Malnutrition Clinical Trial
Official title:
Treatment of High-Risk Moderate Acute Malnutrition Using Expanded Admission Criteria (Hi-MAM Study): A Cluster-randomized Controlled Trial Protocol
This project explores whether children have better growth and cognitive development when the clinic identifies "higher risk" MAM children and support them either with the same treatment as SAM children or with the recommended practice: nutrition counseling.
This is a cluster-randomized controlled trial taking place in 20 community clinics providing
malnutrition care in Sierra Leone.
All participants will be children aged 6-59 months. Control participants will have moderate
acute malnutrition (MAM), defined as mid-upper arm circumference (MUAC) 11.5-<12.5. High Risk
MAM will be defined with a MUAC 11.5 to <11.9 or WAZ<-3.5 or Mother not the caretaker or not
breastfeeding at <2 years old. Low risk MAM defined with a MUAC 11.9 to <12.5 with no risk
factors.
Control group and low risk group caregiver's will received nutrition education via mother
care groups every two weeks for 6 weeks and will be followed up 12 and 24 weeks
post-enrollment.
High risk group will receive 1 week supply of amoxicillin at enrollment and 1 sachet of RUTF
per day till MUAC is equal to or greater than 12.5 or up to 12 weeks of treatment. Their
caregiver will also receive nutrition education via the mother care groups. The investigators
will also follow up with the participant at 12 and 24 weeks post-enrollment.
A subset of the participants in each group will also be enrolled in a cognitive development
substudy were the investigators will be using a eye tracking performance assessment.
Investigators will also enroll health adult participants for eye tracking assessment. Adult
data will be used as a reference when interpreting results.
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