search
Back to results

Management of Hypertension and Multiple Risk Factors to Enhance Cardiovascular Health

Primary Purpose

Hypertension, Cardiovascular Disease

Status
Unknown status
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
Structured Multicomponent Intervention (MCI)
Sponsored by
Duke-NUS Graduate Medical School
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Hypertension focused on measuring Blood Pressure, Lipids, Cardiovascular, Health Services, Hypertension

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 40 years or older
  • Singapore citizens or Permanent Residents
  • Visiting the recruiting polyclinic at least twice during the last 1 year
  • Individuals with a diagnosis of hypertension (systolic BP ≥ 140 mm Hg or diastolic BP ≥ 90 mm Hg on two or more prior visits; physician diagnosed hypertension, or on antihypertensive medications) and uncontrolled blood pressure (systolic BP ≥ 140 mm Hg or diastolic BP ≥ 90 mm Hg)

Exclusion Criteria:

  • Active systemic illness including fever, recent hospitalization (i.e. during last 4 months),
  • Clinically unstable heart failure or advanced kidney disease {estimated CKD-Epi glomerular filtration rate (GFR) <40 ml/min/1.73m2 or nephrotic range proteinuria (i.e. 3g/d or more)},
  • Known liver disease,
  • Pregnancy or breastfeeding
  • Any other major debilitating disease or mental illness that precludes validity of informed consent

Sites / Locations

  • SingHealth Polyclinics (SHP)Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Usual Care

Arm Description

Structured multicomponent intervention (MCI)

Control group receive usual care in the polyclinics

Outcomes

Primary Outcome Measures

Change in Systolic Blood Pressure from baseline to final follow-up at 24 months

Secondary Outcome Measures

Change in serum LDL from baseline to final follow-up at 24 months
Proportion of hypertensive individuals with BP controlled to target or > 5 mm Hg decrease in systolic BP
Proportion of hypertensive individuals with decrease in LDL cholesterol by >0.4 mmol/L (>15 mg/dl).
Composite outcome of death or hospital admission due to Coronary heart disease (CHD), heart failure, or stroke
Individual outcomes of all-cause mortality, Cardiovascular disease (CVD) deaths, and hospital admission due to CHD, heart failure, or stroke
Decrease of > 0.5 percent in glycated hemoglobin or change in proportion of hypertensive individuals with glycated hemoglobin <7% in hypertensive individuals with diabetes
Change in albuminuria from baseline to follow-up at 24 months
Change in estimated CKD-EPI GFR from baseline to follow-up at 24 months
Change in cardiovascular disease (CVD) risk score
Individual outcomes of change in a) diastolic BP and b) total cholesterol from baseline to end of follow-up at 24 months
Change in lifestyle (diet, physical activity based on self-report) or BMI between groups
Change in systolic blood pressure from baseline to 12 months
Change in serum LDL cholesterol from baseline to 12 months

Full Information

First Posted
November 20, 2016
Last Updated
January 30, 2018
Sponsor
Duke-NUS Graduate Medical School
Collaborators
SingHealth Polyclinics
search

1. Study Identification

Unique Protocol Identification Number
NCT02972619
Brief Title
Management of Hypertension and Multiple Risk Factors to Enhance Cardiovascular Health
Official Title
Management of Hypertension and Multiple Risk Factors to Enhance Cardiovascular Health - A Cluster Randomized Trial in Singapore Polyclinics
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Unknown status
Study Start Date
January 15, 2017 (Actual)
Primary Completion Date
March 15, 2020 (Anticipated)
Study Completion Date
March 15, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Duke-NUS Graduate Medical School
Collaborators
SingHealth Polyclinics

