The Nueva Ecija Cardiovascular Risk Experiment

Overview

This study seeks to assess how beliefs about health risks, specifically the risk of cardiovascular disease (CVD), affect health lifestyles and the demand for preventive care in a low-income setting. It also aims to establish the effectiveness of the Package of Essential Noncommunicable Disease Interventions in the Philippines (PhilPEN) in delivering primary prevention of CVD. To meet these objectives, the study is designed as a randomized parallel experiment with two separate, non-overlapping treatment groups and one control group. The experiment will be implemented in Nueva Ecija province, Philippines.

Full Title of Study: “The Nueva Ecija Cardiovascular Risk Experiment: An Evaluation of the Impact of Risk Information and Screening on Primary Prevention of Cardiovascular Disease”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Health Services Research
    • Masking: Single (Participant)
  • Study Primary Completion Date: May 31, 2018

Detailed Description

This study seeks to assess how beliefs about health risks, specifically the risk of cardiovascular disease (CVD), affect health lifestyles and the demand for preventive care in a low-income setting. It also aims to establish the effectiveness of the Package of Essential Noncommunicable Disease Interventions in the Philippines (PhilPEN) in delivering primary prevention of CVD.To realize the first objective, the investigators will measure the accuracy of beliefs about exposure to CVD risk and, subsequently, randomly provide information on personal CVD risk based on measured risk factors. This will allow assessment of the extent to which biased beliefs constrain demand for primary prevention and sustain unhealthy lifestyles. In addition, the investigators will test whether beliefs about susceptibility to CVD are responsive to the receipt of information on personal risk, and whether health behaviors and the demand for CVD screening and medication are affected by any revision of beliefs. To meet the second objective the investigators will randomly encourage uptake of the PhilPEN program's risk screening by offering entry to a money prize lottery conditional on attending a health clinic where the program operates. The induced random variation in clinic attendance will be used to estimate the program's impact on exposure to risk factors, medication of hypertension, the predicted risk of CVD and awareness of this risk. Meeting both objectives will allow the investigators to distinguish between scenarios. One is that PhilPEN is effective in preventing CVD of patients who access the program but its impact on population health is muted because poor information on susceptibility to CVD reduces the demand for primary prevention. Another is that even if improved information is effective in raising this demand, this will have little impact on population health through PhilPEN because of deficiencies in the operation of the program in health facilities. Within the Nueva Ecija province, the investigators will randomly sample barangays (N=304), subsequently households (n=5019) and, finally, one person aged 40-70 within each household. At the barangay level, the investigators will randomly allocate to a treatment group receiving the lottery incentive to attend a health clinic (n=2261), another treatment group receiving information on personal CVD risk (n=497) and a control group (n=2261). A baseline survey (January-April 2018) will record data on initial health, health behavior, health knowledge, risk perceptions, risk attitudes, time preferences, health care utilization and expenditure and socioeconomic characteristics, and deliver the treatments. A follow-up survey 9-12 months later will record outcomes.

Interventions

  • Behavioral: Information on CVD Risk
    • Respondents will be provided three types of information on CVD risks: a CVD base rate, a personalized CVD risk and an optimal CVD risk. The CVD base rate will be predicted from the respondent’s age and sex only. After reporting their own chance of having a heart attack or stroke within ten years, the respondents in the treatment group will be told the risk for someone with the same age, sex, smoking status, body mass index (BMI) and blood pressure as them. Finally, a treatment group respondent will receive information on what the 10-year CVD risk would be for someone of the same age and gender who did not smoke, and had normal blood pressure and BMI.
  • Behavioral: Lottery Incentive
    • Respondents will simply be told that they can enter a lottery if they go to the specified clinic for a checkup. The health facilities will be told to conduct an assessment deemed appropriate for any particular patient that requests to be issued with a lottery ticket. No instructions will be given that the facilities should follow the PhilPEN protocol. We will evaluate whether they do implement the protocol for patients who qualify (by age if nothing else) for full risk screening.

Arms, Groups and Cohorts

  • Experimental: Information on CVD risk
    • Respondents will receive information on the predicted probability of having a heart attack or stroke within 10 years. The predictions will be obtained from the Globorisk tool (www.globorisk.org). All information will be provided within a risk perceptions module of the baseline survey. Only this module will differ across the two treatment groups (information and lottery) and the control group. Information obtained from earlier modules will be retrieved automatically and used to make predictions of CVD risk consistent with the risk factor profile of the respondent.
  • Experimental: Lottery Incentive
    • Respondents will be offered a ticket for a lottery with a money prize on condition that they visit a specific public health clinic for a checkup. There will be one prize per barangay giving each respondent a one in ten chance of winning P5000 (US$100). The prize is equivalent to approximately 14 days earnings at the regional minimum wage.
  • No Intervention: Control
    • No intervention will be introduced to the participants in this arm.

