Integrated Treatment Protocol for Acute Malnutrition: A Non Inferiority Trial in Burkina Faso (MUAC-Only)
Primary Purpose
Global Acute Malnutrition (GAM)
Status
Completed
Phase
Not Applicable
Locations
Burkina Faso
Study Type
Interventional
Intervention
Ready to Use Therapeutic Food (RUTF)
Sponsored by
About this trial
This is an interventional treatment trial for Global Acute Malnutrition (GAM) focused on measuring MUAC, Acute malnutrition, RUTF, Children, Burkina Faso
Eligibility Criteria
Inclusion Criteria:
- Being between 6 and 59 months old
- New admission
Acute malnutrition defined as follows:
- MUAC<125mm
- MUAC> 125mm AND WHZ (Z-score) <-3 (WHO standard)
- Edema
- Resident in the study area (Yako district)
- Signed informed consent of the mother or the child's guardian
Exclusion Criteria:
- Children allergic to milk, peanuts and / or RUTF
Sites / Locations
- ALIMA
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
MUAC<125mm
Arm Description
no medical complication
Outcomes
Primary Outcome Measures
Recovery rate
The recovery is defined as below :
Minimum of 4 weeks of participation in the program
MUAC> = 125 mm on 2 consecutive visits
No edema for minimum 2 weeks
Good Clinical Health
Secondary Outcome Measures
Mortality rate
Default rate
Patient absent for 3 consecutive visits
Non-respondent rate
Patient who not reach the recovery criteria after twelve weeks in the program
Hospitalization rate
Relapse rate
Patient having reached the recovery criteria and returning for a new episode of malnutrition (MUAC<125mm).
The children's MUAC will be measured at home 3 months after program exit. For organizational and financial reasons, this data will not be collected for all children. A specific protocol explaining the sampling and organization of data collection will be annexed to the protocol.
RUTF rations
Total number of RUTF bags received per child during participation in the program.
Full Information
NCT ID
NCT03027505
First Posted
January 17, 2017
Last Updated
January 29, 2019
Sponsor
Alliance for International Medical Action
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France, Association Keoogo, Institut de Recherche en Sciences de la Sante, Burkina Faso, SOS médecins Burkina Faso
1. Study Identification
Unique Protocol Identification Number
NCT03027505
Brief Title
Integrated Treatment Protocol for Acute Malnutrition: A Non Inferiority Trial in Burkina Faso
Acronym
MUAC-Only
Official Title
Effectiveness of an Integrated Treatment Protocol for Acute Malnutrition: A Non Inferiority Trial in Passore Province (Northern Region), Burkina Faso
Study Type
Interventional
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
January 2017 (Actual)
Primary Completion Date
December 2017 (Actual)
Study Completion Date
April 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Alliance for International Medical Action
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France, Association Keoogo, Institut de Recherche en Sciences de la Sante, Burkina Faso, SOS médecins Burkina Faso
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
MUAC only is a pilot trial external control carried out between January 2017 and December 2017 in the Yako district (northern region), Burkina Faso.
The objective of this study is to evaluate an integrated protocol for acute malnourished children without medical complication. The hypotheses of the integrated protocol include :
A global treatment of acute malnutrition (moderate and severe) with a single treatment (RUTF) would improve the functioning of the program through early identification of acutely malnourished children, while achieving a better coverage and using a single supply chain.
A gradual reduction of RUTF dosage according to a child's MUAC status could significantly increase the number of children on treatment without increasing overall RUTF quantity while maintaining similar recovery rates.
Detailed Description
Objectives :
Main objective :
To ensure the recovery rate of the integrated protocol for treatment of acute malnutrition is significantly greater than 75% (reference value of the national program in BF).
Secondary objectives :
To ensure the mortality rate of the integrated protocol for treatment of acute malnutrition is significantly lower than 3% (reference value of the national BF program).
