- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03926897
Blood Pressure Measuring Practice of Hong Kong Primary Care Doctors
Blood Pressure Measuring Practice of Hong Kong Primary Care Doctors: a Cross-sectional Study
Background: While office BP measurements were traditionally used to detect, diagnose and manage hypertension(HT), studies had convincingly showed that out-of-office blood pressure, including home blood pressure monitoring (HBPM) and ambulatory blood pressure monitoring (ABPM), was superior in predicting cardiovascular outcomes and death. Furthermore, some countries' guidelines suggested the use of validated automatic blood pressure machines (called automated office blood pressure monitoring (AOBP)) to screen for HT and record BP in routine HT clinical management. With difference between guidelines and various available BP measurement methods, it is not known how primary care doctors, who play the key role to detect and treat HT, are measuring BP in their daily practice.
Method: All doctors registered in the primary care directory will be mailed a questionnaire. Those who do not respond would be mailing for maximally 3 times, 2 weeks apart to enhance response rate. It is estimated that around 1500-2000 doctors will be eligible.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Hong Kong, Hong Kong
- Lek Yuen Clinic
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All doctors registered in the primary care directory in Hong Kong
Exclusion Criteria:
- nil
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
the blood pressure (BP) measurement method for screening of hypertension
Time Frame: 1 year
|
possible answers included: Manual BP in the office with mercury or aneroid device; Manual BP in the office with an electronic device; Automated office BP machines (AOBP) ; Other patient-activated electronic devices in the office; Electronic BP kiosks
|
1 year
|
|
The BP measurement method to diagnose hypertension
Time Frame: 1 year
|
possible answers included: Manual BP in the office with mercury or aneroid device; Manual BP in the office with an electronic device; Automated office BP machines (AOBP) ; Other patient-activated electronic devices in the office; Electronic BP kiosks; Ambulatory BP monitoring (24-hour to 48-hour BP monitoring); home BP monitoring
|
1 year
|
|
your routine methods used to measure BP in patients taking antihypertensive treatment (lifestyle or medications)
Time Frame: 1 year
|
possible answers included: Manual BP in the office with mercury or aneroid device; Manual BP in the office with an electronic device; Automated office BP machines (AOBP) ; Other patient-activated electronic devices in the office; Electronic BP kiosks; Ambulatory BP monitoring (24-hour to 48-hour BP monitoring); home BP monitoring
|
1 year
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SBRE-18-563
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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