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

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

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04236583
Enrollment
25
Registered
2020-01-22
Start date
2020-02-28
Completion date
2021-12-31
Last updated
2020-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Telehealth

Keywords

Video Visits, Virtual Visits, Telehealth

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.

Interventions

OTHERTelehealth

Post-discharge virtual visit

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Proportion of patients meeting inclusion criteria over the study period out of all patients being discharged over the same time period6 months post-intervention
Proportion of patients who consent to participate out of all those found to be eligible6 months post-intervention
Proportion of patients who successfully schedule video visits out of all of those who consent6 months post-intervention
Proportion of patients who successfully complete video visit out of all of those who scheduled6 months post-intervention

Secondary

MeasureTime frameDescription
Physician satisfaction with the video visitWithin one month post-interventionMeasured through multiple choice, yes/no, and free-response (only asked if specific responses are received) questions.
Number of in-person visits instead of or in addition to video visit6 months post-intervention
Patient satisfaction with the video visitWithin one month post-interventionBased on a previously validated instrument (Parmanto et. al, Int J Telerehab 2016 Spring; 8(1): 3-10). Measured through 5-point likert scale,free response, multiple choice, and yes/no questions.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026