Blood Pressure Measuring Practice of Hong Kong Primary Care Doctors

November 21, 2019 updated by: Lee Kam Pui, Chinese University of Hong Kong

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

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

445

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Hong Kong, Hong Kong
        • Lek Yuen Clinic

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.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Doctors who regarded themselves working in Primary Care in Hong Kong

Description

Inclusion Criteria:

  • All doctors registered in the primary care directory in Hong Kong

Exclusion Criteria:

  • nil

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 Major Dates

Study Start (Actual)

May 3, 2019

Primary Completion (Actual)

September 30, 2019

Study Completion (Actual)

November 21, 2019

Study Registration Dates

First Submitted

April 19, 2019

First Submitted That Met QC Criteria

April 23, 2019

First Posted (Actual)

April 25, 2019

Study Record Updates

Last Update Posted (Actual)

November 25, 2019

Last Update Submitted That Met QC Criteria

November 21, 2019

Last Verified

November 1, 2019

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)?

UNDECIDED

IPD Plan Description

will share information when required by other researchers

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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