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Hypertension is a serious public health problem responsible for significant mortality and morbidity from cardiovascular disease. In Singapore, 1 in 4 adults age 30 years or older suffer from hypertension. Nearly half of these patients have uncontrolled hypertension and only 50% of individuals are on antihypertensive treatment. Our study aims to evaluate the effectiveness, cost effectiveness and impact on medication adherence of a well-structured program using multicomponent intervention for hypertension control aimed at overall cardiovascular risk reduction among individuals with hypertension attending the polyclinics in Singapore, compared to existing services. Such a program is expected to be cost-effective in terms of improving hypertensive individuals' outcomes, and to be potentially scalable and sustainable. Methods/design: Cluster randomized trial of 8 of the nine SingHealth Polyclinics randomized to intervention or usual care (4 each) and followed up for 2 years post randomization Intervention: The structured multicomponent primary care program comprises of: 1) algorithm-driven antihypertensive treatment for all hypertensive individuals and using fixed-dose combination (FDC) and lipid-lowering medication for high-risk hypertensive individuals, 2) motivational conversation for high-risk hypertensive individuals, 3) Follow-up of all hypertensive individuals on improving blood pressure (BP) as a primary outcome and other cardiovascular risk factors as a secondary outcome, and 4) discounts on FDC antihypertensive medication Usual care: The participants attending polyclinics randomized to usual care will continue to receive treatment from the health providers according to existing practices. The hypertensive individuals will also continue to pay for the services (physician or nurse consultation) as per their existing model of reimbursement. Participants: A total of 1000 participants will be recruited, 125 from each of the 8 polyclinics. Recruitment will be in batches of 4 and 4 clinics sequentially (balanced by randomization group). Outcomes: All hypertensive individuals will be assessed by trained outcomes assessors independent to treatment at baseline, 1-year and 2-yeat post randomization. The primary outcome will be the change in systolic blood pressure from baseline to 2 years. Primary Cost-Effectiveness measures will be- 1) Incremental cost per mm Hg systolic BP reduction from baseline to end of follow-up at two years post randomization; 2) incremental cost per projected CVD disability adjusted life years (DALYs) averted and quality adjusted life years (QALYs) saved, and 3) incremental cost per change in cardiovascular risk score from baseline to final follow-up at two-year post. The impact of effect on adherence to antihypertensive and lipid medication will be measured using data on adherence obtained from polyclinic pharmacy records and clinic notes. An average of percent adherence to antihypertensive and lipid lowering will be computed as a composite score. The change in percent composite adherence to antihypertensive and lipid medications from baseline to follow up will be compared between the intervention and control groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Cardiovascular Disease
Keywords
Blood Pressure, Lipids, Cardiovascular, Health Services, Hypertension

