The Nueva Ecija Cardiovascular Risk Experiment

NCT03512691 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5019

Last updated 2019-04-17

No results posted yet for this study

Summary

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.

Conditions

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.

Sponsors & Collaborators

  • University of Lausanne

    collaborator OTHER
  • UPecon Foundation, Inc.

    lead OTHER

Principal Investigators

  • Joseph J Capuno, PhD · UPecon Foundation, Inc.

  • Aleli D Kraft, PhD · UPecon Foundation, Inc.

  • Owen O'Donnell, PhD · University of Lausanne

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-01-20
Primary Completion
2018-05-31
Completion
2021-12-31

Countries

  • Philippines

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03512691 on ClinicalTrials.gov