Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSF
Dates
study started
study ends around
Principal Investigator
by Alexis Beatty, MD, MAS (ucsf)
Headshot of Alexis Beatty
Alexis Beatty

Description

Summary

The goal of this study is to determine whether participation in a tailored cardiac rehabilitation program delivered in a safety net setting, compared to usual care referral to an outside cardiac rehabilitation program, results in greater participation in cardiac rehabilitation.

Keywords

Cardiac Rehabilitation, comparative effectiveness, safety net, Tailored cardiac rehabilitation, Referral to an external cardiac rehabilitation program, Tailored cardiac rehabilitation in a safety net setting

Eligibility

You can join if…

Open to people ages 18 years and up

  1. Age 18+
  2. Referred for cardiac rehabilitation for a covered indication:
    1. Acute myocardial infarction
    2. Percutaneous coronary intervention
    3. Coronary artery bypass surgery
    4. Heart valve repair or replacement
    5. Heart transplant
    6. Chronic stable angina
    7. Chronic systolic heart failure (EF <=35%)
  3. Able to communicate in English, Spanish, or Cantonese
  4. Able to consent for self

You CAN'T join if...

  1. Currently enrolled in hospice.
  2. Provider says patient may not be approached for participation in this study.

Location

  • Zuckerberg San Francisco General Hospital accepting new patients
    San Francisco 5391959 California 5332921 94110 United States

Lead Scientist at University of California Health

  • Alexis Beatty, MD, MAS (ucsf)
    Alexis Beatty, MD, MAS is a cardiologist and health services researcher who studies innovative delivery models for cardiovascular disease care to improve outcomes and reduce disparities. She received a career development award from the Department of Veterans Affairs to develop and test a mobile application to improve participation in cardiac rehabilitation, called VA FitHeart.

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT07158515
Study Type
Interventional
Participants
Expecting 100 study participants
Last Updated