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Reducing the Frequency of Follow up and Task Sharing in the Treatment of Uncomplicated Severe Acute Malnutrition

Primary Purpose

Severe Acute Malnutrition

Status
Completed
Phase
Not Applicable
Locations
Nigeria
Study Type
Interventional
Intervention
Standard weekly visits
Monthly visits
Sponsored by
Epicentre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Severe Acute Malnutrition

Eligibility Criteria

6 Weeks - 59 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age from 6 to 59 months
  • MUAC < 115 mm and/or grade 1-2 edema
  • Absence of current illness requiring inpatient care

Exclusion Criteria:

  • History of allergy to peanuts
  • Any other condition in which, in the judgment of the Field Investigator, would interfere with or serves as a contraindication to protocol adherence or the ability to give informed consent

Sites / Locations

  • Sokoto State Nutrition Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Standard weekly visits

Monthly visits

Arm Description

Standard weekly visits at the outpatient therapeutic feeding center until discharge

Monthly visits at the outpatient therapeutic feeding center with caregiver support for home-based surveillance, with visits scheduled at weeks 4, 8, 10 and 12 until discharge

Outcomes

Primary Outcome Measures

Nutritional recovery
Defined by being free from medical complications, MUAC > 125 mm, and no edema for 2 weeks if admitted with edema

Secondary Outcome Measures

Hospitalization
Hospitalization, defined as referral to inpatient care for weight/edema change, or failed appetite test, clinical complication necessitating inpatient care
Daily weight gain (g / kg / day) among recovered children
difference in weight (g)
Defaulting
3 missed scheduled facility visits in the weekly follow-up group and 1 missed scheduled facility visit in the monthly follow-up group
Relapse
Maternal report of admission to any therapeutic feeding program

Full Information

First Posted
April 28, 2017
Last Updated
May 11, 2020
Sponsor
Epicentre
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1. Study Identification

Unique Protocol Identification Number
NCT03140904
Brief Title
Reducing the Frequency of Follow up and Task Sharing in the Treatment of Uncomplicated Severe Acute Malnutrition
Official Title
Reducing the Frequency of Follow up and Task Sharing in the Treatment of Uncomplicated Severe Acute Malnutrition: an Evaluation of Monthly Visits and Home-based Surveillance for Access-limited and High-burden Settings
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
January 23, 2018 (Actual)
Primary Completion Date
November 30, 2019 (Actual)
Study Completion Date
April 27, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Epicentre

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will be conducted as a stratified cluster randomized trial. The unit of randomization will be the outpatient therapeutic feeding center. The 10 health centers will be stratified by size, and centers within a stratum will be randomized in a 1:1 ratio to one of two schedules of treatment: (1) standard weekly visits or (2) monthly visits with support for home-based surveillance.
Detailed Description
This study will be conducted as a stratified cluster randomized trial of a monthly schedule of follow up in the treatment of uncomplicated SAM among children aged 6 to 59 months. The unit of randomization will be the outpatient therapeutic feeding center. The 10 health centers supported by International Medical Corps UK (IMC-UK) will be stratified by size (± 1000 admissions per site per year), and centers within a stratum will be randomized in a 1:1 ratio to one of two schedules of treatment: (1) standard weekly visits or (2) monthly visits with support for home-based surveillance. Distribution of the therapeutic feeding rations, as well as medical and anthropometric surveillance, will take place on a weekly or monthly basis until discharge according to the random assignment of the site. Caregivers in the monthly visit group will receive additional instruction at admission regarding home-based MUAC measurement and clinical surveillance. Regardless of intervention assignment, all children with uncomplicated SAM will receive standard medical care on admission as per national guidelines, and a home visit 2 months following discharge from the nutritional program. Additional data collection, including coverage assessment and economic costing analysis will be used to address the secondary objectives related to the evaluation of coverage and cost-effectiveness, respectively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Acute Malnutrition

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Standard weekly visits at the outpatient therapeutic feeding center until discharge Monthly visits at the outpatient therapeutic feeding center with caregiver support for home-based surveillance, with visits scheduled at weeks 4, 8, 10 and 12 until discharge.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
3945 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard weekly visits
Arm Type
Other
Arm Description
Standard weekly visits at the outpatient therapeutic feeding center until discharge
Arm Title
Monthly visits
Arm Type
Other
Arm Description
Monthly visits at the outpatient therapeutic feeding center with caregiver support for home-based surveillance, with visits scheduled at weeks 4, 8, 10 and 12 until discharge
Intervention Type
Other
Intervention Name(s)
Standard weekly visits
Intervention Description
Distribution of the therapeutic feeding rations, as well as medical and anthropometric surveillance, will take place on a weekly basis at the outpatient therapeutic feeding center according to the random assignment of the site, until discharge
Intervention Type
Other
Intervention Name(s)
Monthly visits
Intervention Description
Distribution of the therapeutic feeding rations, as well as medical and anthropometric surveillance, will take place on a monthly basis at the outpatient therapeutic feeding center according to the random assignment of the site, until discharge
Primary Outcome Measure Information:
Title
Nutritional recovery
Description
Defined by being free from medical complications, MUAC > 125 mm, and no edema for 2 weeks if admitted with edema
Time Frame
Minimum length of stay is 8 weeks
Secondary Outcome Measure Information:
Title
Hospitalization
Description
Hospitalization, defined as referral to inpatient care for weight/edema change, or failed appetite test, clinical complication necessitating inpatient care
Time Frame
within 2 months
Title
Daily weight gain (g / kg / day) among recovered children
Description
difference in weight (g)
Time Frame
within 2 months
Title
Defaulting
Description
3 missed scheduled facility visits in the weekly follow-up group and 1 missed scheduled facility visit in the monthly follow-up group
Time Frame
within 2 months
Title
Relapse
Description
Maternal report of admission to any therapeutic feeding program
Time Frame
Within 2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Weeks
Maximum Age & Unit of Time
59 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age from 6 to 59 months MUAC < 115 mm and/or grade 1-2 edema Absence of current illness requiring inpatient care Exclusion Criteria: History of allergy to peanuts Any other condition in which, in the judgment of the Field Investigator, would interfere with or serves as a contraindication to protocol adherence or the ability to give informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rebecca GRAIS
Organizational Affiliation
Epicentre
Official's Role
Study Director
Facility Information:
Facility Name
Sokoto State Nutrition Centre
City
Sokoto
Country
Nigeria

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Subject to individual data sharing agreements
Citations:
PubMed Identifier
35231024
Citation
Hitchings MDT, Berthe F, Aruna P, Shehu I, Hamza MA, Nanama S, Steve-Edemba C, Grais RF, Isanaka S. Effectiveness of a monthly schedule of follow-up for the treatment of uncomplicated severe acute malnutrition in Sokoto, Nigeria: A cluster randomized crossover trial. PLoS Med. 2022 Mar 1;19(3):e1003923. doi: 10.1371/journal.pmed.1003923. eCollection 2022 Mar.
Results Reference
derived
PubMed Identifier
31842870
Citation
Isanaka S, Hedt-Gauthier BL, Salou H, Berthe F, Grais RF, Allen BGS. Active and adaptive case finding to estimate therapeutic program coverage for severe acute malnutrition: a capture-recapture study. BMC Health Serv Res. 2019 Dec 16;19(1):967. doi: 10.1186/s12913-019-4791-9.
Results Reference
derived

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Reducing the Frequency of Follow up and Task Sharing in the Treatment of Uncomplicated Severe Acute Malnutrition

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