To ensure the default rate of the integrated protocol for treatment of acute malnutrition is significantly lower than 15% (reference value of the national BF program).
To ensure the non-response rate of the integrated protocol for treatment of acute malnutrition is significantly lower than 8%.
To ensure the hospitalization rate of the integrated protocol for treatment of acute malnutrition is significantly lower than 15%.
To ensure the coverage rate of the program increases by 30% after the year the integrated protocol was introduced (specific protocol annexed).
To estimate the relapse rate of the integrated protocol for treatment of acute malnutrition.
To compare RUTF rations per child of the integrated protocol compared to the national protocol
Methods :
The study population will include all acutely malnourished children aged between 6 and 59 months seeking consultations at all of the health centers in Yako District between January 2017 and December 2017.
The study will be implemented in Burkina Faso's Yako District, which includes 54 health centers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Global Acute Malnutrition (GAM)
Keywords
MUAC, Acute malnutrition, RUTF, Children, Burkina Faso
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
4958 (Actual)
8. Arms, Groups, and Interventions
Arm Title
MUAC<125mm
Arm Type
Experimental
Arm Description
no medical complication
Intervention Type
Drug
Intervention Name(s)
Ready to Use Therapeutic Food (RUTF)
Other Intervention Name(s)
MUAC<125mm
Intervention Description
MUAC used as the primary admission and exit criteria for children with MUAC <125mm and no medical complication.
Single treatment of RUTF for severe and moderate malnourished children and gradual reduction of doses according to the MUAC and the weight of the child during treatment. MUAC split into 3 categories:
MUAC <115 mm: 175 kcal /kg/day
115 <MUAC <120mm: 125kcal/kg/day
120 <MUAC <125mm: 75kcal/kg/day
Primary Outcome Measure Information:
Title
Recovery rate
Description
The recovery is defined as below :
Minimum of 4 weeks of participation in the program
MUAC> = 125 mm on 2 consecutive visits
No edema for minimum 2 weeks
Good Clinical Health
Time Frame
Between 4 and 12 weeks
Secondary Outcome Measure Information:
Title
Mortality rate
Time Frame
Between inclusion and week 12
Title
Default rate
Description
Patient absent for 3 consecutive visits
Time Frame
Between 3 and 12 weeks
Title
Non-respondent rate
Description
Patient who not reach the recovery criteria after twelve weeks in the program
Time Frame
12 weeks after inclusion
Title
Hospitalization rate
Time Frame
Between inclusion and week 12
Title
Relapse rate
Description
Patient having reached the recovery criteria and returning for a new episode of malnutrition (MUAC<125mm).
The children's MUAC will be measured at home 3 months after program exit. For organizational and financial reasons, this data will not be collected for all children. A specific protocol explaining the sampling and organization of data collection will be annexed to the protocol.
Time Frame
up to 3 months
Title
RUTF rations
Description
Total number of RUTF bags received per child during participation in the program.
Time Frame
Between inclusion and week 12
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
59 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Being between 6 and 59 months old
New admission
Acute malnutrition defined as follows:
MUAC<125mm
MUAC> 125mm AND WHZ (Z-score) <-3 (WHO standard)
Edema
Resident in the study area (Yako district)
Signed informed consent of the mother or the child's guardian
Exclusion Criteria:
Children allergic to milk, peanuts and / or RUTF
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susan Shepherd, MD
Organizational Affiliation
Directrice de recherches Opérationnelles et Médicales, ALIMA, USA
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Renaud Becquet, MPH,PhD,HDR
Organizational Affiliation
Chercheur Inserm, Inserm U1219 Bordeaux Population Health Center-Université de Bordeaux
Official's Role
Principal Investigator
Facility Information:
Facility Name
ALIMA
City
Yako
State/Province
Region Nord
Country
Burkina Faso
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Integrated Treatment Protocol for Acute Malnutrition: A Non Inferiority Trial in Burkina Faso
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