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Study identifier: NCT06599580 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Mother Screening for Relapse Using Mid-upper Arm Circumference Among Children Recovered From Severe Acute Malnutrition (Full Scale Trial)

Condition: Malnutrition, Child · Malnutrition, Infant · Malnutrition or Risk of Malnutrition  ·  Sponsor: University of California, San Francisco

PhaseNA
Planned participants2400
Who can joinAll sexes, 6 Months to 54 Months
Healthy volunteersYes

About this study

A 1:1:1 individually randomized unmasked controlled trial is proposed in which caregivers will be trained to screen their children who have recovered from an episode of SAM (severe acute malnutrition) using MUAC (mid-upper arm circumference) tapes. One arm will include caregiver screening with a mid-upper arm circumference tape and usual monthly follow-up schedule for the first 3 months post enrollment and a final follow-up at 6 months. Another arm will include caregiver screening with a mid-upper arm circumference tape and a reduced follow-up schedule for one visit at 3 months and a final visit at 6 months. The third arm will adhere to the current standard of care, which is no caregiver training to conduct mid-upper arm circumference screenings and monthly clinic-based follow-up appointments for 3 months with a final visit at 6 months post enrollment. Children aged 6-54 months with a documented recovery from uncomplicated severe acute malnutrition that was managed in a participating outpatient nutritional program and their caregivers will be eligible for inclusion in the trial. Caregivers will be trained to screen their children weekly for 6 months following discharge from the nutritional program and will be counseled to bring their child back to the nutritional program should their mid-upper arm circumference value fall in the red zone of the mid-upper arm circumference tape (\< 11.5 cm). All children will be seen at 3 and 6 months for the primary outcome assessment. By con…

This description comes directly from the study's public registry record.

Talk to the study team

Catherine Oldenburg, ScD  ·  415-502-8843  ·  catherine.oldenburg@uscf.edu

Hadley Burroughs  ·  hadley.burroughs@ucsf.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Centre de recherche en sante de nounaNouna, Burkina FasoRecruiting

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Source record: clinicaltrials.gov/study/NCT06599580