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Feasibility Study to Improve AF Outcomes Using a Digital Application for CV Risk Reduction
Not Recruiting
Trial ID: NCT04050982
Purpose
The pilot portion of this study is to determine the feasibility of utilizing AF CARE to
provide lifestyle modification support to patients with atrial fibrillation (AF).
The prospective, RCT portion of this study compare cardiovascular risk factors (CVRF), AF
knowledge, AF Symptom Severity and Burden, and QOL between and within the wait list group and
the AF CARE group at baseline, 3, 6, and 12 months.
Official Title
Feasibility Study to Improve Atrial Fibrillation Outcomes Using a Digital Application for Cardiovascular Risk Reduction: Precursor to a Multicenter Randomized Trial
Stanford Investigator(s)
Linda K. Ottoboni, PhD, CNS
Clinical Assistant Professor, Medicine - Primary Care and Population Health
Eligibility
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
Intervention(s):
device: AF CARE
behavioral: Usual Care
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Linda K Ottoboni, PhD
650-498-5914