ClinicalTrials.gg
CompletedNCT01282788CAT02Updated Dec 9, 2013

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

An interventional study of Caterpillar Cereal in Malnutrition, Stunting of Growth and Iron Deficiency Anemia, sponsored by University of North Carolina, Chapel Hill. Completed at 1 site in Congo. Open to participants aged 6 Months to 18 Months, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-12-09.

Sponsored by University of North Carolina, Chapel Hill · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
222
Allocation
Randomized
Ages
6 Months to 18 Months
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

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

Keywords

  • infant nutrition
  • complementary feeding
  • malnutrition
  • stunting of growth
03

In context

Malnutrition

1,277 studies on the registry are indexed under Malnutrition; 230 are open to participants now.

This study's enrollment of 222 is above the median of 118 across 843 interventional studies indexed under Malnutrition.

Browse Malnutrition studies →

Lead sponsor

University of North Carolina, Chapel Hill is the lead sponsor of 1,372 studies on the registry; 133 are open to participants now.

Of its 161 completed or terminated interventional studies of FDA-regulated products, 139 (86%) have results posted.

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

04

Who can participate

Ages eligible
6 Months to 18 Months
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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

Exclusion criteria

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
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
222 participants (actual)

Study arms

  • No intervention
    Traditional Diet

    Infants in communities randomized to the traditional diet arm will not receive food supplements.

  • Experimental
    Cereal

    All infants in communities randomized to the Cereal Arm will receive caterpillar cereal from 6-18 months of age.

    Dietary Supplement: Caterpillar Cereal

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.

06

What researchers measure

Primary outcomes

  1. Incidence of Stunting of Linear Growth

    Stunting of linear growth will be defined as a height-for-age Z score less than 2 using WHO standards.

    Time frame: 18 months of age

Secondary outcomes

  1. Rate of Head Growth

    Head circumference will be measured at enrollment (6 months of age) and conclusion of the study (18 months of age).

    Time frame: 18 months of age

  2. Incidence of wasting

    Wasting will be defined as weight-for-age Z score less than 2 using the WHO growth standards.

    Time frame: 18 months of age

  3. Developmental Outcome

    The Ages and Stages Questionnaire and the Bayley Scale of Infant Development II will be used to determine developmental outcome at 18 months of age.

    Time frame: 18 months of age

  4. Infectious Disease Morbidity

    Infectious morbidities will be identified during weekly interviews of mothers by study personnel.

    Time frame: 6-18 months

  5. All Cause Mortality

    Deaths will be reported to study personnel by family members or local health officials.

    Time frame: 6-18 months

  6. Compliance

    Compliance with study protocol will be assessed by study personnel through interviewers with the mothers, direct observation, and recovery of unused cereal.

    Time frame: 6-18 months

  7. Iron Deficiency Anemia

    We will measure serum markers of iron deficiency, including hemoglobin levels, ferritin and soluble transferrin receptor.

    Time frame: 18 months

07

Study locations

1 site
  • Kinshasa School of Public Health
    Kinshasa, B.P. 11850, Congo
08

References and documents

Publications

  • Bauserman M, Lokangaka A, Gado J, Close K, Wallace D, Kodondi KK, Tshefu A, Bose C. A cluster-randomized trial determining the efficacy of caterpillar cereal as a locally available and sustainable complementary food to prevent stunting and anaemia. Public Health Nutr. 2015 Jul;18(10):1785-92. doi: 10.1017/S1368980014003334. Epub 2015 Jan 29. PubMed 25631295 ↗
09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jan 2011, a primary completion of Jun 2012 and a completion of Dec 2012. It does not say whether these dates are actual or estimated.

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

Registered
Jan 21, 2011
First posted
Jan 25, 2011
Start
Jan 2011
Primary completionActual
Jun 2012
CompletionActual
Dec 2012
Last update
Dec 9, 2013
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 Dec 9, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01282788
Collaborators
Kinshasa School of Public Health, University of California, Davis, Bill and Melinda Gates Foundation, Thrasher Research Fund
Responsible party
Carl Bose, MD (Prinicipal investigator, University of North Carolina, Chapel Hill) — Principal investigator
First posted
Jan 25, 2011
Start date
Jan 2011
Primary completion
Jun 2012
Completion
Dec 2012
Last update
Dec 9, 2013

Study contacts

Carl L Bose, MD
principal investigator · University of North Carolina, Chapel Hill

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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