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Diet; DeficiencyANNCT06175130

Cross-sectional Dietary Intake Survey on Ivorian School-Aged Children and Women of Reproductive Age

An observational study of Diet; Deficiency, run by FrieslandCampina at 1 site in Netherlands.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

A cross-sectional dietary intake study was conducted with 423 Ivorian school aged children (SAC, 6-12 years) and 423 women of reproductive age (WRA, 15-49 years) from four cities, recruited by two-stage random sampling. Read more about this study

Who is it for?
Ages 6 to 50 yearsHealthy volunteers can take part
Conditions the study is for
Diet; Deficiency
How many people
846 participants
Where
1 siteNetherlands
Study dates
1 Feb 2021to 28 Feb 2021
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 50 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Study population: healthy children and women living in the cities of Ivory Coast

Who may be able to join

  • healthy

Who cannot join

  • illness or disease

Trial locations and contacts

1 site in 1 country.

Netherlands1 site
  • FrieslandCampina Research and Development

    Wageningen, 6708 WH

Other trials in Netherlands

About this study

Official title: Cross-sectional Dietary Intake Survey on Ivorian School-aged Children (6-12 yo) and Women of Reproductive Age (15-50 yo)

A cross-sectional dietary intake study was conducted with 423 Ivorian school aged children (SAC, 6-12 years) and 423 women of reproductive age (WRA, 15-49 years) from four cities, recruited by two-stage random sampling.

Read the detailed description

A cross-sectional dietary intake study was conducted with 423 Ivorian school aged children (SAC, 6-12 years) and 423 women of reproductive age (WRA, 15-49 years) from four cities, recruited by two-stage random sampling. Dietary intake data were collected by multiple pass 24-hour recall. For a sub-sample (10% subjects) two-day non-consecutive multiple pass 24-hour recall was collected.

Keywords
Nutrient Inadequacy, Dietary Patterns, Food Intake
Medical subject headings
Malnutrition

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06175130
Study groupRoleWhat they receive
Healthy children (6-12 years)Healthy children (6-12 years), no illness or disease
Healthy Women of reproductive age (15-50 years)Healthy Women of reproductive age (15-50 years), no illness or disease

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mean usual nutrient intake per day

    Mean usual nutrient intake of iron (mg), zinc (mg), vitamin A (RAE), calcium(mg), vitamin B1 (g), B2 (mg), B3 (mg), B6 (mg), B9 (ug), B12 (ug) and vitamin D (ug DFE) will be calculated based on food intake per person per day conversion to usual nutrient intakes per person per day using food composition tables.

    Measured: Standard multiple pass 24-hour recall

Secondary outcomes (2)
  1. Nutritional status (Prevalence of stunting, underweight, overweight and obesity)

    Height and weight were measured using standardized scales and height boards. Calculations were made comparing the individual's weight, height and age in some cases to define nutritional status indicators. Cut-offs used were defined by World Health Organization (WHO) Anthro Plus Software (version 1.0.4) for children and using WHO cut-off values for adults. Underweight (<18.5 kg/m2), normal (18.5-24.9 kg/m2), overweight (25-29.9 kg/m2) and obese (>30 kg/m2).

    Measured: on the spot measurement

  2. Food intake per day per person

    Food item and food group intake will be calculated based on classification of foods consumed into food groups

    Measured: Standard multiple pass 24-hour recall

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Dec 2023
  2. Study start1 Feb 2021
  3. Primary completion28 Feb 2021
  4. Study completion28 Feb 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
846 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06175130
Sponsor's protocol ID
AfricaNutrition
Acronym
AN
Status last verified
Dec 2023
First submitted
28 Nov 2023
Last updated
18 Dec 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The individual participant data will not be shared

Publications

  • Ayling K, Maasen K, de Jonge M, Konan AG, Tiahou G, Gbane M, Bovee-Oudenhoven I, Melse-Boonstra A, Talsma EF. Dietary Patterns and Nutritional Status of Urban School-Children and Adult Females of Reproductive Age in Cote d'Ivoire. Curr Dev Nutr. 2026 Jun 30;10(8):109419. doi: 10.1016/j.cdnut.2026.109419. eCollection 2026 Aug.

    PubMed 42571302
  • Ayling K, Talsma EF, Konan AG, Tiahou G, Gbane M, Bovee-Oudenhoven I, Melse-Boonstra A. Assuming the "Best-Fit" Shape of the Usual Nutrient Intake Distribution (with nutriR) Does Not Affect Prevalence Estimates of Nutrient Intake Inadequacy: Results from a Dietary Intake Survey in Ivorian School-Age Children. J Nutr. 2025 Jul;155(7):2449-2458. doi: 10.1016/j.tjnut.2025.05.023. Epub 2025 May 23.

    PubMed 40414299

Questions about this trial

What is this clinical trial studying?

An observational study of Diet; Deficiency, run by FrieslandCampina at 1 site in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Dec 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mean usual nutrient intake per day (time frame: Standard multiple pass 24-hour recall). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06175130, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Dec 2023.

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