- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04236583
Improving the Hospital-to-Home Transition Through Post-Discharge Virtual Visits in Primary Care
April 6, 2020 updated by: Weill Medical College of Cornell University
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.
Study Overview
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.
Study Type
Interventional
Enrollment (Anticipated)
25
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
New York, New York, United States, 10065
- Weill Cornell Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Telehealth
Eligible patients will be given the option to consent to having one virtual visit with their primary care physician within four weeks after discharge from the hospital.
Usual follow-up care will occur during this visit.
|
Post-discharge virtual visit
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
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
|
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
|
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
|
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
|
6 months post-intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient satisfaction with the video visit
Time Frame: Within one month post-intervention
|
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.
|
Within one month post-intervention
|
Physician satisfaction with the video visit
Time Frame: Within one month post-intervention
|
Measured through multiple choice, yes/no, and free-response (only asked if specific responses are received) questions.
|
Within one month post-intervention
|
Number of in-person visits instead of or in addition to video visit
Time Frame: 6 months post-intervention
|
6 months post-intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Sanjai Sinha, MD, Weill Medical College of Cornell University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
February 28, 2020
Primary Completion (ANTICIPATED)
December 1, 2021
Study Completion (ANTICIPATED)
December 1, 2021
Study Registration Dates
First Submitted
January 17, 2020
First Submitted That Met QC Criteria
January 17, 2020
First Posted (ACTUAL)
January 22, 2020
Study Record Updates
Last Update Posted (ACTUAL)
April 8, 2020
Last Update Submitted That Met QC Criteria
April 6, 2020
Last Verified
April 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 19-09020793
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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