Comparison of an Alternative Therapeutic Food for the International Food Aid Market to a Standard Ready-to-use Therapeutic Food (RUTF) for the Treatment of Severe Acute Malnutrition in Children

Not Applicable

Completed

• Conditions: Malnutrition
• Interventions: Dietary Supplement: Alternative RUTF; Dietary Supplement: Standard RUTF

• Registration Number: NCT03407326
• Lead Sponsor: Washington University School of Medicine

Brief Summary

In this clinical non-inferiority trial, two foods will be compared for the treatment of SAM, testing the hypothesis that the difference in recovery rates and growth between the two test groups will be no greater than 5 percent.

Detailed Description

This will be a randomised, triple-blinded, controlled clinical non-inferiority trial assessing the treatment of SAM with one of two therapeutic foods until the child is recovered or for a period of up to 12 weeks.

Subjects will be recruited from rural health clinics in the Western Rural Region and Pujehun District of Sierra Leone, due to the limited accessibility of treatment programs in this area; investigators believe a clinical trial in this district will be beneficial.

Sierra Leonean children aged 6-59 months with uncomplicated SAM (with WHZ \< -3, MUAC of \<11.5 cm, or bipedal edema) will be recruited at health clinics in the Western Rural Region and Pujehun District. A total of 1,300 children will be enrolled for a total sample size of 1,262 (631 per treatment) from 30 PHU centers, to detect a 5% difference in recovery rates between any two foods, with 95% sensitivity and 80% power, assuming that the standard recovery rate is 85% and a binary non-inferiority test.

After screening and enrolment, each child's participation will last up to 12 weeks. If a child recovers before the end of the 12-week period, a child's WHZ reaches and stays above -2 for two consecutive visits without edema, the child will graduate from the study. No study food products will be given to children after 12 weeks of participation; those who have not recovered will be taken for inpatient treatment. Children will enter the study on a rolling enrolment basis and will continue to be enrolled until 1,300 children complete the study.

Random allocation of food intervention will be conducted by nurses who will have the caregiver draw opaque envelopes containing one of 4 colours. Caretakers chose a sealed envelope that contains 1 of 4 colours: 2 of these colours correspond to the control food and 2 to the experimental food. The colour will be recorded separately from the child's clinical measurements and researchers involved in the randomization process do not know which colour corresponds to which food corresponding to one of the therapeutic foods. The code will be accessible only to the food distribution personnel, who do not assess participant outcomes or eligibility. Investigators performing clinical assessments and caretakers will be blinded to the child's assigned food group.

A sub-set of participants in the main study will undergo eye-tracking testing to evaluate neurocognitive function and recovery in children with severe acute malnutrition after receiving therapeutic food.

Study Timeline

• Study First Submitted: 2018-01-16
• Study First Submitted QC: 2018-01-16
• Study First Posted: 2018-01-23
• Study Start: 2018-10-16
• Primary Completion: 2019-09-02
• Study Completion: 2019-09-02
• Status Verified: 2020-01
• Last Update Submitted: 2020-01-08
• Last Update Posted: 2020-01-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 1568

Inclusion Criteria

Children aged 6-59 months with one or combination of the following

• WHZ < -3
• MUAC <11.5cm
• bipedal edema

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Exclusion Criteria

• children currently involved in another research trial or feeding program
• developmentally delayed
• chronic debilitating illness (such as cerebral palsy)
• history of peanut or milk allergy

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Alternative	Alternative RUTF	Participants will receive approximately 190 kcal/kg/day of alternative RUTF till recovery or up to 12 weeks of treatment.
Standard	Standard RUTF	Participants will receive approximately 190 kcal/kg/day of standard RUTF till recovery or up to 12 weeks of treatment.

Primary Outcome Measures

Name	Time	Method
Mid-upper-arm circumference	2 to 12 weeks	MUAC ≥ 12.5
Weight-for-height z score	2 to 12 weeks	WHZ≥-2

Secondary Outcome Measures

Name	Time	Method
Adverse symptoms	2 to 12 weeks	stomach pain, vomiting, diarrhoea, rash or fever

Trial Locations

Locations (1)

Project Peanut Butter; 🇸🇱 Freetown, Sierra Leone