Mother Screening for Relapse Using Mid-upper Arm Circumference Among Children Recovered From Severe Acute Malnutrition
Study Details
Study Description
Brief Summary
The investigators propose a pilot randomized controlled trial to train mothers to screen their children post-discharge for relapse based on MUAC criteria to facilitate timely identification and referral to care for children who have relapsed.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
While interventions prioritizing rapid weight gain have led to improved survival for children with severe acute malnutrition (SAM), prevention of relapse to SAM after recovery is essential to improve long-term outcomes for children beyond survival. Mothers have been successfully trained to screen for new-onset SAM in community-based settings and perform as well as community health workers for detecting SAM. Here, the investigators propose a pilot randomized controlled trial in which mothers will be trained to screen their children post-discharge for relapse based on MUAC criteria to facilitate timely identification and referral to care for children who have relapsed.
SPECIFIC AIM 1: Determine the feasibility of training mothers to screen for relapse among children recovering from SAM compared to standard of care for early detection of relapse and re-entry to care. The investigators hypothesize that relapse will be detected earlier in children whose mothers have been trained to screen for relapse compared to standard of care (no mother screening).
Specific Aim 1A: Determine the burden of post-discharge relapse among children recovered from an episode of SAM in Boromo, Burkina Faso. The investigators hypothesize that >25% of children who have recovered from SAM in the study facilities will relapse within a 6-month period following their discharge.
Specific Aim 1B: Determine the acceptability and feasibility of training mothers to screen for relapse after discharge among children recovered from SAM. the investigators hypothesize that mothers will find MUAC screening acceptable and that training them will be feasible, as demonstrated by time and costs for training, willingness to participate in training, and follow-up in the trial.
SPECIFIC AIM 2: Determine the accuracy of mother-based screening for relapse among children recovering from SAM compared to a gold standard anthropometrist. the investigators hypothesize that mother screening will have a sensitivity and specificity of > 80% for the detection of relapsed SAM (MUAC < 11.5 cm) compared to screening by a trained anthropometrist.
the investigators anticipate that the result of this pilot will provide evidence supporting the acceptability, feasibility, and accuracy of mother screening for relapse among children with SAM. The data generated during this pilot will be used to support the development of a full-scale randomized controlled trial and will be used as preliminary data supporting an R01-level NIH application. These data will help establish a new line of work for our research team in the management of acute malnutrition, which builds on existing expertise in randomized controlled trials and antibiotic-based interventions for child survival and reduction of morbidity, including as part of the management of uncomplicated SAM.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Mother screening In this arm, mothers / children dyads will be enrolled. Mothers will be trained to measure mid-upper arm circumference (MUAC) on their children weekly for 6 months. All other standard care will be provided. |
Other: Mother education on how to perform MUAC assessment
Mothers will be trained to perform MUAC weekly on their children
|
| No Intervention: standard of care In this arm, mothers / children dyads will be enrolled. No study intervention will be performed. all other standard of care will be provided. |
Outcome Measures
Primary Outcome Measures
- Time to detection of relapse [6 months]
Time to relapse using a log-rank test with a term for randomized treatment assignment will be used. Relapse will be defined using the Burkina Faso guideline for detecting malnutrition (MUAC < 11.5 cm and / or weight-for-height Z-scores WHZ < -3 SD)
Secondary Outcome Measures
- Weight for Height Z score (WHZ) [6 months]
Weight for Height Z score will be calculated and compared between arms
- weight-for-age Z-score (WAZ) [6 months]
weight-for-age Z-score will be calculated and compared between arms
- height-for-age Z-score (HAZ) [6 months]
height-for-age Z-score will be calculated and compared between arms
Eligibility Criteria
Criteria
Inclusion Criteria:
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Child is 6-59 months of age;
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Child has recovered from an episode of SAM per Burkinabè national guidelines
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Family is planning to stay in the study area for 6 months;
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Appropriate consent is obtained
Exclusion Criteria:
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Child is less than 6 months of age or more than 59 months of age
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Child didn't recover from an episode of SAM
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Family is not planning on staying in the area for 6 months
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Consent for participation is not obtained
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Centre de recherche en sante de nouna | Nouna | Burkina Faso |
Sponsors and Collaborators
- University of California, San Francisco
- Centre de Recherche en Santé de Nouna
Investigators
- Principal Investigator: Catherine Oldenburg, ScD, University of California, San Francisco
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 23-38829