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Improving the Nutrition Status of Infants in South-Western Uganda

Improving the Nutrition Status of 6 to 8 Months Old Children Through Diet Diversification and Better Dietary Intakes in the Kabale and Kisoro Districts in South-Western Uganda

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02098031
Acronym
CHNUDEV
Enrollment
511
Registered
2014-03-27
Start date
2014-03-31
Completion date
2016-08-31
Last updated
2024-11-20

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

Conditions

Cognitive Development, Growth, Infant Malnutrition, Nutrition Knowledge

Keywords

Child Nutrition Sciences, Growth and Development, Developing Countries

Brief summary

Undernutrition and growth restriction due to poor diet and inadequate nutrient intake continues to be a global challenge, particularly in the developing countries including Uganda. The etiology of inadequate nutrient supply to infants may relate to lack of resources or knowledge or a combination of both. Poor nutrient intake and impaired growth may affect brain and cognitive development. This study aims to evaluate nutrient intake, growth and cognitive function among children between 6 and 36 months living in the fertile Kabale and Kisoro region in south-western Uganda. The investigators hypothesize that nutrition education to mothers can bring about improved dietary intake and nutritional status among children aged 6-36 months. A follow-up study was conducted during the period January - July 2022.

Interventions

OTHERImproving nutrition knowledge among mothers

Sponsors

Kyambogo University
CollaboratorOTHER
University of Oslo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Months to No maximum
Healthy volunteers
Yes

Inclusion criteria

* A lead caretaker with a 6-8 months infant (child/lead caretaker pair) who will have given consent to participate in the study. If there is more than one child of the age in the household, the younger one will be taken as the index/study child.

Exclusion criteria

* Is older than 8 months at baseline * Congenital malformations or physical handicap that may influence growth or interfere with taking of anthropometric measurements * Disability that will influence nutrient intake * Been diagnosed with mental or brain illness as evidenced by mother or health worker. * If the family that is likely to emigrate during the study period

Design outcomes

Primary

MeasureTime frameDescription
Change in the prevalence of stunting (<-2 SD of the WHO, 2006 growth reference standards)6-8, 12-16, 20-24 (main outcome time point), 36 months, 7-10 yearsThe investigators will measure the change in stunting between the three indicated time points.

Secondary

MeasureTime frameDescription
Change in mean weight-for-age z-score6-8, 12-16 and 20-24, 36 months, 7-10 yearsThe investigators will measure the change in mean weight for age z-score between the three indicated time periods.
Change in mean weight-for-height z-score6-8, 12-16, 20-24, 36 months, 7-10 yearsThe investigators will measure the change in mean weight for height z-score between the three indicated time periods.
Change in mean Mid Upper Arm Circumference (MUAC) z-score6-8, 12-16, 20-24, 36 months, 7-10 yearsThe investigators will measure the change in MUAC between the three indicated time periods.
Change in Ages and Stages Questionnaire Scores (AQS)6-8, 12-16, 20-24, 36 monthsThe investigators will measure the change in AQS between the three indicated time periods.
Change in mean diet diversification score (DDS)6-8, 12-16, 20-24, 36 monthsThe investigators will measure the change in DDS between the three indicated time periods.
Change in The Kaufman Assessment Battery for Children (2nd ed.; KABC-II) and the Test of Variable of Attention (TOVA)7-10 yearsThe investigators will measure the change in the scores of these tests at indicated time periods.
Change in Mullens test36 monthsThe investigators will measure the change in Mullens test between the two groups after 36 months.
Change in gut microbiota20-24, 36 months, 7-10 yearsFecal samples will be collected and the investigators will measure the change in gut microbiota between the three indicated time periods.
Change in oral microbiota36 months, 7-10 yearsSaliva samples will be collected and the investigators will measure the change in oral microbiota at indicated time periods.
Change in Becks Depression Inventory II questionnaire to determine the maternal self-reported depression symptoms7-10 yearsThe investigators will measure the change in this test between the two groups at indicated time periods
Change in the Center for Epidemiological Studies Depression Scale questionnaires to determine the maternal self-reported depression symptoms7-10 yearsThe investigators will measure the change in this test between the two groups at indicated time periods
Oral health7-10 yearsThe investigators will assay caries using photographs
Change in Bayley Child Development test 3 ed.6-8, 12-16, 20-24, 36 monthsThe investigators will measure the change in Bayley Child Development test 3 ed. between the three indicated time periods.

Countries

Uganda

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026