Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
NCT05781100

Investigating Baby Behavior and Family Technology Use Study

Led by California Polytechnic State University-San Luis Obispo · Updated on 2025-02-24

345

Participants Needed

1

Research Sites

232 weeks

Total Duration

On this page

Sponsors

C

California Polytechnic State University-San Luis Obispo

Lead Sponsor

U

University of Michigan

Collaborating Sponsor

AI-Summary

What this Trial Is About

Maternal sensitivity and contingent responsiveness to infant behavioral cues is an important contributor to infants' developing capacities to self-regulate. During early infancy, feeding interactions comprise a significant portion of mother-infant dyadic interactions and high-quality feeding interactions provide both nutritive and socioemotional benefits; recent data suggest that, for many dyads, mothers' sensitive responsiveness during feeding interactions is routinely impacted by the omnipresence of portable technology. The objective of the proposed research is to better understand the development and possible impacts of maternal technology use on infant feeding interactions, emotion and intake regulation, and sociobehavioral and growth outcomes.

CONDITIONS

Official Title

Investigating Baby Behavior and Family Technology Use Study

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older
  • In 3rd trimester of singleton pregnancy
  • History of healthy, low-risk pregnancy
  • Lives within 50 miles of the Cal Poly campus
  • Owns a mobile device
  • Infant was born term (gestational age 6537 weeks)
Not Eligible

You will not qualify if you...

  • Mother has an untreated medical or psychiatric condition (e.g. bipolar disorder) that could impede study participation or affect mother-infant interaction
  • Mother is participating in another interventional study that influences parenting, mother-infant interactions, feeding practices, or technology use
  • The mother is unwilling or unable to commit to longitudinal follow-ups of herself or her child
  • Infant was born preterm (gestational age 37 weeks)
  • Infant diagnosed with fetal abnormality or medical condition that interferes with oral feeding (e.g., feeding disorder, milk protein allergy) or development
  • Infant diagnosed with developmental delay (e.g., Down's syndrome)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

California Polytechnic State University

San Luis Obispo, California, United States, 93401

Actively Recruiting

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Research Team

A

Alison K Ventura, PhD

CONTACT

S

Stephanie Lechuga, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

6

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