Treating Moderate Malnutrition in 6-24 Months Old Children (LUCOMA)
Moderate Acute Malnutrition
About this trial
This is an interventional treatment trial for Moderate Acute Malnutrition focused on measuring Malnutrition, Nutritional intervention, Behavioural intervention, Burkina Faso, Cluster randomize trial
Eligibility Criteria
Inclusion Criteria:
- living in the catchment area of one of the 18 health centres participating in this cluster randomized trial
- 6-24 months of age
- -3≤ weight for height z score <-2 without edema
- No major clinical complications
- Showing appetite
Exclusion Criteria:
- Weight-for-Height Z-score <-3 and/or the presence of bilateral
- Presence of bilateral pitting oedema
- Not showing appetite
Sites / Locations
- 18 Health Centres in Houndé District
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Active Comparator
Ready-to-Use Therapeutic Foood (RUSF)
CSB++
Children Centered Counseling (CCC)
Caretakers will receive weekly RUSF, 350g, and will be advised to feed it(50 g d-1 or 3 tablespoons/day) in one meal or on demand. These are pre-defined quantities. However, minimum quantities required for a timely (≤15 days) recovery from moderate malnutrition will be determined during the pilot phase. Besides supplementary food, parents will be provided with the usual nutrition counsels prevailing currently in the health services.Children will be home-visited once a week by assessors for anthropometry, 24-hours recall of dietary and breastfeeding intake, and morbidity signs. Feeding practices will be assessed, and the changes between baseline and intervention periods evaluated. Compliance will be evaluated by interviewing family members.
Caretakers will receive weekly CSB++ (450g) rations. Parents will be advised to feed the CSB++ (65g d-1 diluted in 370 g water) in one meal or on demand. These are pre-defined quantities. However, minimum quantities of CSB++ required for a timely (≤15 days) recovery from moderate malnutrition in the area will be determined during the pilot phase. Besides supplementary foods, parents will be provided with the usual nutrition counsels prevailing currently in the health services, i.e. to keep on breastfeeding, to increase diet diversity and to feed frequent snacks. Feeding practices will be also assessed, and the changes between baseline and intervention periods evaluated. Compliance will be evaluated by interviewing family members.
The counsellor will spend 1 hour daily (during the 3 first days and then weekly) within the household for identifying enhancing and blocking factors and adapt consequently the treatment strategies in agreement with the caretakers. As in the other study arms, children will be home-visited once a week by assessors for anthropometry, 24-hours recall of dietary and breastfeeding intake, and morbidity signs. Feeding practices will be also assessed in each arm, and the changes between baseline and intervention periods evaluated. Compliance will be evaluated by interviewing family members.There will be no dietary supplements intervention, outside normal practices in Burkina.