Improving the Outcomes of Community-based Management of Acute Malnutrition

Sponsor
The Hospital for Sick Children (Other)
Overall Status
Completed
CT.gov ID
NCT04582773
Collaborator
Alliance for International Medical Action (Other), University of Maiduguri Teaching Hospital (Other), Tampere University (Other)
1,087
1
15.3
71

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase

    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.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    1087 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Improving the Outcomes of Community-based Management of Acute Malnutrition
    Actual Study Start Date :
    Jul 22, 2019
    Actual Primary Completion Date :
    Oct 25, 2020
    Actual Study Completion Date :
    Oct 30, 2020

    Outcome Measures

    Primary Outcome Measures

    1. Inpatient mortality [From admission to inpatient care until the the earlier of the date of discharge from inpatient care or ten weeks after enrolment]

      survival or death during inpatient care

    Secondary Outcome Measures

    1. Number of Children receiving inpatient care who required escalation of treatment [From admission to inpatient care until the the earlier of the date of discharge from inpatient care or ten weeks after enrolment]

      transfer from unit of lower to higher level of care within inpatient treatment

    2. Number of Children receiving inpatient care who required de-escalation of treatment [From admission to inpatient care until the the earlier of the date of discharge from inpatient care or ten weeks after enrolment]

      transfer from unit of higher to lower level of care within inpatient treatment

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Month to 59 Months
    Sexes Eligible for Study:
    All
    Accepts 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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Maiduguri Teaching Hospital Maiduguri Borno Nigeria

    Sponsors and Collaborators

    • The Hospital for Sick Children
    • Alliance for International Medical Action
    • University of Maiduguri Teaching Hospital
    • Tampere University

    Investigators

    • Principal Investigator: Chris Parshuram, MD/PHD, The Hospital for Sick Children

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Christopher Parshuram, Principal Investigator, The Hospital for Sick Children
    ClinicalTrials.gov Identifier:
    NCT04582773
    Other Study ID Numbers:
    • REB1000063224
    First Posted:
    Oct 12, 2020
    Last Update Posted:
    Feb 2, 2021
    Last Verified:
    Jan 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 2, 2021