- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05218304
Baromètre Santé Adulte 2021-2022
Baromètre Santé Adulte 2021-2022 in People Aged 18 to 64 in New Caledonia Using the WHO STEPwise Approach
In 2021-2022, Agence Sanitaire et Sociale Nouvelle Calédonie (ASSNC) is undertaking the "Baromètre Santé Adulte" for the third time. This study is carried out this year in collaboration with WHO and Institut Pasteur de Nouvelle Calédonie (IPNC).
The main objective of this investigation is to describe the current levels of chronic disease risk factors in the adult population of New Caledonia aged from 18 to 64 years old. This study will also help to estimate prevalence of certain diseases (diabetes, hypercholesterolemia, renal failure), seroprevalence of arboviruses (dengue fever, Zika, chikungunya and Ross River) malaria as well as the seroprevalence of SARS-CoV-2.
Repeated regularly, these surveys allow the ASS-NC to capitalize on population indicators, to compare them according to socio-demographic characteristics, to identify groups at risk, to provide changes in health behaviors and to strengthen analytical capacities in order to adapt the guidelines for public policies and prevention programs.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The "Barometre Santé Adulte" is an observational, descriptive and cross-sectional study whose data collection will take place in New Caledonia.
For this study the sampling is based on the 2019 population census, according to a 3-stage stratified sample design. In total, the main sample will consist of approximately 5,500 people (first phase) and the sub-sample will consist of 1,800 people (second phase).
The participation rate is estimated at 60%. Data collection will take place from February to May at the people's place drawn according to two steps:
- Firstly, investigators will carry out a questionnaire with the people who gave their informed consent as well as taking physical measurements: height, weight, abdominal circumference and blood pressure. In addition to the socio-demographic characteristics of the respondents, the questionnaire deals with several health topics: consumption of psychoactive substances, diet, physical activity, health status and access to care, screening, oral health, driving motor vehicle risk, sexual health, mental health, etc. The time taken to complete the questionnaire is estimated at one hour.
- Secondly, and for a sub-sample of 1,800 people, nurses will come back to the people's places who volunteer to take a venous blood test: blood sugar, total cholesterol, HbA1c, serum creatinine, CBC and serology of diseases transmitted by mosquitoes (dengue, chikungunya, Zika and Ross River, malaria).
All the data collected will be entered on a tablet in the eSTEPS application. The analysis of data (R Studio software) and the drafting of the report will be carried out by ASSNC staff. The first results are expected for the second half of 2022.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Nouméa, New Caledonia, 98800
- Agence Sanitaire et Sociale Nouvelle Calédonie
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Individuals informed of the conduct of the research and having given their written consent to participate in the study (questionnaire and taking physical measurements);
- Individuals between the ages of 18 and 64;
- Individuals residing in New Caledonia in so-called "ordinary" housing under their main residence at the last population census in 2019;
Exclusion Criteria:
- Pregnant or breastfeeding women;
- Tourists and transients staying in New Caledonia for less than 6 months at the time of the investigation;
- People who are not intellectually fit to answer the questionnaire;
- Persons subject to guardianship, curatorship or any other legal incapacity;
- For the second phase of the study will be excluded people describing a febrile syndrome;
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Sample
questionnaires physical measurements (height, weight, perimeter abdominal and blood pressure)
|
|
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Experimental: Sub-sample - blood test
questionnaires physical measurements (height, weight, perimeter abdominal and blood pressure) Blood samples
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A questionnaire, physical measurements (height, weight, perimeter abdominal and blood pressure) for all arm will be done, approximately 5400 people carried out by investigators.
Only 1800 will undergo blood samples carried out by nurses
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To know the prevalence of the main risk factors chronic diseases (obesity, diabetes, high blood pressure, high cholesterol and kidney failure) in the adult population of New Caledonia aged 18 to 64 using the WHO STEPS survey method.
Time Frame: Within a year after recruiting the participant
|
In order to measure the prevalence of the main risk factors chronic diseases, WHO STEPS method will be used.
This questionnaire is a 3 steps method, the first steps is a questionnaire mainly based on medical history and health behaviors.
The second steps is associated with taking physical measurements such as weight, height, blood pressure, waist size.
The last steps concerned only the experimental group "the sub-sample" for which some blood sample will be drawn out for the detection of elevated levels of blood glucose, HbA1c, total cholesterol and serum creatinine.
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Within a year after recruiting the participant
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health behaviors of the target population using the first step of the WHO STEPS survey method.
Time Frame: Within a year after recruiting the participant
|
To correlate health data and everyday behaviors of the target population in order to show a trend in causal effect, in order to have specific health indicators up to date
|
Within a year after recruiting the participant
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To calculate the cardiovascular risk of the New Caledonian population using the SCORE projet
Time Frame: Within a year after recruiting the participant
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To calculate the cardiovascular risk based on systolic blood pressure, sex, smoking status and cholesterol level.
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Within a year after recruiting the participant
|
|
Seroprevalence of infectious diseases
Time Frame: Within a year after recruiting the participant
|
To Determine the seroprevalence of dengue, Zika, chikungunya and Ross River arboviruses in New Caledonia, the seroprevalence against the malaria agent as well as the seroprevalence of SARS-CoV-2.
|
Within a year after recruiting the participant
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Metabolic Diseases
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Disease Attributes
- Arbovirus Infections
- Vector Borne Diseases
- Flavivirus Infections
- Flaviviridae Infections
- Lipid Metabolism Disorders
- Hyperlipidemias
- Dyslipidemias
- Hemorrhagic Fevers, Viral
- Severe Acute Respiratory Syndrome
- Chronic Disease
- Hypercholesterolemia
- Dengue
Other Study ID Numbers
- 2021-A01260-41
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- Statistical Analysis Plan (SAP)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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