Improving the Eating Habits of Mother and Her Infant Via Sugar Reduction
NCT03141346 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 211
Last updated 2026-03-13
Summary
The purpose of this study is to determine whether a health education program incorporating sugar sweetened beverage and juice (SSB/J) reduction and home water delivery affects maternal and infant risk for obesity by randomizing mother-infant dyads to one of three 24-month interventions: Group 1 (control): standard health education program only; Group 2 (translation): health education program focused on sugar reduction; and Group 3 (efficacy): health education program focused on sugar reduction and bottled water delivery. The intervention program will be delivered by trained health educators during in-person home visits, or virtually via phone or video calls.
Conditions
Interventions
- BEHAVIORAL
-
Sugar reduction health education program
A health education program incorporating sugar reduction education and monitoring provided by a trained health educator over 24 months. The intervention program will be delivered by the health educator during in-person home visits, or virtually via phone or video calls.
- BEHAVIORAL
-
Control health education program
Control health education program provided by a trained health educator over 24 months. The intervention program will be delivered by the health educator during in-person home visits, or virtually via phone or video calls.
- OTHER
-
Home water delivery
Home delivery of bottled water administered over 24 months
Sponsors & Collaborators
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
collaborator NIH -
Cedars-Sinai Medical Center
collaborator OTHER - collaborator OTHER
-
University of California, San Diego
collaborator OTHER -
Children's Hospital Los Angeles
lead OTHER
Principal Investigators
-
Michael I Goran · University of Southern California; Children's Hospital Los Angeles
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 59 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-09-21
- Primary Completion
- 2023-10-21
- Completion
- 2023-10-21
Countries
- United States
Study Locations
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