Actively Recruiting

Phase Not Applicable
Age: 6Months - 5Years
All Genders
Healthy Volunteers
ID06441305

Assessing the Impact, Implementation and Cost of Empowering Community Health Promoters to Improve Wasting Treatment Coverage in Turkana County Through Family-led MUAC Scale-up, Weight-for-age Screening, and Defaulters' Follow-up

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

1600

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

I

International Food Policy Research Institute

Lead Sponsor

U

UNICEF

Collaborating Sponsor

AI-Summary

What this Trial Is About

Child wasting is a form of severe malnutrition where a child becomes too thin, increasing the risk of illness and death. This condition requires medical consultation for treatment using medicine and nutritional supplements. However, only a small number of severely wasted children currently receive appropriate care. In Kenya, researchers are evaluating a community-based approach called SWITCH to improve detection and treatment of wasting by empowering community health promoters (CHPs) with digital tools and training. The SWITCH intervention equips CHPs with smartphones and an app to guide household visits, distribute color-coded mid-upper arm circumference (MUAC) tapes, and train caregivers to use them. CHPs send regular SMS reminders to caregivers for monitoring, measure children's weight monthly, and follow up on children who miss treatment visits through home visits. The study randomly assigns 20 of 40 community units to receive this intervention, with the other 20 continuing standard care. Participants are children aged 6 to 59 months living in the study area. Researchers will conduct baseline and follow-up surveys to measure the proportion of children receiving treatment after 24 months. They will also assess the intervention's reach, challenges, community perceptions, and costs through interviews and data collection from caregivers, CHPs, and program staff. Outcomes include treatment coverage, nutritional status measures, caregiver knowledge, and immunization rates.

CONDITIONS

Brief Title

Expanding Coverage of Severe Acute Malnutrition (SAM) Treatment in Kenya

Who Can Participate

Age: 6Months - 5Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Household is in a village covered by a community health promoter (CHP)
  • Child is between 6 months and 59.9 months of age
  • Caregiver consents to participate in the study
  • Child has one or more of the following: weight-for-height Z-score below -3, MUAC less than 115 mm, presence of bilateral edema, or is receiving treatment for severe wasting recovery
Not Eligible

You will not qualify if you...

  • Child has a congenital malformation that prevents accurate anthropometric measurements
  • Child's length is below 54 cm or height is above 120 cm

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Community-level screening based on weight and weight-for-age performed every other month.

Outpatient Treatment

Duration - Up to 24 months

Participants receive the SWITCH intervention package including digital monitoring, family-led MUAC training, and community screening every other month to improve wasting treatment coverage.

Biweekly SMS reminders to caregivers; community screening every other month aligned with Community Action Days; home visits and follow-up as needed.

Long-term Monitoring

Duration - 24 months

Participants are monitored to assess treatment coverage, program exposure, and implementation outcomes over 24 months.

Baseline and endline exhaustive screening campaigns; ongoing data collection including qualitative interviews and quantitative assessments.

Trial Site Locations

Total: 1 location

1

Turkana South and Turkana East and Aroo

Lodwar, Kenya

Actively Recruiting

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Research Team

E

Elodie Becquey, PhD

S

Sophie Ochola, PhD

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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