Proposed Meal Changes for CACFP: Impact on Child Food Intake and Costs

Sponsor
Baylor College of Medicine (Other)
Overall Status
Completed
CT.gov ID
NCT02789215
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
32
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2
44.9
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Study Details

Study Description

Brief Summary

Child and Adult Care Food Program (CACFP) meals are an important influence on diets of children from low-income families enrolled in the CACFP and should meet children's nutrient needs while fostering healthy eating habits that enable them to maintain energy balance. Recent national data revealed that children consumed low intakes of foods that support healthy dietary patterns (whole grains, fruit and vegetables other than potatoes), but high intakes of low nutrient, energy dense foods. The 2011 USDA-commissioned Institute of Medicine (IOM) report for CACFP meals provided new recommendations that include new meal pattern requirements for the meals programs, aligning them with the U.S. Dietary Guidelines to ensure that the meals promote health and reduce inadequate and excessive intakes. The report recommended inclusion of more whole grains, fruit, vegetables, and meat/meat alternatives which will likely increase meal costs. Two of the IOM report recommendations call for research to better understand how the new meal requirements would change children's CACFP meal dietary intakes and food service costs. These are important questions, and answers are needed to inform policy and future technical and educational assistance needs. The overall objective of this project is to implement the IOM meal pattern requirements for CACFP meals in day homes and centers in Texas. The multidisciplinary team will focus on nutrition, economics, and provider outcomes. The specific aims are to assess the impact of the new meal pattern requirements on 1) Meal participation rates; 2) Provider food service costs (food, labor, total meals); and 3) Child dietary intake at CACFP homes and centers. It is hypothesized that, compared with control sites, intervention site children will select and consume healthier diets (more fruit, vegetables and whole grains) at school. A total of 32 day care sites will be recruited for the study. It is hypothesized that, compared with control sites, children at the intervention sites will select and consume healthier diets (more fruit, vegetable and whole grains) at the center. It is also hypothesized that the increase in food costs will be less than that projected in the IOM report. The results on the costs associated with creating the desired meals will be very important as these data have not been systematically collected in previous studies. This significant study targets underserved minority populations with health promoting intervention to reduce health disparities, and in addition, will inform policy on the influence of a healthy food environment on children's diet, as well as provide critical information on costs.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Proposed Meal Changes for CACFP: Impact on Child Food Intake and Costs
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
32 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Proposed Meal Changes for CACFP: Impact on Child Food Intake and Costs
Actual Study Start Date :
Sep 1, 2015
Actual Primary Completion Date :
May 1, 2017
Actual Study Completion Date :
May 31, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Receive new CACFP menu pattern

Behavioral: Proposed Meal Changes for CACFP: Impact on Child Food Intake and Costs

No Intervention: Control

Follow existing CACFP menu pattern

Outcome Measures

Primary Outcome Measures

  1. Change from Baseline Child Dietary Intake at 6 months and 12 months [Up to 12 months]

  2. Change from Baseline Meal Participation Rates at 6 months and 12 months [Up to 12 months]

  3. Change from Baseline Provider Food Service Costs (food, labor, total meals) at 6 months and 12 months [Up to 12 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
3 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Must be day care sites

  • Must be parents of children attending the day care sites

Exclusion:
  • Parents of children not attending one of the 32 day care sites

Contacts and Locations

Locations

Site City State Country Postal Code
1 Baylor College of Medicine Houston Texas United States 77030

Sponsors and Collaborators

  • Baylor College of Medicine
  • National Heart, Lung, and Blood Institute (NHLBI)

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Jayna Dave, Assistant Professor, Baylor College of Medicine
ClinicalTrials.gov Identifier:
NCT02789215
Other Study ID Numbers:
  • H-35784
  • R01HL119520
First Posted:
Jun 2, 2016
Last Update Posted:
Jan 14, 2020
Last Verified:
Jan 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Keywords provided by Jayna Dave, Assistant Professor, Baylor College of Medicine

Study Results

No Results Posted as of Jan 14, 2020