Acceptability of LNS for Infants and Young Children in Guatemala
NCT01148641 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 43
Last updated 2018-01-29
Summary
This study aims to assess the acceptability of lipid-based nutrient supplements (LNS) for use as nutritional supplements for infants and young children in Guatemala.
The study was conducted in three phases. Phase 1 was a test-feeding to compare the acceptability of two different flavors of LNS (peanut and cinnamon) in infants and young children and their mothers or caregivers in terms of taste, smell and texture, as well as amount of the test-dose consumed. In Phase 2, children in the Phase 1 trial received a 2-week supply of one of the LNS products, which they consumed daily in their homes for 14 days under real-life conditions. Direct observation of supplement use and in-depth interviews with mothers, caregivers and health staff providing services in communities will be part of this phase too. In Phase 3, focus group discussions (FGD) were held with participants (mothers and caregivers) as well as with health staff providing services in communities to discuss different aspects of infant and child feeding and best ways for the LNS product to be used in the context of Guatemala.
We hypothesized that both flavors of LNS would be accepted by Guatemalan infants and young children children and their mothers or caregivers.
Conditions
- Malnutrition
Interventions
- DIETARY_SUPPLEMENT
-
LNS
Infants and young children will receive 10 g of LNS for test trial during 3 consecutive days (crossover design) and thereafter, 20 g per day for 14 days.
Sponsors & Collaborators
-
FHI 360
collaborator OTHER -
University of California, Davis
lead OTHER
Principal Investigators
-
Kathryn G Dewey, PhD · University of California, Davis
Eligibility
- Min Age
- 6 Months
- Max Age
- 18 Months
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2010-05-31
- Primary Completion
- 2010-07-31
- Completion
- 2010-11-30
Countries
- Guatemala
Study Locations
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