NCT04662541Completed
Mobile Integrated Health in Heart Failure
Using Mobile Integrated Health and Telehealth to Support Transitions of Care Among Heart Failure Patients - Parent Study
Source: ClinicalTrials.gov · Last updated 19 Feb 2026
Brief summary (registry, in English)
The purpose of this study is to compare how two different types of care after a hospitalization reduce hospital readmissions and symptom burden. The two types of care are a Transitions of Care Coordinator and Mobile Integrated Health. In the Transitions of Care Coordinator group, participants will receive a phone call from a care coordinator right after they go home following a hospitalization to check in. In the Mobile Integrated Health group, participants will be offered access to a community paramedic in case they need medical care while they are recovering at home after a hospitalization. The community paramedic will come to their home to perform an evaluation and set up a visit with an emergency physician via video conference. They may receive treatment at home or be transported to the emergency department. The investigators will be compare how well a Transitions of Care Coordinator and Mobile Integrated Health reduce readmissions to the hospital within 30 days of discharge and improve patient-reported health-related quality of life. The investigators hypothesize that participants in the Mobile Integrated Health group will have fewer readmissions to the hospital within 30 days of discharge and better health-related quality of life compared to participants in the Transitions of Care Coordinator group.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 2005 (actual)
- First submitted
- 4 Dec 2020
- Start date
- 4 Jan 2021
- Primary completion date
- 1 Nov 2024
- Lead sponsor
- Columbia University
- Diseases
- Heart failure
- NCT number
- NCT04662541
What you commit to
- Study type: Interventional
- Participants enrolled: 2005
- From 4 Jan 2021 to the primary completion date, 1 Nov 2024
- 3 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Anticipated discharge to, or currently receiving, hospice including home hospice
Other illness
- Diagnosis of dementia or psychosis
- Current candidate for and awaiting heart transplant
Other
- Non-English, Spanish, Mandarin, or French speaking
- Anticipated discharge to, or current residence in, skilled nursing facility or rehab center
- Current left ventricular assist device (LVAD)
Who the study is looking for
- Medicare or Medicaid recipient
- Current diagnosis of HF
- Receiving inpatient care at NewYork Presbyterian or Mount Sinai Health Systems
- Live in NYC
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Mount Sinai Health System Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Columbia University Irving Medical Center Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| New York - Presbyterian / Weill Cornell Medicine Coordinator of this site? Confirm its status | New York | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.