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Clinical Trials/NCT02551393
NCT02551393
Completed
Not Applicable

A Cluster-randomized Study on the Risk Assessment and Management Program for Home Blood Pressure Monitoring in Population With Inadequate Health Literacy

The University of Hong Kong0 sites291 target enrollmentApril 1, 2016
ConditionsHypertension

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
The University of Hong Kong
Enrollment
291
Primary Endpoint
Change in Clinic Blood Pressure control rate
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Clinical Trial: The investigators aims at comparing providing validated home BP device, followed by group education of self-management of hypertension as well as self-BP monitoring and appropriate medication in response to home BP reading, followed by nurse follow up with usual care, which may possibly improve patients with uncontrolled hypertensions drug adherence, and therefore improve their BP level in primary care setting. The investigators will invite total 270 patients from 5 general outpatient clinic (GOPCs) to participate the trial.

Qualitative study: The investigators would also like to evaluate patients' view and operational concerns on self BP monitoring by individually interviewing 30 selected patients with uncontrolled hypertension

Detailed Description

Background Recent oversea randomized control trials have proven effectiveness of lowering clinic and home BP if uncontrolled hypertensive patients were taught to perform home BP monitoring properly with validated BP device. Patients were taught to response to home BP reading (e.g. follow drug regime, or doctor adjust drug according to patients' home BP record) Study design 1. Prospective cluster randomized control trial, 2. Qualitative individual interview Aims The investigators aims at comparing providing validated home BP device, followed by group education of self-management of hypertension as well as self-BP monitoring and appropriate medication in response to home BP reading, followed by nurse follow up with usual care, which may possibly improve older adults with uncontrolled hypertension drug adherence, and therefore improve their BP level in a primary care setting. The investigators would also like to evaluate patients' view and operational concerns on self BP monitoring Subjects Adult Chinese on hypertensive treatment more than 12 months with uncontrolled hypertension by mean clinic BP measurement on the day of recruitment. Uncontrolled hypertension is defined as BP \> 140/90mmHg in subjects age \< 80; and BP \> 150/90mmHg in subjects age≥80. You will be invited to participate if you are willing and capable to perform self-home BP monitoring on daily basis. Sample size 270 (45 people from each clinic); 30 people for qualitative interview Assignment 3 clinics will be randomly assigned to intervention clinic while the other 2 will be randomly assigned to the control clinic (usual care) Intervention(s) Doctors and Nurses in intervention clinic will receive 1 hour briefing + education on the background, scientific basis and detail of the program during lunch time. Patients from intervention clinics will be invited to attend 2 x 2 hours education group (15-30 subjects / group) ran by clinic nurses and doctors. You will be educated on basic knowledge, management and drug for hypertension in the first session. In the 2nd session, a certified valid Home BP device will be loaned to you for 6- 9 months and you will be taught to perform home BP monitoring, record and respond to the BP reading accordingly. Upon completion of session 2, you will be arranged for nurse individual follow up after 4-8 weeks to see your progress and monitoring. 30 people with uncontrolled hypertension will be interviewed individually for their opinion on the program, management of hypertension and performance of home BP monitoring. Outcome measures BMI (BH/ BW), Waist circumference, Clinic BP (sitting position/ standing position), Lab Test: FBS, Lipid profile, eGFR, Urine PCR, ECG Qualitative data for patient's view on home BP monitoring Follow up duration 6-18months

Registry
clinicaltrials.gov
Start Date
April 1, 2016
End Date
December 30, 2018
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Sau-nga Fu

Ph D Student

The University of Hong Kong

Eligibility Criteria

Inclusion Criteria

  • on hypertensive treatment
  • uncontrolled hypertension by mean clinic BP measurement on the day of recruitment. Uncontrolled hypertension is defined as BP \> 140/90mmHg in subjects age \< 80; and BP \> 150/90mmHg in subjects age≥
  • willing and capable to perform home BP monitoring by themselves on daily basis. -

Exclusion Criteria

  • unable to perform the home monitoring either by themselves
  • mentally incapacitated
  • arrhythmias
  • unstable angina
  • serum creatinine \> 250 mmol/l
  • orthostatic hypotension
  • severe left ventricular impairment
  • severe aortic stenosis

Outcomes

Primary Outcomes

Change in Clinic Blood Pressure control rate

Time Frame: 18 months

After 18 months of treatment, to compare BP control rate in the intervention group and the control group.

Secondary Outcomes

  • Change of fasting blood sugar level(18 months)
  • Proportion of subjects with normal body mass index(18 months)
  • Change in mean clinic Systolic blood pressure (SBP) intervention group when compare with control group(6 months, 12 months and 18 months)
  • Qualitative study of patients' view and experience of home blood pressure monitoring(5 patients are interviewed before intervention, 6 weeks post-intervention, different time frame after patients' hypertension diagnosed)
  • Change of low density lipoprotein level (LDL)(18 months)
  • Change in mean clinic diastolic blood pressure DBP intervention group when compare with control group(6 months, 12 months and 18 months)

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