identifying patients who would benefit from a virtual visit and develop the protocol for implementing the virtual visit. The value of this project is that the results will provide ample preliminary data for a future randomized controlled trial to determine the effectiveness of the intervention. This project will have an intervention group only. The hypothesis is that the intervention can be implemented in a way that is feasible and acceptable to providers and patients.

Registry
clinicaltrials.gov
Start Date
February 28, 2020
End Date
December 2021
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Medical inpatients, age \>=18, with an existing WCIMA attending as his or her PCP
  • Patients with disposition to home
  • Medically appropriate for a video visit (as determined by inpatient attending)
  • Patients or caregivers must be able to enroll in MyChart before discharge, must be capable of using the Weill Cornell Connect app to do a video visit at home using broadband access or the equivalent (must own a device compatible with the app, e.g.
  • smartphone or tablet)
  • English speaking
  • Cognitively able to participate or Caregiver must be able to participate

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Proportion of patients who consent to participate out of all those found to be eligible

Time Frame: 6 months post-intervention

Proportion of patients who successfully schedule video visits out of all of those who consent

Time Frame: 6 months post-intervention

Proportion of patients meeting inclusion criteria over the study period out of all patients being discharged over the same time period

Time Frame: 6 months post-intervention

Proportion of patients who successfully complete video visit out of all of those who scheduled

Time Frame: 6 months post-intervention

Secondary Outcomes

  • Physician satisfaction with the video visit(Within one month post-intervention)
  • Patient satisfaction with the video visit(Within one month post-intervention)
  • Number of in-person visits instead of or in addition to video visit(6 months post-intervention)

Study Sites (1)

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