The Nueva Ecija Cardiovascular Risk Experiment
NCT03512691 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5019
Last updated 2019-04-17
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
- Cardiovascular Diseases
- Cardiovascular Risk Factor
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
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