Wrist-based Blood Pressure Monitoring Study
| Status: | Completed |
|---|---|
| Conditions: | High Blood Pressure (Hypertension) |
| Therapuetic Areas: | Cardiology / Vascular Diseases |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 1/10/2019 |
| Start Date: | May 7, 2018 |
| End Date: | December 31, 2018 |
A Pilot Study to Explore the Feasibility and Operational Pathways of Incorporating a Wrist-based Blood Pressure Monitoring Device Into the All of Us Research Program
To observe blood pressure variation in various real-world settings
This is an observational study, which will utilize a wrist-based blood pressure monitor to
explore blood pressure variation in up to 75 participants in various real-world settings.
There is no intervention in this study. The study will take place over a 4-week period.
During this time, participants will be asked to sample their blood pressures 1) at random
times, several times per day; 2) during specific periods of either emotional stress or
relaxation; 3) during guided orthostatic testing. Study participants will utilize an
application on their smartphones to log the device-measured blood pressures and flag selected
blood pressure measurements as either being part of the orthostatic testing or during periods
of emotional stress/relaxation. At the close of the study a post-study questionnaire will be
sent electronically to each participant.
explore blood pressure variation in up to 75 participants in various real-world settings.
There is no intervention in this study. The study will take place over a 4-week period.
During this time, participants will be asked to sample their blood pressures 1) at random
times, several times per day; 2) during specific periods of either emotional stress or
relaxation; 3) during guided orthostatic testing. Study participants will utilize an
application on their smartphones to log the device-measured blood pressures and flag selected
blood pressure measurements as either being part of the orthostatic testing or during periods
of emotional stress/relaxation. At the close of the study a post-study questionnaire will be
sent electronically to each participant.
Inclusion Criteria:
- Consortium members within the All of Us Research Program
- ≥18 years of age
- Own an iOS or Android device
Exclusion Criteria:
- Inability to give informed consent
- <18 years of age
- Inability to understand written English language
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