Supplementation Trial of KOKO Plus Among HIV Exposed Children in Accra
- Conditions
- HIV InfectionsNutrition PoorChild Development
- Interventions
- Dietary Supplement: KOKOPlus protein and micronutrient powder
- Registration Number
- NCT04995874
- Lead Sponsor
- Noguchi Memorial Institute for Medical Research
- Brief Summary
The overall aim of the research is to conduct a randomised controlled trial of KOKOPlus in young HIV exposed children attending HIV clinics in Accra, Ghana to test the effectiveness of KOKOPlus over a period of 6 months to improve nutritional status and child development in HIV exposed children 6-18 months of age in Accra
- Detailed Description
The specific objectives are to accomplish the following
1. To test the effectiveness of KOKOPlus to improve the nutritional status of HIV exposed infants aged 6-18 months.
2. To measure and compare nutritional status in intervention and control arms by monitoring growth in terms of height and weight over the period of 6 months
3. To measure and compare micronutrient status of intervention and control arms by comparing baseline midline and endline measurements of hemoglobin levels.
4. To measure and compare morbidity rates of intervention and control arms.
5. To measure and compare rates of achievement of child development goals between intervention and control arms using a standardized tool, the Caregiver Reported Early Development Instrument (CREDI).
6. To understand and record experiences relating to the use of KOKOPlus of mothers/caregivers in the intervention arm through focus group discussion
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 649
- Mother-infant dyads; HIV positive mothers and children between 6 and 12 months of age attending antiretroviral (ART) Clinics and child HIV Clinics.
- Mothers who decline to participate in the study
Children with severe acute malnutrition (mid-upper arm circumference <115 mm or a weight-for-height/length <-3 Z-scores of the WHO growth standards).
Children on hospital admission
Children with diagnosed or apparent congenital conditions such as encephalitis, cleft palate, hole in heart, which negatively affect the child's ability to eat and/or growth.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention KOKOPlus protein and micronutrient powder KOKOPlus protein and micronutrient powder , a complementary food supplement containing soya powder, sugar and oil along with the essential amino acid lysine and a micronutrient mix was formulated. Two weeks' supply of KOKOPlus sachets will be given to intervention arm participants every fortnight for 6 months to be mixed into any cereal, soup, stew, or other food given to the children.
- Primary Outcome Measures
Name Time Method Child developmental Milestones achieved 6 months Anthropometry 6 months Length-for-age Z score, Weight-for-age Z score. Weight for length Z score
Haemoglobin 6 months (g/dl), anaemia
- Secondary Outcome Measures
Name Time Method Morbidity 6 months Incidence of fever, malaise, loss of appetite
Trial Locations
- Locations (6)
Greater Accra Regional Hospital
🇬ðŸ‡Accra, Greater Accra, Ghana
Princess Marie Louise Children's Hospital
🇬ðŸ‡Accra, Greater Accra, Ghana
37 Military Hospital
🇬ðŸ‡Accra, Greater Accra, Ghana
Korle-bu Teaching Hospital
🇬ðŸ‡Accra, Greater Accra, Ghana
Ashaiman Polyclinic
🇬ðŸ‡Ashaiman, Greater Accra, Ghana
Tema General Hospital
🇬ðŸ‡Tema, Greater Accra, Ghana