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Effectiveness Trial on Alleviation of Infant Malnutrition With Fortified Spread or Maize-Soy Flour Food Supplements

Primary Purpose

Malnutrition

Status
Completed
Phase
Phase 3
Locations
Malawi
Study Type
Interventional
Intervention
Food supplement: fortified spread
Food supplement: maize-soy flour
Sponsored by
Tampere University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malnutrition focused on measuring Infant, Malnutrition, Sub-Saharan Africa, Treatment, Growth, Haemoglobin, Fortified spread, Food supplement

Eligibility Criteria

6 Months - 15 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • signed informed consent from at least one guardian
  • age 6.00 months to 14.99 months
  • weight-for-age <-2.0 Z scores
  • availability during the period of the study
  • permanent resident Lungwena Health Centre catchment area

Exclusion Criteria:

  • moderate or severe wasting (WHM<80% of the reference median)
  • history of peanut allergy
  • history of any serious allergic reaction to any substance, requiring emergency medical care
  • history of anaphylaxis
  • severe illness warranting hospital referral
  • concurrent participation in another clinical trial with intervention to the child

Sites / Locations

  • College of Medicine, University of Malawi

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Control

LNS

CSB

Arm Description

Lipid-based nutrient supplement

Corn-soy blend supplement

Outcomes

Primary Outcome Measures

Weight gain during the 12-week follow-up (in grams)

Secondary Outcome Measures

Length gain during the 12-week follow-up (in centimetres
Change in blood haemoglobin concentration during the study period (g/l)
Change in anthropometric indices (WAZ, WHZ and HAZ)
Proportion developing moderate or severe wasting during the intervention (WHM<80% of the reference mean)
Change in mid-upper arm and head circumference

Full Information

First Posted
January 10, 2007
Last Updated
December 3, 2015
Sponsor
Tampere University
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1. Study Identification

Unique Protocol Identification Number
NCT00420758
Brief Title
Effectiveness Trial on Alleviation of Infant Malnutrition With Fortified Spread or Maize-Soy Flour Food Supplements
Official Title
LCNI-7. A Three-centre Intervention Trial in Rural Malawi, Testing the Effectiveness of Fortified Spread or Maize-Soy Flour Supplementation to Alleviate Moderate Malnutrition Among 6-18 Month Old Children
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
November 2007 (undefined)
Primary Completion Date
May 2008 (Actual)
Study Completion Date
May 2008 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study tests the hypothesis that moderately underweight but not severely wasted 6-17-month old infants receiving fortified spread or maize-spy flour as a food supplement for 12 weeks grow better during the supplementation than infants who do not get any food supplement.
Detailed Description
Childhood undernutrition is very common in rural Malawi, like in many other countries in Sub-Saharan Africa. Usually, undernutrition develops between 6 and 24 months of age. By two years of age, 30-50% of all children in rural Malawi are undernourished, predisposing them to subsequent morbidity, developmental delay and mortality. Urgent interventions are needed but the magnitude of the problem precludes a hospital-based management strategy. Therefore, emphasis must be on prevention and early home-based rehabilitation of children with mild-to-moderate malnutrition. However, the options for community based approaches are not as developed as those for institutional management of undernutrition. The present study tests a recently developed micronutrient fortified spread, FS, which offers a potential solution to home based nutrition rehabilitation. The concept has previously been shown to work not only in therapeutic feeding of undernourished children in nutrition rehabilitation units in Malawi but also home based supplementation of undernourished children aged 42 to 60 months in Mangochi District, southern Malawi. In the present study the investigators will test the efficacy in growth promotion of this product when provided as a supplementary food to moderately underweight, but not wasted, infants (defined as WAZ <-2, WHM=>80%) between 6 and 18 months of age. The study will be conducted in Lungwena area, Mangochi District, rural Malawi. A total of 291 6-15 -month old infants will be enrolled and randomised to three groups receiving different daily food supplements for 12 weeks. Children in group one (control group) will not receive any supplementation, children in group two will receive 1200 g FS 4-weekly (43 g / day) and children in group 3 will received 2000 g of fortified maize/soy flour weekly (71 g / day). Participant´s guardians will collect the food supplements from a local health centre at 4-weekly intervals. All children will undergo medical and anthropometric examinations at the beginning and end of the 12-week follow-up period. Dietary intake assessments will be conducted at 9 weeks after the onset of supplementation. A blood sample will be collected at the beginning and end of the study to measure blood haemoglobin concentration. The impact of the dietary interventions will be primarily assessed by comparing weight gain in the three intervention groups. Secondary outcomes include length gain and changes in blood haemoglobin concentration. The study will also produce descriptive data on intake of foods during the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malnutrition
Keywords
Infant, Malnutrition, Sub-Saharan Africa, Treatment, Growth, Haemoglobin, Fortified spread, Food supplement

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
299 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Title
LNS
Arm Type
Experimental
Arm Description
Lipid-based nutrient supplement
Arm Title
CSB
Arm Type
Experimental
Arm Description
Corn-soy blend supplement
Intervention Type
Dietary Supplement
Intervention Name(s)
Food supplement: fortified spread
Intervention Description
Provision of fortified spread
Intervention Type
Dietary Supplement
Intervention Name(s)
Food supplement: maize-soy flour
Intervention Description
Provision of corn-soy blend (maize-soy flour)
Primary Outcome Measure Information:
Title
Weight gain during the 12-week follow-up (in grams)
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Length gain during the 12-week follow-up (in centimetres
Time Frame
12 weeks
Title
Change in blood haemoglobin concentration during the study period (g/l)
Time Frame
12 weeks
Title
Change in anthropometric indices (WAZ, WHZ and HAZ)
Time Frame
12 weeks
Title
Proportion developing moderate or severe wasting during the intervention (WHM<80% of the reference mean)
Time Frame
12 weeks
Title
Change in mid-upper arm and head circumference
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
15 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: signed informed consent from at least one guardian age 6.00 months to 14.99 months weight-for-age <-2.0 Z scores availability during the period of the study permanent resident Lungwena Health Centre catchment area Exclusion Criteria: moderate or severe wasting (WHM<80% of the reference median) history of peanut allergy history of any serious allergic reaction to any substance, requiring emergency medical care history of anaphylaxis severe illness warranting hospital referral concurrent participation in another clinical trial with intervention to the child
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Per Ashorn, MD, PhD
Organizational Affiliation
University of Tampere, Medical School, Finland
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Kenneth Maleta, MBBS, PhD
Organizational Affiliation
University of Malawi, College of Medicine, Department of Community Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
College of Medicine, University of Malawi
City
Mangochi
State/Province
Mangochi District
Country
Malawi

12. IPD Sharing Statement

Links:
URL
http://www.medcol.mw/
Description
College of Medicine home page

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Effectiveness Trial on Alleviation of Infant Malnutrition With Fortified Spread or Maize-Soy Flour Food Supplements

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