RECRUITING

Comparison of Cuff-Less Wrist Wearable Blood Pressure Device to Cuff Based Blood Pressure Measuring Devices

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

(1) To compare cuff-less wrist wearable radial artery blood pressure measurements utilizing ViTrack(developed by Dynocardia) to the cuff based commercially available blood pressure device, in healthy volunteers with normal or high blood pressure.

Official Title

Comparison of Cuff-Less Wrist Wearable to Cuff Based Commercial Available Blood Pressure Measuring Devices in Health Volunteers With Normal or High Blood Pressure

Quick Facts

Study Start:2021-01-01
Study Completion:2025-12-21
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04835857

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 90 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Health volunteers 18 years and above; equal numbers of males and females to address Sex As a Biological Variable (SABV); and in sinus rhythm.
  2. * Agree to commit to participate in the current protocol.
  3. * Provide written informed consent prior to any study procedures being performed (all subjects should be able to understand the informed consent form and any other documents that subjects are required to read).
  1. * Unable or unwilling to provide informed consent
  2. * Any other condition that would increase the risk of participation in the study in the opinion of the site Investigator.
  3. * A difference of \>10 mm Hg in left versus right arm oscillometric systolic BP.
  4. * Upper extremity arteriovenous hemodialysis shunt.
  5. * Wrist distortion or pain from arthritis.
  6. * Prior trauma or surgery at the radial artery monitoring site.

Contacts and Locations

Study Contact

Mohan Thanikachalam, MD
CONTACT
+1 (617) 639 - 5569
admin@dynocardia.care
Gokul Prasath Rajamanickam, MS
CONTACT
gokulpr@dynocardia.care

Principal Investigator

Mohan Thanikachalam, MD
PRINCIPAL_INVESTIGATOR
Dynocardia, Inc

Study Locations (Sites)

Dynocardia Inc
Newton, Massachusetts, 02459
United States

Collaborators and Investigators

Sponsor: Dynocardia, Inc

  • Mohan Thanikachalam, MD, PRINCIPAL_INVESTIGATOR, Dynocardia, Inc

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-01-01
Study Completion Date2025-12-21

Study Record Updates

Study Start Date2021-01-01
Study Completion Date2025-12-21

Terms related to this study

Keywords Provided by Researchers

  • Blood Pressure, Cuff less, Wearable, BP

Additional Relevant MeSH Terms

  • Hypertension
  • Healthy