Actively Recruiting

Phase Not Applicable
Age: 6Months - 5Years
All Genders
Healthy Volunteers
NCT06380504

Increasing the Coverage of Severe Acute Malnutrition (SAM) Treatment in Ethiopia

Led by International Food Policy Research Institute · Updated on 2026-03-27

1080

Participants Needed

1

Research Sites

164 weeks

Total Duration

On this page

Sponsors

I

International Food Policy Research Institute

Lead Sponsor

E

Ethiopian Public Health Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

The R-SWITCH intervention aims to address the low coverage of treatment for severe wasting (SAM) by leveraging existing community groups to deliver an integrated package focused on prevention, screening, referral, and treatment of SAM. It includes behavior change communication on child nutrition and health, active screening, improved passive screening at health posts, and follow-up of referred cases and those enrolled in outpatient treatment programs (OTP). The primary objectives of the R-SWITCH studies are to assess the intervention's impact on OTP coverage, identify implementation barriers and facilitators, and evaluate its cost-efficiency and cost-effectiveness.

CONDITIONS

Official Title

Increasing the Coverage of Severe Acute Malnutrition (SAM) Treatment in Ethiopia

Who Can Participate

Age: 6Months - 5Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Child 6-59 months of age
  • Child has severe acute malnutrition (SAM) defined as MUAC less than 115mm, or bilateral pitting edema, or Weight-for-Length Z-score less than -3
  • Child is currently enrolled in a SAM outpatient treatment program (OTP)
Not Eligible

You will not qualify if you...

  • Child has anthropometric malformation or disability that prevents accurate growth measurements

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Kersa and Jeldessa woredas

Jimma, Ethiopia

Actively Recruiting

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Research Team

L

Lieven Huybregts, PhD

CONTACT

A

Alemayehu Haddis, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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