ClinicalTrials.gg
CompletedNCT05882682KenyaMPSUpdated May 31, 2023

Impact of Food-to-Food Fortified Cereal Products on Diet Quality in Eldoret, Kenya

An observational study in Vitamin A Deficiency and Iron-deficiency, sponsored by Purdue University. Completed at 1 site in Kenya. Open to participants aged 18 Months and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-05-31.

Sponsored by Purdue University · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
1,800
Ages
18 Months and older
Sex
All
01

Study summary

The overall hypotheses is that a product designed with optimized nutritional characteristics, based on consumer preferences and leveraging local nutrient dense ingredients, can successfully deliver nutrition through sustainable market-driven approaches.

The objectives of this study will be 1) to assess the nutritional adequacy of Kenyan households with children and 2) to determine the market potential of a locally sourced and manufactured, blended fortified, cereal-based product for the improvement of micronutrient deficiencies among children aged 24-60 months. This study will simulate a market study, the investigators conducted a product launch, determined market potential based on sales, evaluated marketing strategy to increase market share, and modeled the nutritional contribution of FtFF/traditionally fortified product for iron, zinc, and vitamin A. The investigators expect to provide a throughout evaluation of a business-driven strategy (for profit, social enterprise) as a sustainable tool to decrease micronutrient deficiencies.

Read the detailed description

Basic design:

Participants will be approached/recruited by research assistants on the ground at designated local markets. Potential participants will be consented if they agree to join the study at the time of recruitment. While attendance is not required by participants, product demonstrations will be conducted at the study sites, similar to a grocery store demonstration, to show how the instant flour is reconstituted. At the same time, consumers who are attending the demonstrations may be asked if they would participate in the study. Research assistants will read the consent form to the participants and ensure they understand it. Purdue investigator(s) (one or more - Torres-Aguilar, Rendall, Hamaker) will be present in Eldoret at all study phases involving consenting and data collection.

Products will be produced, distributed on a weekly basis to sites. The investigators plan on introducing the "new" product to consumers at random at in-store displays at individual locations for 2 weeks, and then continue to promote (advertise) and sell the placed product for a period of 8 weeks. The following schedules are proposed:

Weeks 1-2: Product demonstrations and sampling for consumers Weeks 3-5: Product sold at below market cost of other cereal flour products (as part of active promotion) Weeks 6-10: At one half of the locations, product sold at parity to other cereal products (with advertising but no additional promotion, i.e. discounts).

Data to be collected both from store managers and individual consumers. Enumerators will be trained and placed at each sales' location in the morning and evening to coincide with peak shopping times. They will be tasked with collecting a random sample of consumers who are purchasing cereals (1,200 total over 10 weeks). In this sample, both purchasers and non-purchasers of the FtFF fortified products will be identified and consented. Phone numbers will be collected and a follow up appointment/interview scheduled with half of them (600).

Enumerators will also coordinate the collection of data from point of sale managers:

  1. Total volume/units of FtFF fortified product sold
  2. Total volume/units cereal products sold
  3. Total value of FtFF fortified product sold
  4. TotaI value of cereal product sold
  5. Product comments from consumers (include any returns or complaints)
  6. Number of repeat purchasers

Follow up interviews with consumers will be conducted at a private location close to the centralized market sites or points of original purchase within 2 weeks. This is to enable follow up without inconveniencing participant.

02

Conditions studied

  • Vitamin A Deficiency
  • Iron-deficiency
03

In context

Vitamin A Deficiency

67 studies on the registry are indexed under Vitamin A Deficiency; 7 are open to participants now.

This study's enrollment of 1,800 is above the median of 258 across 17 observational studies indexed under Vitamin A Deficiency.

Browse Vitamin A Deficiency studies →

Lead sponsor

Purdue University is the lead sponsor of 175 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Months and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

This study will collect data about dietary habits for children and the household they lived. Adult caregivers will be approached and provided the relevant information.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults (>18 years of age), with child(ren) 5 years of age living in the household.

Exclusion criteria

Exclusion Criteria:

  • No children under 5 y of age living in the household.
  • Not a caregiver for the children in the household.
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
1,800 participants (actual)
Target follow-up
10 Weeks
Patient registry
Yes

Groups and cohorts

  • Consumers of cereal products

    Caregivers with children under 5 years of age who are consumer of cereal products in the Eldoret area.

06

What researchers measure

Primary outcomes

  1. Assessment of staple intake in urban Kenyan households and children

    A quantitative, modified food frequency questionnaire (FFQ) will be used to assess consumption of various starch rich staples (rice, corn, sorghum, millet, potatoes, cassava) and starch-rich processed foods (bread) for the whole household and children. The caregiver will provide information about the child's amount and frequency of consumption. This will be measured in g/day\*child. We will ask #times/week each staple was consumed as well as the average portion size consumed each time (g).

    Time frame: 10 weeks

  2. Assessment of the nutritional adequacy of urban Kenyan households and children

    Nutritional status of children in the household will be assessed using the Food Consumption Score Nutritional Quality Analysis (FCS-N) which was based on country-specific food groups. Food groups are orange fruits, orange vegetables, other fruits, eggs, dairy, organ meats, meat, fish, grains and legumes. Example of food items in the FCS-N assessment will be corroborated by a Kenyan maternal and child health expert. This will be measured in #times/week each food group was consumed.

    Time frame: 10 weeks

07

Study locations

1 site
  • University of Eldoret
    Eldoret, Uasin Gishu, Kenya
08

References and documents

Individual participant data

Plan to share: No — No PI was collected. There is not a plan to share participant information.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Oct 2022 to primary completion in Dec 2022, 1 month.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 14, 2023
First posted
May 31, 2023
StartActual
Oct 20, 2022
Primary completionActual
Dec 12, 2022
CompletionActual
Dec 30, 2022
Last update
May 31, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 31, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05882682
Lead sponsor
Purdue University
Responsible party
Bruce R. Hamaker (Principal Investigator / Distinguished professor, Purdue University) — Principal investigator
First posted
May 31, 2023
Start date
Oct 20, 2022
Primary completion
Dec 12, 2022
Completion
Dec 30, 2022
Last update
May 31, 2023

Study contacts

Bruce R Hamaker
principal investigator · Purdue University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2023. You cannot join it, but the record below documents what was studied.

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Discussion

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