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Per IRB COVID-19 guidance on conducting human subjects research
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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Telehealth | Experimental | 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. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Telehealth | Other | Post-discharge virtual visit |
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| Measure | Description | Time Frame |
|---|---|---|
| Proportion of patients meeting inclusion criteria over the study period out of all patients being discharged over the same time period | 6 months post-intervention | |
| Proportion of patients who consent to participate out of all those found to be eligible | 6 months post-intervention | |
| Proportion of patients who successfully schedule video visits out of all of those who consent | 6 months post-intervention | |
| Proportion of patients who successfully complete video visit out of all of those who scheduled | 6 months post-intervention |
| Measure | Description | Time Frame |
|---|---|---|
| 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. | Within one month post-intervention |
| Physician satisfaction with the video visit |
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Inclusion Criteria:
smartphone or tablet)
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| Name | Affiliation | Role |
|---|---|---|
| Sanjai Sinha, MD | Weill Medical College of Cornell University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Weill Cornell Medicine | New York | New York | 10065 | United States |
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| ID | Term |
|---|---|
| D017216 | Telemedicine |
| ID | Term |
|---|---|
| D003695 | Delivery of Health Care |
| D010346 | Patient Care Management |
| D006298 | Health Services Administration |
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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 | 6 months post-intervention |