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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
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

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mount Sinai Health System
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Columbia University Irving Medical Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
New York - Presbyterian / Weill Cornell Medicine
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.