Clinical Trial Outcome Measures

Primary Measures

  • Mean 10-year risk of CVD event (heart attack/stroke)
    • Time Frame: 6-9 months
    • Predicted probability of having a heart attack or stroke within 10 years obtained from office version of Globorisk (www.globorisk.org) based on age, sex, systolic blood pressure, body mass index (BMI) and smoking status recorded in end-point survey. Group mean of predictions will be calculated.

Secondary Measures

  • Proportion with 10-year CVD risk ≥ 10%
    • Time Frame: 6-9 months
    • Predicted risk obtained from Globorisk as for primary outcome. If power permits, will also estimate effects on proportion with CVD risk>20% and >30%.
  • Mean systolic blood pressure (SBP)
    • Time Frame: 6-9 months
    • Predicted CVD risk is function of blood pressure, BMI and smoking. We will also estimate effects on these risk factors separately. Mean of last two SBP measures on single visit. BP measured using electronic (OMRON) wrap cuff monitor.
  • Proportion with elevated blood pressure (systolic ≥140)
    • Time Frame: 6-9 months
    • Predicted CVD risk is function of blood pressure, BMI and smoking. We will also estimate effects on these risk factors separately. Mean of last two SBP measures on single visit. BP measured using electronic (OMRON) wrap cuff monitor.
  • Mean BMI
    • Time Frame: 6-9 months
    • Predicted CVD risk is function of blood pressure, BMI and smoking. We will also estimate effects on these risk factors separately. Height and weight measured using standardized instruments.
  • Proportion overweight/obese (BMI>25)
    • Time Frame: 6-9 months
    • Predicted CVD risk is function of blood pressure, BMI and smoking. We will also estimate effects on these risk factors separately. Height and weight measured using standardized instruments.
  • Proportion currently smoking
    • Time Frame: 6-9 months
    • Predicted CVD risk is function of blood pressure, BMI and smoking. We will also estimate effects on these risk factors separately.
  • Mean waist circumference
    • Time Frame: 6-9 months
    • Globorisk predicted 10-year CVD risk is not a function of central adiposity, but this is measured as part of PhilPEN risk assessment. Weight circumference will be measured followed a standardized procedure.
  • Proportion with waist circumference ≥ 90cm (men) / 80cm (women).
    • Time Frame: 6-9 months
    • Globorisk predicted 10-year CVD risk is not a function of central adiposity, but this is measured as part of PhilPEN risk assessment. Weight circumference will be measured followed a standardized procedure.
  • Proportion with undiagnosed hypertension
    • Time Frame: 6-9 months
    • A measure of diagnosis and medication of hypertension. Numerator = systolic/diastolic BP ≥ 140/90 + not diagnosed with hypertension. Denominator = all respondents.
  • Proportion taking antihypertensive medication in the last 2 weeks.
    • Time Frame: 6-9 months
    • A measure of diagnosis and medication of hypertension. Numerator = systolic/diastolic BP ≥ 140/90 + not diagnosed with hypertension. Denominator = all respondents.
  • Alcohol consumption
    • Time Frame: 6-9 months
    • A measure of health behavior consistent with those of World Health Organization (WHO) STEPS.
  • Diet (intake of fruits, vegetables and salty foods)
    • Time Frame: 6-9 months
    • A measure of health behavior consistent with those of WHO STEPS.
  • Exercise
    • Time Frame: 6-9 months
    • A measure of health behavior consistent with those of WHO STEPS.
  • Knowledge of CVD and diabetes risk factors
    • Time Frame: 6-9 months
    • Knowledge of CVD and diabetes risk factors assessed using questions adapted from previously fielded instruments.

Participating in This Clinical Trial

Inclusion Criteria

  • Individuals aged 40-70 years old – Residents of Nueva Ecija province – Those that have been diagnosed with hypertension but are not currently (past two weeks) taking antihypertensives Exclusion Criteria:

  • Individuals aged below 40 years old or above 70 years old – Individuals who report they have been diagnosed as having heart disease or diabetes, or who report that they have had a heart attack or a stroke – Those currently (past 2 weeks) taking medication for hypertension or for diabetes – Those who have some medical problems that prevents measurement of blood pressure or BMI

Gender Eligibility: All

Minimum Age: 40 Years

Maximum Age: 70 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • UPecon Foundation, Inc.
  • Collaborator
    • University of Lausanne
  • Provider of Information About this Clinical Study
    • Principal Investigator: Joseph J. Capuno, Principal Investigator – UPecon Foundation, Inc.
  • Overall Official(s)
    • Joseph J Capuno, PhD, Principal Investigator, UPecon Foundation, Inc.
    • Aleli D Kraft, PhD, Principal Investigator, UPecon Foundation, Inc.
    • Owen O’Donnell, PhD, Principal Investigator, University of Lausanne
  • Overall Contact(s)
    • Joseph J Capuno, PhD, 6329205465, jjcapuno@up.edu.ph

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