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Completed

NCT Number: NCT01614483

Efficacy of Yellow Cassava to Improve Vitamin A Status of Kenyan School Children

The overall aim of the project is to provide proof-of-principle that biofortification of cassava with vitamin A is a viable strategy to improve vitamin A status of deficient populations.

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Key information

Age range

61 month–13 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kibwezi District

Kibwezi, Eastern Kenya, Kenya

About this study

Rationale: Vitamin A deficiency is still common in developing countries and has been proven difficult to combat. A promising approach is to replace common crops with varieties that are naturally richer in vitamin A, which is referred to as biofortification. For cassava, yellow β-carotene rich varieties have recently been introduced in Kenya, and these varieties are now ready to be tested for their efficacy to improve vitamin A status in humans.

Objective: The primary objective is to measure the effect of daily consumption of provitamin A biofortified cassava (providing 50% of the age-specific RDA) on vitamin A status in children aged 5-13 years with mild to moderate vitamin A deficiency in Kenya. To determine the bioefficacy of provitamin A carotenoids from biofortified cassava relative to that of a daily B-carotene supplement (comparison with positive control group). Secondary objectives are: 1) to measure the effect of the intervention on immune function indicators and morbidity; 2) to determine to what degree the serum retinol response to the intervention depends on serum concentrations of retinol and zinc at baseline; 3) to determine the effect of the intervention on functional indicators such as dark adaptation capacity, gut integrity, hematology indicators and thyroid status; 4) to determine the mediating effect of SNP's in the BCMO1 gene on treatment outcome.

Study design & Study population : In this randomized controlled trial, school children aged 5-13 years living in the Kibwezi area, Kenya. Children will be selected from three (or four) primary schools in the area that have been pre-selected based on the prevalence of vitamin A deficiency, location and willingness to participate.

Intervention: After screening for eligibility and a 2-week run-in period (n=360) Children will be randomly allocated to three different treatments: 1) 400 g of yellow cassava providing ~50% of the RDA for vitamin A; and a placebo capsule; 2) 400 g of white cassava; and a placebo capsule; 3) 400 g of white cassava and a capsule containing 100 RAE of all-trans β-carotene.

Main study parameters/endpoints: The main outcome measure will be differences in serum retinol concentrations between groups. Other outcome measures include other vitamin A status indicators (β-carotene, retinol binding protein, transthyretin), immune function indicators, dark adaptation, iron status indicators, anthropometrics, gut integrity, and thyroid function.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Low vitamin A status (retinol binding protein (RBP) at the lowest end of the distribution will be included in the study)

Exclusion criteria

  • History or signs of infectious or systemic diseases (e.g. tuberculosis, sickle cell anaemia)
  • Anaemia, malaria or acute inflammation at the day of baseline measurements

Treatment and study plan

Yellow cassava

Other

Daily provision of 375 g boiled yellow cassava for 18 weeks, 6 days/week Daily provision of placebo capsule for 18 weeks, 6 days/week

White cassava

Other

Daily provision of 375 g boiled white cassava for 18 weeks, 6 days/ week Daily provision of placebo capsule for 18 weeks, 6 days/ week

Primary outcomes

  1. Change in serum retinol concentration

    Time frame: Baseline, end of study (4 months)

Secondary outcomes

  1. Immune function indicators

    Time frame: End of study (4 months)

    neopterin, IL-2, IL4, IL10, IL13, TNF-a, IFN-γ, TGF-β in serum; IgA in saliva

  2. Bioefficacy

    Time frame: Baseline, end of study (4 months)

    Comparison of change in serum retinol between yellow cassava group and positive control (B-carotene supplement group)

  3. Functional indicators

    Time frame: End of study (4 months)

    Gut integrity, dark adaptation, morbidity

  4. Thyroid function

    Time frame: End of study (4 months

    Serum Tg, TSH

  5. Effect modification

    Time frame: Baseline

    Serum zinc, serum retinol, iron status, polymorphisms

  6. Anemia

    Time frame: End of study (4 months)

    Hemoglobin

Sponsors and collaborators

Lead sponsor

Wageningen University

Other

Collaborators

  • European Commission
  • University of Nairobi

Registry information

Official study title

Efficacy of Yellow Cassava to Improve Vitamin A Status of Mildly Deficient Primary School Children in Kenya: a Randomized Controlled Trial

Acronym: CASSAVITA

Important dates

Study start
2012
Primary completion
2012
Study completion
2012
First posted
Jun 8, 2012
Registry last updated
Nov 21, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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