Dietary Practices and Metabolic Syndrome in the Young Adult Population of Rwanda (NutriTransit)

February 6, 2024 updated by: University Ghent

Evaluation of Dietary Practices and Assessment of Nutritional Status and Associated Risk Factors for Metabolic Syndrome in the Young Adult Population of Rwanda

Policy makers in Rwanda have recently highlighted the importance of promoting healthy diets and lifestyle in response to rapidly increasing rates of obesity. This project will provide evidence on shifts in diet and nutritional status in urban dwellers as compared to the traditional diet and lifestyle in rural areas as a basis for a targeted public health policy for Rwanda.

Study Overview

Detailed Description

Adequate diet has been known for many years to be a major lever to significantly decrease the risk for non-communicable diseases (NCD). However, mainly due to urbanization and improved economic status in low and middle income countries (LMICs), the traditional largely plant-based diets are being replaced by more energy-dense and nutrient poor diets, incorporating more animal foods and processed foods and fat, and with a decrease in consumption of fruits and vegetables and other plant based foods. This diet change together with a sedentary lifestyle are typical phenomena in LMICs that are driving the so-called nutrition transition that is typically accompanied by an increase in obesity and in NCD like metabolic syndrome, diabetes, cardiovascular diseases and cancer. In Rwanda, NCD lead to 36% of total deaths. Cancers, diabetes, cardiovascular diseases, and chronic respiratory diseases account for 82% of NCD deaths. The major risk factor is the raised blood pressure (34.4%) and the probability of dying between ages 30 and 70 years from those four main NCD is estimated to 19%.

The Government of Rwanda has installed an operational NCD unit in the Ministry of Health with a view to developing preventive strategies vis-à-vis the nutrition transition process in the country. It has been shown already that there is a need for adopting dietary behaviour change to prevent the epidemic of chronic diseases.

The aim of this PhD work is to contribute in generating evidence needed to develop targeted prevention strategies for NCD in a broader framework of informed health policy making in Rwanda.

Specific objectives:

  1. To identify the changes in eating habits of different socio- economic subgroups in adults living in Kigali, in comparison to their peers in rural areas;
  2. To assess nutritional status and body composition using several methods (BMI, skinfold thicknesses, sitting height and body build, fat and fat free mass), with the ultimate objective to establish population-body composition-derived BMI cut-offs for overweight and obesity in this population;
  3. To assess and compare the prevalence of common risk factors for non-communicable disease (high BMI, low fruit and vegetable consumption, low physical activity and high blood pressure) between rural and urban areas;
  4. To evaluate people's nutrition knowledge, aptitude and capacity (KAP), perception of obesity and normal weight and food insecurity levels as risks factors for adherence to healthy dietary practices and life style;
  5. To generate information to be used by governments to improve dietary habits and physical activity through targeted interventions.

The data collected in a cross sectional study design. Validated questionnaires will be used to get information on socio-economic characteristics, dietary practices, physical activity, other lifestyle factors and psycho-social and emotional indicators.

Study Type

Observational

Enrollment (Actual)

1247

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Kigali, Rwanda
        • University of Rwanda

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Participants will be selected randomly from the general population. Eligible subjects who agree to participate (informed consent) will be enrolled in the study.

Description

Inclusion Criteria:

  • Permanent residence of the selected urban or rural villages
  • Holding a valid health insurance card
  • Aged between 18 and 35 years
  • Signing informed consent form
  • Registration in city demographic system, since study participants will be selected from population registration cards at village level,
  • Accept enumerators for home visit and data collection
  • Accept to visit the laboratory for blood sample collection,
  • Not suffering from any chronic disease such as VIH/ AIDS, diabetes, asthma, etc.

Exclusion Criteria:

  • Lactating, pregnant, and recently delivering (less than six month-postpartum) women
  • Physical disabilities that can prevent participants from working
  • Mental disability such as clinically diagnosed depression, anxiety disorders, eating disorders and addictive behaviors.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Urban
Young adults living in urban communities of Rwanda
Data collected using food frequency questionnaire
Data collected on nutritional status, biochemical indicators and other risk factors associated with metabolic syndrome
Rural
Young adults living in rural communities of Rwanda
Data collected using food frequency questionnaire
Data collected on nutritional status, biochemical indicators and other risk factors associated with metabolic syndrome

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of the different dietary patterns
Time Frame: Through study completion (an average of 6 months)
Dietary patterns will be identified using exploratory factor analysis on the food groups collected using the semi-quantitative Food Frequency Questionnaire. The dietary pattern identified will differ from plant_based diet and legume_based diet to western diet.
Through study completion (an average of 6 months)
Prevalence of large waist circumference
Time Frame: Through study completion (an average of 6 months)
Large waist circumference [> 89 centimeters for women and >102 centimeters for men]
Through study completion (an average of 6 months)
Prevalence of high triglyceride concentrations
Time Frame: Through study completion (an average of 6 months)
High triglyceride level [>150 milligrams per deciliter (mg/dL)]
Through study completion (an average of 6 months)
Prevalence of high-density lipoprotein (HDL) cholesterol
Time Frame: Through study completion (an average of 6 months)
Reduced high-density lipoprotein (HDL) cholesterol [< 40 mg/dL in men or < 50 mg/dL in women]
Through study completion (an average of 6 months)
Prevalence of high blood pressure
Time Frame: Through study completion (an average of 6 months)
Increased blood pressure [> 130/85 mm Hg]
Through study completion (an average of 6 months)
Prevalence of high levels of fasting blood sugar
Time Frame: Through study completion (an average of 6 months)
Elevated fasting blood sugar [>100 mg/dL]
Through study completion (an average of 6 months)
Prevalence of participants with nutrition knowledge
Time Frame: Through study completion (an average of 6 months)
Nutritional knowledge of macronutrients, micronutrients, water intake, diet and disease will be collected using a multiple choice answers. Each question had one mark for every correct response chosen. Using a marking scheme for nutritional knowledge test the scores were rated on score percentages using eight cut off points, with scores less than 20% indicating a bad nutritional knowledge, 50-59% satisfactory and Excellent for those scoring 80% and more.
Through study completion (an average of 6 months)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of Food Insecure Households
Time Frame: Through study completion (an average of 6 months)

The Household Food Insecurity Access (HFIA) Score is a continuous measure of the degree of food insecurity in the household and is based on a set of questions that encompass three domains of food insecurity: (1) anxiety and uncertainty about the household food supply; (2) insufficient quality; and (3) insufficient food intake and its physical consequences (Coates et al. 2007).

Each household receives a score from 0-27 based on a simple sum of the frequency of occurrence of each food insecurity condition, where 'never' = 0 points, 'rarely' = 1 point, 'sometimes' = 2 points, and 'often' = 3 points. The higher the score, the higher the degree of household food insecurity experienced in the previous four weeks.

Through study completion (an average of 6 months)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hilda Vasanthakaalam, PhD, University of Rwanda
  • Principal Investigator: Jerome Some, Md. PhD, Institut de Recherche en Sciences de la Sante, Ouagadougou, Burkina Faso
  • Principal Investigator: Stefaan De Henauw, Md. PhD, University of Ghent
  • Principal Investigator: Souheila Abbeddou, MSc. PhD, University of Ghent

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2021

Primary Completion (Actual)

December 31, 2023

Study Completion (Actual)

December 31, 2023

Study Registration Dates

First Submitted

November 27, 2019

First Submitted That Met QC Criteria

December 16, 2019

First Posted (Actual)

December 19, 2019

Study Record Updates

Last Update Posted (Estimated)

February 7, 2024

Last Update Submitted That Met QC Criteria

February 6, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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