Recruitment

Recruitment Status
Enrolling by invitation
Estimated Enrollment
Same as current

Summary

Conditions
  • Abnormal Heart Rhythms
  • Atrial Fibrillation
  • Cardiac Arrest
  • Cardiovascular Diseases
  • Cerebrovascular Accident
  • Coronary Heart Disease
  • Heart Attack
  • Heart Failure
  • Myocardial Infarction
  • Stroke
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Single (Participant)Masking Description: A set of existing Achievement members who have previously self-reported to meeting the inclusion criteria will be tagged for study inclusion, termed "participants". Since participants will be blinded to their study participation status, participants will not be asked to take any action to enroll in the study. In order to identify a target list of participants, Evidation Health will leverage already permissioned information from Achievement members, including data on their cardiovascular diagnoses, age, sex/gender, race/ethnicity, and country of residence.Primary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04584645
Collaborators
Sanofi Pasteur, a Sanofi Company
Investigators
Principal Investigator: Nell Marshall, DrPh Evidation Health