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Improving the Outcomes of Community-based Management of Acute Malnutrition

Improving the Outcomes of Community-based Management of Acute Malnutrition

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04582773
Enrollment
1087
Registered
2020-10-12
Start date
2019-07-22
Completion date
2020-10-30
Last updated
2021-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severe Acute Malnutrition

Brief summary

Severe acute malnutrition (SAM) affects 16 million children at any one time and is responsible for the deaths of over 500,000 children under 5 years of age each year. Treatment for severe acute malnutrition is based on the Community-based Management of Acute Malnutrition (CMAM) model. The current methods used for detecting high risk children have not prevented 5% mortality observed in regions using this program. The purpose of the study is to provide evidence that objective methods for detecting high risk children can be used to optimize efficiency of Community-based Management of Acute Malnutrition (CMAM) treatment programs and thus improve child health outcomes.

Detailed description

A prospective observational study in inpatient care within community-based management of acute malnutrition(CMAM) program run by the nongovernmental organization called Alliance for International Medical Action (ALIMA) within the University of Maiduguri Teaching Hospital, Maiduguri, Nigeria The objectives of the study are to validate the BedsidePEWS scores as a measure of severity of illness in children who are treated as inpatients for severe acute malnutrition and to compare the BedsidePEWS scores with other risk factors associated for mortality and relapse of children with severe acute malnutrition. The design is a prospective observational study of 1000 children admitted as inpatients in a CMAM program in Maidaguri Teaching Hospital in Maidaguri, Nigeria. Data collection (estimated duration 4-5 months) involves vital signs, and risk factor assessment every 12 hours for duration of hospitalization. Blood test for hemoglobin and malaria will be done once upon admission. Outcomes will be measured every 12 hours and include mortality and/or escalation and de-escalation of care. Logistic regression with significance testing will be used to compare BedsidePEWS scores and risk factors between patients and among individual patients within the outcome categories. Exploratory sensitivity analyses will repeat the main logistic regression analyses to evaluate the performance of partial BedsidePEWS score in patients with missing data of 1-3 of the 7 components, by randomly removing 1-3 data elements from the score calculation from patients, and by removing systolic blood pressure from scoring.

Interventions

None listed

Sponsors

Alliance for International Medical Action
CollaboratorOTHER
University of Maiduguri Teaching Hospital
CollaboratorUNKNOWN
Tampere University
CollaboratorOTHER
The Hospital for Sick Children
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Months to 59 Months
Healthy volunteers
No

Inclusion criteria

* Aged 1 to 59 months * Diagnosed with severe acute malnutrition (criteria for severe acute malnutrition is \<3Z Weight for Height Z score, and/or MUAC \<115mm, and/or bilateral pitting oedema) * Meet the criteria for admission into inpatient care (failed appetite test, and/or medical conditions). Study amendment for inclusion: children with and without severe acute malnutrition admitted to emergency pediatric unit (EPU)

Exclusion criteria

\- Children with congenital anomalies that interfere with feeding (ie. cleft lip and/or palate); previous enrolment in this study.

Design outcomes

Primary

MeasureTime frameDescription
Inpatient mortalityFrom admission to inpatient care until the the earlier of the date of discharge from inpatient care or ten weeks after enrolmentsurvival or death during inpatient care

Secondary

MeasureTime frameDescription
Number of Children receiving inpatient care who required escalation of treatmentFrom admission to inpatient care until the the earlier of the date of discharge from inpatient care or ten weeks after enrolmenttransfer from unit of lower to higher level of care within inpatient treatment
Number of Children receiving inpatient care who required de-escalation of treatmentFrom admission to inpatient care until the the earlier of the date of discharge from inpatient care or ten weeks after enrolmenttransfer from unit of higher to lower level of care within inpatient treatment

Countries

Nigeria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026