Verily Clinical Study Watch Analytical Validation Study

Verily Life Sciences

Status: Active, not recruiting

Conditions: Chronic Disease; Healthy Population

Treatments: Device: Verily Clinical Study Watch; Device: Vivalink ECG Patch; Device: Modus StepWatch 4

Study type: Observational

Funder types: Industry

Identifiers

NCT05534477

104126

Details and patient eligibility

About

This study is designed to evaluate the performance of the Verily Clinical Study Watch for the quantification of participants' movement and pulse rate when the wearer is at rest.

Enrollment: 100 estimated patients

Sex: All

Ages: 18 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Participant is ≥ 22 and ≤ 80 years old
• Participant understands the study requirements and is able and willing to provide written informed consent
• Participant is without significant limitation in ability to participate in the study, in the opinion of the investigator
• Participant owns a smartphone with a data plan and be the primary user of the smartphone; smartphone must be compatible with the applications used in the study
• Participant is a US Resident

Exclusion criteria

• Participant has tremor or significant life-threatening arrhythmia
• Participant is allergic to nickel or metal jewelry
• Participant has a known severe allergy to polyester, nylon, or spandex
• Participant has a known allergic reaction to adhesives or hydrogels
• Participant has a tattoo covering the area where the watch face would rest on either wrist
• Participant has planned international travel during the study