About this trial

This study will collect physiologic data in patients with cardiovascular conditions and observe the natural history of those conditions for research purposes.

Eligibility criteria

Qualifiers

18 years of age and older

Ability to understand study assessments and give informed consent to data collection

Ability to comply with the study protocol

Ability to understand and respond to instructions in English

Disqualifiers

Allergy to adhesive used in biosensor patch

Life threatening disease process outside of area under study, such as actively treated cancer or pre/post-transplant such as hepatic failure; end-stage renal disease.

Severe CVD defined by hospital admission for cardiac diagnosis within 30 days of enrollment or documentation of NYHA functional class IV

Self-reported weight of 400 pounds or greater

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

5,000 Participants
are grouped into 1 trial group

Locations

1
Prolaio60606, ChicagoIllinois, United States

Sponsors and collaborators

Prolaio

Lead sponsor