Trial to Alleviate Malnutrition With Fortified Spread Given as a Food Supplement to Underweight Infants
Primary Purpose
Malnutrition
Status
Completed
Phase
Phase 3
Locations
Malawi
Study Type
Interventional
Intervention
Food supplement: fortified spread
Food supplement: maize and soy flour
Sponsored by
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
Inclusion Criteria: Signed informed consent from at least one guardian Ages 6.00 months to 14.99 months Weight-for-age < -2 z-scores Availability during the period of the study Permanent resident of the area Exclusion Criteria: WHZ < -3 z-scores or presence of oedema History of peanut allergy Severe illness warranting hospital referral Concurrent participation in another clinical trial with intervention to the child
Sites / Locations
- College of Medicine, University of Malawi
Outcomes
Primary Outcome Measures
Weight gain during the 12-week follow-up (in grams)
Secondary Outcome Measures
Length gain during the study period (mm)
Tibial length gain during the study period (mm)
Change in blood haemoglobin concentration during the study period (g/l)
Change in serum ferritin concentration during the study period (µg/l)
Mean change in anthropometric indices (weight-for-age z-score [WAZ], weight-for-height z-score [WHZ] and height-for-age z-score [HAZ])
Full Information
NCT ID
NCT00131222
First Posted
August 16, 2005
Last Updated
May 19, 2014
Sponsor
Tampere University
Collaborators
Academy of Finland, Foundation for Paediatric Research, Finland
1. Study Identification
Unique Protocol Identification Number
NCT00131222
Brief Title
Trial to Alleviate Malnutrition With Fortified Spread Given as a Food Supplement to Underweight Infants
Official Title
Lungwena Child Nutrition Intervention Study-4, LCNI-4. A Single-centre Intervention Trial in Rural Malawi, Testing the Potency of RUTF Supplementation to Alleviate Moderate Malnutrition Among 6-17 Month Old Infants
Study Type
Interventional
2. Study Status
Record Verification Date
April 2007
Overall Recruitment Status
Completed
Study Start Date
February 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2005 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Tampere University
Collaborators
Academy of Finland, Foundation for Paediatric Research, Finland
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study tests the hypothesis that underweight 6-17-month old infants receiving fortified spread as a food supplement for 12 weeks grow better during the supplementation than infants who are provided with maize-soy flour 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 nutrient -dense spread, ready-to use- therapeutic food (RUTF), 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 infants (defined as WAZ <-2) between 6 and 18 months of age.
The study will be conducted in Lungwena area, Mangochi District, rural Malawi. A total of 176 6-14 -month old infants will be enrolled and randomised to two groups receiving different daily food supplements for 12 weeks. Children in group one (control group) will receive 72g of fortified maize/soy flour and children in group 2 will receive 50g RUTF daily. The food supplements will be delivered to the participant's home at 3-weekly intervals.
All children will undergo medical and anthropometric examinations at 6-weekly intervals and disease symptoms monitoring every week. Dietary intake assessments will be conducted at 3 and 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 and serum ferritin concentrations. At enrolment, children's HIV status will be screened with antibody-ELISA and confirmed with HIV PCR.
The impact of the dietary interventions will be primarily assessed by comparing weight gain in the two intervention groups. Secondary outcomes include length gain, increase in tibial length and changes in blood haemoglobin and serum ferritin concentration. The study will also produce descriptive data on morbidity and 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
Single
Allocation
Randomized
Enrollment
176 (false)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
Food supplement: fortified spread
Intervention Type
Procedure
Intervention Name(s)
Food supplement: maize and soy flour
Primary Outcome Measure Information:
Title
Weight gain during the 12-week follow-up (in grams)
Secondary Outcome Measure Information:
Title
Length gain during the study period (mm)
Title
Tibial length gain during the study period (mm)
Title
Change in blood haemoglobin concentration during the study period (g/l)
Title
Change in serum ferritin concentration during the study period (µg/l)
Title
Mean change in anthropometric indices (weight-for-age z-score [WAZ], weight-for-height z-score [WHZ] and height-for-age z-score [HAZ])
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
Ages 6.00 months to 14.99 months
Weight-for-age < -2 z-scores
Availability during the period of the study
Permanent resident of the area
Exclusion Criteria:
WHZ < -3 z-scores or presence of oedema
History of peanut allergy
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
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Kenneth M Maleta, MBBS, PhD
Organizational Affiliation
Kamuzu University of Health Sciences
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
Learn more about this trial
Trial to Alleviate Malnutrition With Fortified Spread Given as a Food Supplement to Underweight Infants
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