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Efficacy of Caterpillar Cereal for Complementary Feeding in the Democratic Republic of Congo

A Novel Sustainable Complementary Feeding Product for Infants and Young Children in the Democratic Republic of Congo: Caterpillar Cereal

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01282788
Acronym
CAT02
Enrollment
222
Registered
2011-01-25
Start date
2011-01-31
Completion date
2012-12-31
Last updated
2013-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infectious Diseases Morbidity, Iron Deficiency Anemia, Malnutrition, Neurodevelopmental Impairment, Stunting of Growth

Keywords

infant nutrition, complementary feeding, malnutrition, stunting of growth

Brief summary

Two in every three infants in rural areas of the Democratic Republic of Congo (DRC) suffer from stunting of linear growth by 12 months of age. Stunting presumably results from breast milk supplementation after 6 months of age with complementary foods (CF) that provide inadequate protein and micro-nutrients. Although supplementation with selected micro-nutrients may avoid certain deficiency states, CF with animal source foods may be necessary to avoid stunting. Meat is not readily available in many Central African countries. However caterpillars, which are locally available and abundant, are a common staple in adult diets and may be a suitable substitute for animal source proteins in CF. The investigators developed a cereal made from dried caterpillars that has a nutrient content that appears to be ideal for CF and demonstrated maternal and infant acceptability. This study will investigate the efficacy in prevention of stunting of growth resulting from inadequate complementary foods. A sub-study will evaluate the biologic effects of the caterpillar cereal to determine whether caterpillar cereal prevents iron deficiency anemia, reduces the incidence of neurodevelopmental impairment or infectious diseases.

Detailed description

A randomized, controlled trial will be conducted in the Equateur Province. The study will be a cluster randomized, non-masked controlled trial of a daily intake of caterpillar cereal (Cereal Arm) versus the usual diet provided by the family (Traditional Diet Arm) from 6 to18 months of age. Eight communities (clusters) will be randomized to either the Cereal Arm or the Traditional Diet Arm of the study. A community will be comprised of approximately 10 to 12 rural villages served by one Health Center. Each Cereal community will be paired with a Traditional Diet community. Educational Information All participants will be provided with general education that will include: 1) critical messages about infant feeding and 2) instruction about hand hygiene and food preparation. The primary educators will be the Community Coordinators (CCs; specially-trained research nurses) working with the Health Center nurses. Messages will be delivered and reinforced with pictorial aids. Mothers in both arms will receive three repetitive messages to reinforce selected features of World Health Organization (WHO) recommendations for complementary feeding: 1. Feed thickened gruel or cereals every day 2. Feed infant/toddler at least 3 times a day 3. Maximize local food diversity Cereal Arm All infants in communities randomized to the Cereal Arm will receive once-daily servings of caterpillar cereal (30 g from 6-12 months of ages and 45 g from 12-18 months of ages). Study food will be delivered to homes weekly by CCs, who will also observe feedings of the cereal during the home visit. Feedings will be observed 3x/week for the first 3 weeks after enrollment, then 1x/week until 18 months of age. Parents and other care providers will receive specific instructions about cereal preparation and general education about feeding practices, food preparation and hygiene. This information will be reinforced during weekly visits. Traditional Diet Arm Infants in communities randomized to the Traditional Diet Arm will not receive food supplements. Parents and other care providers in this arm of the study will receive general education about feeding practices, food preparation and hygiene, with weekly reinforcement. Study Population A total of 220 infants (approximately 27 from each community; 110 infants in each arm) will be enrolled in the study. Records of all births within study communities will be obtained from local Health Center records. When infants reach 5 months of age, caregivers of randomly selected infants will be approached by CCs to seek consent for participation in this study. They will be supported by the Provincial Coordinator (the physician who oversees community-based studies conducted by the Kinshasa School of Public Health-University of North Carolina Partnership) who will hold group information meetings to introduce the study to community leaders.

Interventions

DIETARY_SUPPLEMENTCaterpillar Cereal

Infants will receive once-daily servings of caterpillar cereal (30 g from 6-12 months of ages and 45 g from 12-18 months of ages). Study food will be delivered to homes weekly by Community Coordinators, who will also observe feedings of the cereal during the home visit. Feedings will be observed 3x/week for the first 3 weeks after enrollment, then 1x/week until 18 months of age. Parents and other care providers will receive specific instructions about cereal preparation and general education about feeding practices, food preparation and hygiene. This information will be reinforced during weekly visits.

Sponsors

Kinshasa School of Public Health
CollaboratorOTHER
University of California, Davis
CollaboratorOTHER
Bill and Melinda Gates Foundation
CollaboratorOTHER
Thrasher Research Fund
CollaboratorOTHER
University of North Carolina, Chapel Hill
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Months to 18 Months
Healthy volunteers
Yes

Inclusion criteria

* Infants born in study communities who will reach 6 months of age during the six month period after initiation of the study

Exclusion criteria

* Infants likely to receive free or subsidized complementary foods (or infant formula) * Families likely to relocate during the study period * Infants with known congenital anomaly * Infants of multiple birth * Infants with neurological deficit apparent at the time of enrollment

Design outcomes

Primary

MeasureTime frameDescription
Incidence of Stunting of Linear Growth18 months of ageStunting of linear growth will be defined as a height-for-age Z score less than 2 using WHO standards.

Secondary

MeasureTime frameDescription
Incidence of wasting18 months of ageWasting will be defined as weight-for-age Z score less than 2 using the WHO growth standards.
Developmental Outcome18 months of ageThe Ages and Stages Questionnaire and the Bayley Scale of Infant Development II will be used to determine developmental outcome at 18 months of age.
Infectious Disease Morbidity6-18 monthsInfectious morbidities will be identified during weekly interviews of mothers by study personnel.
Rate of Head Growth18 months of ageHead circumference will be measured at enrollment (6 months of age) and conclusion of the study (18 months of age).
Compliance6-18 monthsCompliance with study protocol will be assessed by study personnel through interviewers with the mothers, direct observation, and recovery of unused cereal.
Iron Deficiency Anemia18 monthsWe will measure serum markers of iron deficiency, including hemoglobin levels, ferritin and soluble transferrin receptor.
All Cause Mortality6-18 monthsDeaths will be reported to study personnel by family members or local health officials.

Countries

Republic of the Congo

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026