Feeding Young Children Study: Bottle Weaning Intervention
NCT ID: NCT00756626
Last Updated: 2018-06-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
300 participants
INTERVENTIONAL
2008-10-31
2011-12-31
Brief Summary
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COMPONENTS OF THE 'FEEDING YOUNG CHILDREN STUDY' (FYCS):
1. Randomized Controlled Trial (RCT)- of a bottle-weaning intervention in low-income multi-ethnic toddlers, will enroll n=464 12 month olds using \>2 bottles/day from two WIC sites. Bottle use, anthropometrics, dietary intake, and nutrient density outcomes will be assessed at Baseline, and 4 times over a 12 month follow-up.
2. Observational Study- nested within the RCT, will describe dietary intake and nutrient density data (24 hour recalls) for this period of feeding transitions. FYCS fills a gap in knowledge about this population's dietary habits, and their relationship to bottle use.
3. Extension- our Marketing Department will produce: a 5-8 minute 'infomercial' and nutritionist and client guides (freely downloadable) at WIC, maternal/child health, and pediatric websites, and; a public TV segment. We will disseminate findings through a) the National WIC Association, b) nutrition \& pediatric journals, and; c) lay print, media, and websites with assistance from our Public Relations Department.
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Detailed Description
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The Feeding Young Children Study (FYCS) is a randomized controlled trial (RCT) of a bottle-weaning intervention aimed at reducing the risk of overweight in low-income multi-ethnic toddlers in WIC.
Aim #1: To reduce inappropriate bottle-feeding practices (RCT)
1.The Intervention group will reduce inappropriate feeding practices, as measured by: absolute weaning; # of bottles; ounces consumed from bottles; and content, pattern \& timing of bottles.
Aim#2: To decrease the risk of overweight in children (RCT)
1. The Intervention group will see a decrease in the percentage of children \>85th percentile weight-for-length, and \> 95th % ile weight-for-length over the 12 month follow-up.
2. The Intervention group will have lower age- and sex-adjusted weight-for-length z scores; and a decreased weight gain velocity over the 12 month follow-up, compared with Controls.
Aim #3: To understand dietary intake \& nutrient density (Observational Study)
1\. We will describe beverage and food intakes and nutrient density at baseline and over time in relation to bottle use patterns and anthropometrics, for the sample and by treatment group.
Aim #4: To produce sustainable products and widely disseminate findings (Extension)
1. We will produce a 5-8 minute bottle-weaning infomercial, and nutritionist and client guides for download from WIC,15 maternal/child health16,17 and pediatric18 websites-- as well as a segment for "Keeping Kids Healthy," a nationally syndicated, Emmy award winning TV show.
2. We will extend findings through a) lay print, media, and web outlets via Public Relations; b) the National WIC association; and c) nutrition \& pediatric journal papers.
We will enroll n=464 12 month olds who are drinking \>2 (non-water) bottles or sippy cups/day, from 2 Bronx WIC sites. Bottle/sippy cup use, anthropometrics, and dietary intake will be assessed at Baseline, and again at 15, 18, 21, and 24 months of age. FYCS nutritionists (blinded to group assignment) will collect two 24 h recalls of all beverage and solid intake, and enter it into the Windows-based Nutrition Data Systems for Research software, the premiere dietary data collection and nutrient density calculation tool. WIC nutritionists will administer the Intervention at Baseline, and (blinded to outcomes) as needed at follow-ups.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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1
Intervention group receives bottle weaning intervention from WIC nutritionist
Bottle Weaning Intervention
WIC Nutritionist will deliver bottle weaning intervention education with participants in intervention group at 12 month baseline and at 15, 18, 21, and 24 month follow-up as needed
2
Control standard of care
No interventions assigned to this group
Interventions
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Bottle Weaning Intervention
WIC Nutritionist will deliver bottle weaning intervention education with participants in intervention group at 12 month baseline and at 15, 18, 21, and 24 month follow-up as needed
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* On chronic medications that may affect the child's appetite or growth rate.
* Medical conditions that may affect the child's appetite or growth rate.
* Neurological or muscular conditions that affect the child's ability to feed themselves.
* Steroid treatments such as prednisone that may affect the growth rate of the child.
12 Months
13 Months
ALL
No
Sponsors
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United States Department of Agriculture (USDA)
FED
Montefiore Medical Center
OTHER
Responsible Party
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Karen Bonuck
Principal Investigator
Principal Investigators
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Karen A. Bonuck, PhD
Role: PRINCIPAL_INVESTIGATOR
Albert Einstein College of Medicine
Locations
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Westchester Square WIC
The Bronx, New York, United States
Countries
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References
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Bonuck K, Avraham SB, Lo Y, Kahn R, Hyden C. Bottle-weaning intervention and toddler overweight. J Pediatr. 2014 Feb;164(2):306-12.e1-2. doi: 10.1016/j.jpeds.2013.09.029. Epub 2013 Oct 31.
Other Identifiers
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USDA 2007-004556
Identifier Type: -
Identifier Source: secondary_id
03-11-295E
Identifier Type: -
Identifier Source: org_study_id
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