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.
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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
25
Post-discharge virtual visit
Weill Cornell Medicine
New York, New York, United States
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 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 who successfully complete video visit out of all of those who scheduled
Time frame: 6 months post-intervention
Patient satisfaction with the video visit
Based 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.
Time frame: Within one month post-intervention
Physician satisfaction with the video visit
Measured through multiple choice, yes/no, and free-response (only asked if specific responses are received) questions.
Time frame: Within one month post-intervention
Number of in-person visits instead of or in addition to video visit
Time frame: 6 months post-intervention
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