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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03291535
Other study ID # 12397
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 26, 2017
Est. completion date March 1, 2022

Study information

Verified date August 2022
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Investigators are examining the quality improvement impact of providing patients with a an electronic health record-connected blood pressure cuff. Investigators will give half of patients already eligible for hypertension management within a clinical pharmacist panel, the ability to upload their blood pressure data into Stanford's electronic health record.


Recruitment information / eligibility

Status Completed
Enrollment 75
Est. completion date March 1, 2022
Est. primary completion date March 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Hypertension as defined by clinical pharmacist usual care panel (2 or more readings of blood pressure >140/90) Exclusion Criteria: - Pregnancy - Chronic kidney disease III or IV - Systolic heart failure with ejection fraction <35% - Current use of 3 or more anti-hypertension drugs

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Connected-device
This intervention will allow patients to upload blood pressure data automatically from a blood pressure cuff into the electronic health record.
Usual care
This intervention will consist of usual clinical care as determined by the clinical pharmacist.

Locations

Country Name City State
United States Stanford Primary Care Portola Valley California
United States Stanford Primary Care Clinic Santa Clara California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in blood pressure over time in control group vs. the intervention group Difference in the change in blood pressure between the control group and intervention group. From enrollment to 6 months later
Secondary Patient visits Measurement of the number of in-person visits From enrollment to 6 months later
Secondary Patient remote interactions Measurement of the number of patient phone calls plus patient-portal messages to the clinical pharmacist From enrollment to 6 months later
Secondary Medication changes Number of changes in medication or medication dose From enrollment to 6 months later
Secondary Blood pressure control Time to reach target blood pressure control (Adults 18-59 years of age <140/90 mm Hg, Adults 60-85 years of age, without a diagnosis of diabetes, <150/90 mm Hg, Adults 60-85 years of age, with a diagnosis of diabetes, <140/90 mm Hg) From enrollment to 6 months later
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