Following Heart Conditions Over Time Using Digital Monitoring Devices
Observes how long-term heart and blood pressure conditions change, using digital monitoring devices.
Plain-language title generated from the registry record
Registry title: Study of the Progression of Chronic Cardiovascular Conditions
Key facts
- Where
- Chicago, United StatesSee the site
Where in United States
- ProlaioChicago, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Prolaio
- Trial code
- NCT07420907
- Record updated
- 12 August 2026
- Original description
This study will collect physiologic data in patients with cardiovascular conditions and observe the natural history of those conditions for research purposes.Read full original descriptionShow less
A Non-interventional Observational Study of the Sustained Use of Prolaio Digital Health Devices to Monitor the Natural History of Chronic Cardiovascular Conditions in Ambulatory Patients
This study will collect physiologic data in patients with cardiovascular conditions and observe the natural history of those conditions for research purposes.
Inclusion: 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; Has diagnosis of qualifying Cardiovascular Disease(s), including but not limited to: HF, AS, HCM, HTN, DCM, etc. Additional CVD may be included at discretion of the investigators; Resides in the United States.
Exclusion: Allergy to adhesive used in biosensor patch; Life-threatening disease process outside of area under study, such as actively treated cancer or being actively considered for organ pre-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; -- For participants who do not qualify due to this exclusion, and have not been hospitalized within 30 days of enrollment, they may reapply to enroll in the study; Self-reported weight of 400 pounds or greater.