Mealtime Interactions and Risk of Toddler Obesity

NCT ID: NCT02766218

Last Updated: 2021-02-04

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

173 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-09-30

Study Completion Date

2019-06-30

Brief Summary

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The purpose of this observational study is to conduct 18-, 24-, and 36-month assessments with mother-toddler dyads who participated in a study that is testing the effects of a multicomponent lifestyle intervention as a means to prevent excessive gestational weight gain in obese women. Specifically, dyads will be invited to participate in home-based assessments to videotape an evening meal, have anthropometric measures taken, and complete study questionnaires. The overall goal is to understand factors related prospectively to responsive feeding between mothers and toddlers at 18 months; determine whether responsive feeding at 18 and 24 months predicts change in zBMI and adiposity from 18-36 months; and explore which factors are most strongly predictive of child zBMI change from birth to 36 months.

Detailed Description

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Conditions

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Obesity

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Behavioral: Lifestyle Intervention

The intervention is a multicomponent program designed to prevent excessive gestational weight gain in obese women through modifications of diet, exercise, and behavioral strategies during pregnancy.

No interventions assigned to this group

No Intervention: Standard Care

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Mother participated in clinical trial #NCT01545934
* Child 18-36 months old

Exclusion Criteria

* Child chronic health conditions that could affect feeding or growth (diagnosed feeding disorders, use of feeding tube) or could influence the mealtime interaction (significant food allergies or dietary restrictions, diagnosed psychiatric disorders, or pervasive developmental delays).
Minimum Eligible Age

18 Months

Maximum Eligible Age

36 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Miriam Hospital

OTHER

Sponsor Role collaborator

California Polytechnic State University-San Luis Obispo

OTHER

Sponsor Role collaborator

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

NIH

Sponsor Role collaborator

Temple University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Chantelle Hart, PhD

Role: PRINCIPAL_INVESTIGATOR

Temple University

Suzanne Phelan, PhD

Role: PRINCIPAL_INVESTIGATOR

California Polytechnic State University-San Luis Obispo

Rena Wing, PhD

Role: PRINCIPAL_INVESTIGATOR

The Miriam Hospital

Other Identifiers

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R01DK108661

Identifier Type: NIH

Identifier Source: secondary_id

View Link

R56DK108661

Identifier Type: NIH

Identifier Source: secondary_id

View Link

23356

Identifier Type: -

Identifier Source: org_study_id

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