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Structured multicomponent intervention (MCI)
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Control group receive usual care in the polyclinics
Intervention Type
Other
Intervention Name(s)
Structured Multicomponent Intervention (MCI)
Intervention Description
Multicomponent Intervention (MCI) includes 1) algorithm-driven antihypertensive treatment for all hypertensive individuals using fixed-dose combination (FDC) and lipid lowering for high risk hypertensive individuals, 2) motivational conversation for high-risk hypertensive individuals and 3) telephone based follow-ups of all hypertensive individuals by a team of physician supervised nurse, and 4) discounts on FDC antihypertensive medications
Primary Outcome Measure Information:
Title
Change in Systolic Blood Pressure from baseline to final follow-up at 24 months
Time Frame
Baseline to 2 years
Secondary Outcome Measure Information:
Title
Change in serum LDL from baseline to final follow-up at 24 months
Time Frame
Baseline to 2 years
Title
Proportion of hypertensive individuals with BP controlled to target or > 5 mm Hg decrease in systolic BP
Time Frame
Baseline to 2 years
Title
Proportion of hypertensive individuals with decrease in LDL cholesterol by >0.4 mmol/L (>15 mg/dl).
Time Frame
Baseline to 2 years
Title
Composite outcome of death or hospital admission due to Coronary heart disease (CHD), heart failure, or stroke
Time Frame
2years
Title
Individual outcomes of all-cause mortality, Cardiovascular disease (CVD) deaths, and hospital admission due to CHD, heart failure, or stroke
Time Frame
2 years
Title
Decrease of > 0.5 percent in glycated hemoglobin or change in proportion of hypertensive individuals with glycated hemoglobin <7% in hypertensive individuals with diabetes
Time Frame
Baseline to 2 years
Title
Change in albuminuria from baseline to follow-up at 24 months
Time Frame
Baseline to 2 years
Title
Change in estimated CKD-EPI GFR from baseline to follow-up at 24 months
Time Frame
Baseline - 2 years
Title
Change in cardiovascular disease (CVD) risk score
Time Frame
Baseline - 2 years
Title
Individual outcomes of change in a) diastolic BP and b) total cholesterol from baseline to end of follow-up at 24 months
Time Frame
Baseline to follow-up 2 years
Title
Change in lifestyle (diet, physical activity based on self-report) or BMI between groups
Time Frame
Baseline to 2 years
Title
Change in systolic blood pressure from baseline to 12 months
Time Frame
Baseline to 1 year
Title
Change in serum LDL cholesterol from baseline to 12 months
Time Frame
Baseline to 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 40 years or older Singapore citizens or Permanent Residents Visiting the recruiting polyclinic at least twice during the last 1 year Individuals with a diagnosis of hypertension (systolic BP ≥ 140 mm Hg or diastolic BP ≥ 90 mm Hg on two or more prior visits; physician diagnosed hypertension, or on antihypertensive medications) and uncontrolled blood pressure (systolic BP ≥ 140 mm Hg or diastolic BP ≥ 90 mm Hg) Exclusion Criteria: Active systemic illness including fever, recent hospitalization (i.e. during last 4 months), Clinically unstable heart failure or advanced kidney disease {estimated CKD-Epi glomerular filtration rate (GFR) <40 ml/min/1.73m2 or nephrotic range proteinuria (i.e. 3g/d or more)}, Known liver disease, Pregnancy or breastfeeding Any other major debilitating disease or mental illness that precludes validity of informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr Tazeen Jafar, MD
Phone
+6566012582
Email
tazeen.jafar@duke-nus.edu.sg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr Tazeen Jafar, MD, MPH
Organizational Affiliation
Duke-NUS Graduate Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
SingHealth Polyclinics (SHP)
City
Singapore
ZIP/Postal Code
150167
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr Ngaip Chuan Tan
Email
tan.ngiap.chuan@singhealth.com.sg

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35696440
Citation
Jafar TH, Tan NC, Shirore RM, Allen JC, Finkelstein EA, Hwang SW, Koong AYL, Moey PKS, Kang GC, Goh CWT, Subramanian RC, Thiagarajah AG, Ramakrishnan C, Lim CW, Liu J; for SingHypertension Study Group. Integration of a multicomponent intervention for hypertension into primary healthcare services in Singapore-A cluster randomized controlled trial. PLoS Med. 2022 Jun 13;19(6):e1004026. doi: 10.1371/journal.pmed.1004026. eCollection 2022 Jun.
Results Reference
derived
PubMed Identifier
34301679
Citation
Porhcisaliyan VD, Wang Y, Tan NC, Jafar TH. Socioeconomic status and ethnic variation associated with type 2 diabetes mellitus in patients with uncontrolled hypertension in Singapore. BMJ Open Diabetes Res Care. 2021 Jul;9(1):e002064. doi: 10.1136/bmjdrc-2020-002064.
Results Reference
derived
PubMed Identifier
33468225
Citation
Allen JC Jr, Halaand B, Shirore RM, Jafar TH; for SingHypertension Study Group. Statistical analysis plan for management of hypertension and multiple risk factors to enhance cardiovascular health in Singapore: the SingHypertension pragmatic cluster randomized controlled trial. Trials. 2021 Jan 19;22(1):66. doi: 10.1186/s13063-020-05016-4. Erratum In: Trials. 2021 Feb 8;22(1):122.
Results Reference
derived
PubMed Identifier
29540213
Citation
Jafar TH, Tan NC, Allen JC, Finkelstein EA, Goh P, Moey P, Quah JHM, Hwang SW, Bahadin J, Thiagarajah AG, Chan J, Kang G, Koong A. Management of hypertension and multiple risk factors to enhance cardiovascular health in Singapore: The SingHypertension cluster randomized trial. Trials. 2018 Mar 14;19(1):180. doi: 10.1186/s13063-018-2559-x.
Results Reference
derived

Learn more about this trial

Management of Hypertension and Multiple Risk Factors to Enhance Cardiovascular Health

We'll reach out to this number within 24 hrs