Actively Recruiting
FAPO-2: Cardiac Patient Monitoring Tool for Clinical Observation and Arrhythmia Detection
Led by University of Sao Paulo · Updated on 2025-09-15
520
Participants Needed
1
Research Sites
55 weeks
Total Duration
On this page
Sponsors
U
University of Sao Paulo
Lead Sponsor
S
Samsung Eletrônica da Amazônia Ltda
Collaborating Sponsor
AI-Summary
What this Trial Is About
The FAPO-2 study (Patient Monitoring Tool for Clinical Observation and Arrhythmia Detection) is a prospective, interventional, non-randomized study designed to evaluate the feasibility, usability, clinical effectiveness, and cost-efficiency of a wearable-enabled remote monitoring strategy in adult cardiac patients. The intervention consists of active clinical management of patients via teleconsultations, triggered by automated alerts generated through wearable data integrated into a centralized digital platform. FAPO-2 will include patients with chronic cardiovascular conditions and those undergoing recent minimally invasive interventions. The central objective is to validate a structured model for early arrhythmia detection, remote risk stratification, and timely clinical action. A total of 520 patients aged ≥22 years will be enrolled, stratified by sex (1:1), and followed at the Heart Institute (InCor) of the University of São Paulo. Participants will be allocated into one of four protocol groups: Group 1 - Pilot (n=15): Healthy volunteers monitored for \~14±3 days using both the smartwatch and a portable holter system to validate usability, skin tolerability, signal integrity, and data flow within the platform. Group 2 - Extensive Outpatient Monitoring (n=150): Patients with chronic cardiovascular diseases monitored over a 45-day period. During 30 days, monitoring will be performed using a smartwatch to capture blood pressure, oxygen saturation, heart rate, and single-lead ECG. For 15 days, participants will use both the smartwatch (for HR and ECG) and a portable holter system. Group 3 - Extensive Post-Intervention Monitoring (n=50): Patients recently undergoing procedures such as angioplasty, TAVI, or ablation, following the same monitoring protocol as Group 2. Group 4 - Optimized Outpatient Monitoring (n=305): Patients with stable chronic cardiac disease monitored for 15±3 days, using both devices simultaneously for HR and ECG (smartwatch) and portable holter system.
CONDITIONS
Official Title
FAPO-2: Cardiac Patient Monitoring Tool for Clinical Observation and Arrhythmia Detection
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients diagnosed with cardiovascular disease, of both sexes, aged over 22 years
- Signed informed consent form
- Willingness to follow study procedures and requirements
- Indicated for outpatient follow-up for cardiovascular condition or clinical need for surgical or catheter-based interventions
- Low or no risk of skin injury based on Braden Scale or clinical assessment
You will not qualify if you...
- Presence of skin conditions (vitiligo, lupus, atopic dermatitis) or wrist tattoos interfering with smartwatch readings
- Known allergy or sensitivity to wearable device components like adhesives or electrodes
- Inability to use wearable devices due to physical, cognitive, or technological limitations
- Presence of peripherally inserted central catheter (PICC) or arteriovenous fistula
- Implanted cardiac devices such as pacemakers, defibrillators, or cardiac resynchronization devices preventing ECG acquisition
- Diagnosed conditions causing blood pressure discrepancies between limbs (e.g., Stanford Type A aortic dissection, Takayasu arteritis, Subclavian Steal Syndrome, Kawasaki disease)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Instituto do Coracao, HCFMUSP
São Paulo, São Paulo, Brazil, 05403-900
Actively Recruiting
Research Team
F
Fabio B Jatene, PhD, MD
CONTACT
R
Rosangela Monteiro, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
4
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