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Effectiveness of Supplementary Feeding During Infection Among Moderately Malnourished Children (MODMAL)

Primary Purpose

Malnutrition, Infection

Status
Terminated
Phase
Not Applicable
Locations
Kenya
Study Type
Interventional
Intervention
Ready to use supplementary food (RUSF)
Sponsored by
University of Oxford
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malnutrition focused on measuring supplementary feeding, moderate malnutrition, acute infection, developing country, children

Eligibility Criteria

6 Months - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 6 months to 5 years
  • Mid-upper arm circumference (MUAC) less than 12.5 cm
  • Resident in the Kilifi demographic surveillance (DSS) area
  • Presentation with acute (<5 days) illness including respiratory infection, malaria, diarrhoeal disease or other acute infection.
  • If admitted, admission of <5 days, recruited at discharge.

Exclusion Criteria:

  • Severe malnutrition (WHZ score < -3 or Kwashiorkor)
  • Requiring admission to hospital in the opinion of clinician
  • Known allergy to maize, soya, sorghum, milk or any RUSF components.
  • Consent declined
  • Underlying condition precluding assessment or inclusion
  • Any other reason why the consenting investigator thinks it is not appropriate for them to take part.

Sites / Locations

  • Kemri Wellcome Trust Research Programme
  • Kilifi District Hospital- OPD

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Ready to use supplementary food (RUSF)

Normal diet (standard of care)

Arm Description

The RUSF intervention consists of a food paste made of maize, soya, sorghum, vegetable oil, sugar, dried skim milk and vitamin/mineral premix, prepared by VALID Nutrition in collaboration with Insta Products, Kenya in accordance with composition specified by the latest WHO expert consultation in 2008. Children in the intervention arm receive 4 weeks supply of RUSF. The amount supplied is based on the child's weight to give energy supplement of 100kcal per kg per day, equivalent to 25g RUSF per kg per day.

For equity, parents or guardians of children in the usual diet arm will be given 2 bags of maize meal(4Kg) for family consumption instead of RUSF. All parents and carers in both arms will also receive standard nutritional advice as specified in the current WHO IMCI handbook.

Outcomes

Primary Outcome Measures

Weight for Height z Score at 4 Weeks
The primary endpoint is weight for height z scores (WHZ), calculated from weight and height measures with reference to the WHO growth standards 2006. WHZ is a measure of wasting and acute malnutrition. A WHZ of zero is the median value of the reference population. Negative scores indicate undernutrition. Moderate and severe acute malnutrition are defined as WHZ<-2 and <-3 respectively. These correspond to 2 and 3 standard deviations below the reference median. Of all the anthropometric measures in regular use, WHZ and mid upper arm circumference (MUAC) have the strongest associations with infectious disease incidence and risk of death. WHZ is more appropriate than Weight for Age (WAZ), which is normally used in growth monitoring, because WAZ measures a combination of wasting and stunting (chronic malnutrition). Stunting is unlikely to be affected by short term intervention. WHZ is assessed by anthropometry, following WHO guidelines.

Secondary Outcome Measures

WHZ Score at 3 Months
MUAC for Age Z Score at 3 Months
Development of Severe Malnutrition (WHZ Score <-3 and/or Kwashiorkor)
Anemia (Hb <9.3g/dl)
Hospital Admission or Death

Full Information

First Posted
April 29, 2009
Last Updated
June 30, 2017
Sponsor
University of Oxford
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1. Study Identification

Unique Protocol Identification Number
NCT00890695
Brief Title
Effectiveness of Supplementary Feeding During Infection Among Moderately Malnourished Children
Acronym
MODMAL
Official Title
Randomized Controlled Trial of an Outpatient Strategy of Ready to Use Supplementary Food (RUSF) Among Moderately Malnourished Children With Acute Infection
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Terminated
Why Stopped
New provision of supplementary feeds for moderately malnourished children
Study Start Date
May 2009 (undefined)
Primary Completion Date
October 2009 (Actual)
Study Completion Date
November 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Oxford

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether an outpatient-based strategy of short-term, ready to use supplementary food (RUSF) among moderately malnourished children with acute infections achieves greater improvement in anthropometric measurements of wasting than usual diet.
Detailed Description
Under nutrition is a contributing factor to at least a third of child deaths. Whilst severe malnutrition has the highest mortality risk, most malnutrition-related deaths are thought to be related to mild-moderate malnutrition.This is because moderate malnutrition is common, it directly increases the risk of death from common infectious diseases and may progress to severe malnutrition. Malnutrition may arise from poverty, food insecurity or inadequate nutrition being offered, and may begin early in life. Malnutrition is exacerbated by the multiple effects of infectious diseases such as gastroenteritis, pneumonia, malaria or HIV. All these common infections are associated with net protein loss with diversion of essential amino acids to producing acute phase and immune response proteins. Fever is associated with an increased resting energy expenditure of 7 to 13% per degree Centigrade. Activation of inflammatory cascades also causes reduced appetite and loss of lean tissue and fat. Acute infection is therefore associated with growth faltering, resulting in a vicious cycle. Acute infection is therefore a potential target for intervention to interrupt the vicious cycle between malnutrition and infection in children. This study aims to evaluate a strategy of giving short-term RUSF as a supplement to usual diet at home, without daily observed feeding, administered through existing health services at Kilifi District Hospital, Kenya. RUSF has a very low moisture content and is essentially a lipid-enveloped paste, it is microbiologically stable with a long shelf life at tropical temperatures and preserves delicate micronutrients such as vitamin A.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malnutrition, Infection
Keywords
supplementary feeding, moderate malnutrition, acute infection, developing country, children

