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The Sanitation Hygiene Infant Nutrition Efficacy (SHINE) Trial: Protocol for school-age follow-up
Joseph D Piper1,2, Clever Mazhanga2, Marian Mwapaura2
1Blizard Institute, Queen Mary University of London, London, England, UK.
Insights
This study followed children from the SHINE trial into school age to assess the long-term effects of early interventions on health and development. Findings will inform future child health strategies.
Area of Science:
- Global Health
- Developmental Pediatrics
- Public Health Interventions
Background:
- Long-term follow-up of early-life stunting intervention trials is crucial for understanding sustained impacts.
- Holistic school-age assessments are needed to comprehensively evaluate the effects of early interventions on child development.
- The Sanitation Hygiene Infant Nutrition Efficacy (SHINE) trial provides a unique cohort for such long-term evaluations.
Purpose of the Study:
- To assess the long-term health, growth, physical, and cognitive function outcomes in children participating in the SHINE trial.
- To determine the sustained effects of improved infant and young child feeding (IYCF) and/or water, sanitation, and hygiene (WASH) interventions.
- To explore the impact of early-life exposures, maternal HIV status, and contemporary factors on school-age outcomes.
Main Methods:
- Follow-up of 1,275 children from the SHINE trial at 7-8 years of age.
- Utilized the School-Age Health, Activity, Resilience, Anthropometry and Neurocognitive (SAHARAN) toolbox for comprehensive assessments.
- Collected caregiver data on demographics, socioeconomic status, adversity, nurturing, and food/water insecurity; monthly morbidity data collected.
Main Results:
- Development of new metrics: COG-SAHARAN (cognition), GROW-SAHARAN (growth), and SUB-SAHARAN (combined function).
- Exploratory factor analysis to simplify assessment metrics.
- Annual assessments using the SUB-SAHARAN toolbox planned from ages 8-12 years.
Conclusions:
- The study establishes a framework for long-term follow-up of early-life interventions.
- The SAHARAN toolbox and derived metrics provide a comprehensive approach to school-age child assessment.
- Findings will inform public health policies and interventions for child development in low-resource settings.
Abstract:
Background: There is a need for follow-up of early-life stunting intervention trials into childhood to determine their long-term impact. A holistic school-age assessment of health, growth, physical and cognitive function will help to comprehensively characterise the sustained effects of early-life interventions. Methods: The Sanitation Hygiene Infant Nutrition Efficacy (SHINE) trial in rural Zimbabwe assessed the effects of improved infant and young child feeding (IYCF) and/or improved water, sanitation and hygiene (WASH) on stunting and anaemia at 18 months. Among children enrolled to SHINE, 1,275 have been followed up at 7-8 years of age (1,000 children who have not been exposed to HIV, 268 exposed to HIV antenatally who remain HIV negative and 7 HIV positive children). Children were assessed using the School-Age Health, Activity, Resilience, Anthropometry and Neurocognitive (SAHARAN) toolbox, to measure their growth, body composition, cognitive and physical function. In parallel, a caregiver questionnaire assessed household demographics, socioeconomic status, adversity, nurturing, caregiver support, food and water insecurity. A monthly morbidity questionnaire is currently being administered by community health workers to evaluate school-age rates of infection and healthcare-seeking. The impact of the SHINE IYCF and WASH interventions, the early-life 'exposome', maternal HIV, and contemporary exposures on each school-age outcome will be assessed. We will also undertake an exploratory factor analysis to generate new, simpler metrics for assessment of cognition (COG-SAHARAN), growth (GROW-SAHARAN) and combined growth, cognitive and physical function (SUB-SAHARAN). The SUB-SAHARAN toolbox will be used to conduct annual assessments within the SHINE cohort from ages 8-12 years. Ethics and dissemination: Approval was obtained from Medical Research Council of Zimbabwe (08/02/21) and registered with Pan-African Clinical Trials Registry (PACTR202201828512110, 24/01/22). Primary caregivers provided written informed consent and children written assent. Findings will be disseminated through community sensitisation, peer-reviewed journals and stakeholders including the Zimbabwean Ministry of Health and Child Care.
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