Trial Search Results

Feasibility Study to Improve AF Outcomes Using a Digital Application for CV Risk Reduction

The primary outcome of this prospective, RCT study is to determine the feasibility of utilizing AF CARE to provide lifestyle modification support to patients with AF.

The secondary outcome will compare the cardiovascular risk factors, AF knowledge, AF Symptom Severity and Burden, and QOL between and within the UC group and the CARE AF group at baseline, 3, and 6 months and 15 months.

Stanford is currently accepting patients for this trial.

Lead Sponsor:

Stanford University

Collaborator: American Heart Association

Stanford Investigator(s):


  • Device: AF CARE
  • Behavioral: Usual Care




Inclusion Criteria:

   1. BMI > 28 kg/m2 AND one additional CVRF using LS7

   2. Access and willingness to engage in digital technology

   3. Has a valid email address and a cell phone number

   4. Able to ambulate

   5. Able to speak/read English

Exclusion Criteria:

   1. Class III/IV heart failure

   2. MI or cardiac surgery in prior 3 months

   3. Severe renal/hepatic disease

   4. Active malignancy

   5. Current/recent (within 6 months) enrollment in weight loss program

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study


Now accepting new patients

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Linda K Ottoboni, PhD
Not Recruiting