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Open label randomised trial of nutrition products
Masking
None (Open Label)
Allocation
Randomized
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ready to use supplementary food (RUSF)
Arm Type
Active Comparator
Arm Description
The RUSF intervention consists of a food paste made of maize, soya, sorghum, vegetable oil, sugar, dried skim milk and vitamin/mineral premix, prepared by VALID Nutrition in collaboration with Insta Products, Kenya in accordance with composition specified by the latest WHO expert consultation in 2008. Children in the intervention arm receive 4 weeks supply of RUSF. The amount supplied is based on the child's weight to give energy supplement of 100kcal per kg per day, equivalent to 25g RUSF per kg per day.
Arm Title
Normal diet (standard of care)
Arm Type
No Intervention
Arm Description
For equity, parents or guardians of children in the usual diet arm will be given 2 bags of maize meal(4Kg) for family consumption instead of RUSF. All parents and carers in both arms will also receive standard nutritional advice as specified in the current WHO IMCI handbook.
Intervention Type
Dietary Supplement
Intervention Name(s)
Ready to use supplementary food (RUSF)
Other Intervention Name(s)
RUSF
Intervention Description
It is a strategy of detection of moderate malnutrition and providing advice and short term provision of a standard formulation of ready to use supplementary food (RUSF) for 4 weeks with appropriate counseling on its use.The amount supplied will be based on the child's weight; 100kcal per kg per day which is equivalent to 25g RUSF per kg per day.
Primary Outcome Measure Information:
Title
Weight for Height z Score at 4 Weeks
Description
The primary endpoint is weight for height z scores (WHZ), calculated from weight and height measures with reference to the WHO growth standards 2006. WHZ is a measure of wasting and acute malnutrition. A WHZ of zero is the median value of the reference population. Negative scores indicate undernutrition. Moderate and severe acute malnutrition are defined as WHZ<-2 and <-3 respectively. These correspond to 2 and 3 standard deviations below the reference median. Of all the anthropometric measures in regular use, WHZ and mid upper arm circumference (MUAC) have the strongest associations with infectious disease incidence and risk of death. WHZ is more appropriate than Weight for Age (WAZ), which is normally used in growth monitoring, because WAZ measures a combination of wasting and stunting (chronic malnutrition). Stunting is unlikely to be affected by short term intervention. WHZ is assessed by anthropometry, following WHO guidelines.
Time Frame
between enrolment and 4 weeks
Secondary Outcome Measure Information:
Title
WHZ Score at 3 Months
Time Frame
between enrolment and 3 months
Title
MUAC for Age Z Score at 3 Months
Time Frame
between enrolment and 4 weeks and at 3 months
Title
Development of Severe Malnutrition (WHZ Score <-3 and/or Kwashiorkor)
Time Frame
at 4 weeks and 3 months
Title
Anemia (Hb <9.3g/dl)
Time Frame
at 4 weeks
Title
Hospital Admission or Death
Time Frame
from enrolment to 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 6 months to 5 years Mid-upper arm circumference (MUAC) less than 12.5 cm Resident in the Kilifi demographic surveillance (DSS) area Presentation with acute (<5 days) illness including respiratory infection, malaria, diarrhoeal disease or other acute infection. If admitted, admission of <5 days, recruited at discharge. Exclusion Criteria: Severe malnutrition (WHZ score < -3 or Kwashiorkor) Requiring admission to hospital in the opinion of clinician Known allergy to maize, soya, sorghum, milk or any RUSF components. Consent declined Underlying condition precluding assessment or inclusion Any other reason why the consenting investigator thinks it is not appropriate for them to take part.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James A Berkley
Organizational Affiliation
KEMRI-Wellcome Trust Collaborative Research Program
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kemri Wellcome Trust Research Programme
City
Kilifi
State/Province
Coast Province
ZIP/Postal Code
80108
Country
Kenya
Facility Name
Kilifi District Hospital- OPD
City
Kilifi
State/Province
Coast
ZIP/Postal Code
80108
Country
Kenya

12. IPD Sharing Statement

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Effectiveness of Supplementary Feeding During Infection Among Moderately Malnourished Children

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