Actively Recruiting
Tulane iPredict, Prevent Study to Evaluate the Progression of Atrial Myopathy.
Led by Tulane University School of Medicine · Updated on 2025-04-17
360
Participants Needed
1
Research Sites
138 weeks
Total Duration
On this page
Sponsors
T
Tulane University School of Medicine
Lead Sponsor
S
Samsung
Collaborating Sponsor
AI-Summary
What this Trial Is About
To evaluate the progression of atrial myopathy through wearable devices and cardiac imaging.
CONDITIONS
Official Title
Tulane iPredict, Prevent Study to Evaluate the Progression of Atrial Myopathy.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants aged 18 to 79 years with atrial fibrillation, or participants aged 40 to 79 years at moderate or high cardiovascular disease risk
- Access to internet and email at home
- Access to a compatible Android mobile device or an iPhone 4S or newer, or iPad 3 or newer
- Ability and willingness to return to the study clinic for a follow-up appointment and MRI scan one year after baseline
- Ability to read, understand, and sign the consent form
You will not qualify if you...
- Any health-related contraindications to gadolinium or MRI (e.g., allergy, pacemakers, implantable defibrillators, or other implants)
- Weighing more than 300 lbs (due to decreased MRI quality)
- Renal insufficiency with GFR less than 30 mL/min/1.73 m2 or acute/severe kidney disease
- Women who are pregnant at enrollment (no MRI if pregnant during study until 10 days postpartum)
- No access to internet or email
- No compatible Android or iOS mobile device
- Cognitive impairments affecting ability to use and maintain wearable devices
- Unable or unwilling to return for the one-year follow-up clinic visit and MRI
- Cognitive impairments preventing informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tulane University School of Medicine
New Orleans, Louisiana, United States, 70112
Actively Recruiting
Research Team
Q
Quintrele Jones, MPH
CONTACT
C
Chris Wang, MS
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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