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Mothers Understand And Can do it - Mid Upper Arm Circumference Screening for Malnutrition Performed by Mothers (MUAC)

A

Alliance for International Medical Action

Status

Completed

Conditions

Malnutrition
Malnutrition; Degree, Moderate
Kwashiorkor
Marasmus

Study type

Observational

Funder types

Other

Identifiers

NCT01790815
MUAC mères

Details and patient eligibility

About

PRIMARY OBJECTIVE :

To determine whether mothers, given minimal group training, are capable of using a MUAC (mid-upper arm circumference) bracelet to screen their children for malnutrition and categorise them into one of three groups : 'red' (SAM ; severe acute malnutrition), 'yellow' (MAM ; moderate acute malnutrition) or 'green' (normal nutritional status)

SECONDARY OBJECTIVES :

To establish whether there is a difference in the MUAC value if measured on the right arm as opposed to the left, in young children

To determine whether there is a difference in the MUAC value if the mid upper arm position is determined visually as opposed to being measured in the 'classical' fashion

Full description

Severe Acute Malnutrition (SAM) and its complications are major causes of death in under 5s in the developing world. A simple, reproducible, scalable way to recognise acute malnutrition and target early intervention would be a huge advance. Can mothers with limited training reliably measure and interpret the results of Mid Upper Arm Circumference (MUAC), a measurement performed with a MUAC measuring tape costing $0.06? MUAC contrasts with Z-score (WHZ), which requires both scales and a height gauge, both health worker interventions susceptible to considerable error, sensitive to non-nutritional factors, requiring calculations and growth curves, yet much less accurate in predicting risk of death compared with MUAC.

Enrollment

300 patients

Sex

All

Ages

6 to 59 months old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • children present in the inpatient malnutrition treatment unit and paediatric service of the Mirriah district hospital aged between 6-59 months old
  • children aged between 6-59 months old in the two villages where the community phase of the study was conducted

Exclusion criteria

  • children receiving treatment in the intensive care unit of Mirriah district hospital
  • children with bilateral oedema
  • children whose mothers or fathers refused consent to participate in the study

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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