Tulane iPredict, Prevent (TiPP) Study

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

To evaluate the progression of atrial myopathy through wearable devices and cardiac imaging.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 79
Healthy Volunteers: f
View:

⁃ Participants must meet the following criteria to be enrolled in the trial:

• Participants with atrial fibrillation aged 18 to 79 years old, or

• Participants aged 40 to 79 years old, at moderate or high risk for CVD as defined by the 10-year risk Atherosclerotic Cardiovascular Disease (ASCVD), a validated risk calculation tool.

• Participants who have access to internet/e-mail in their homes.

• Participants who have access to a compatible Android mobile device or compatible iOS mobile device (iPhone 4S or newer, iPad 3 or newer).

• Participants who are able and willing to return to the study clinic one-year following their baseline CMR for a follow-up appointment and 12-month CMR.

• Participants who are able to read, understand, and sign the consent form.

Locations
United States
Louisiana
Tulane University School of Medicine
RECRUITING
New Orleans
Contact Information
Primary
Quintrele Jones, MPH
qjones1@tulane.edu
504-988-3063
Backup
Chris Wang, MS
hwang37@tulane.edu
504-988-3065
Time Frame
Start Date: 2025-04-08
Estimated Completion Date: 2027-12
Participants
Target number of participants: 360
Treatments
Participants with Atrial Fibrillation or have Moderate-high risk factors for Atrial Fibrillation
Participants who have atrial fibrillation or have moderate to high-risk factors for the development of atrial fibrillation as verified by the Atherosclerotic CardioVascular Disease (ASCVD) risk calculation tool.~Participants will be provided with a Samsung Galaxy Watch to wear daily and will also be asked to wear an ECG patch for 30-days at baseline, 6, 9 and 12 months.~A Cardiac MRI (CMR) will be taken at baseline and at 12 months.
Related Therapeutic Areas
Sponsors
Leads: Tulane University School of Medicine
Collaborators: Samsung, Preventice

This content was sourced from clinicaltrials.gov

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