Actively Recruiting

Phase Not Applicable
Age: 0Days +
All Genders
Healthy Volunteers
ID06072664

Fundamental Biobehavioral Mechanisms Underlying the Integrated Development of Emotion, Attachment, and Nutritive Intake in the Mother-Infant Dyad

Led by University of Michigan · Updated on 2025-10-07

150

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Michigan

Lead Sponsor

N

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

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to explore the underlying biobehavioral processes involved in how emotions, attachment, and eating behaviors develop together in mothers and their infants. The study focuses on understanding how this integrated system relates to how mothers feed their children, the children's eating habits, dietary intake, and body fat. Participants must already be enrolled in a long-term observational study to take part. The study involves 150 children from the existing observational group. Researchers will use a behavioral task called the Caloric Compensation Index (COMPX), where they offer children high- and low-calorie drinks followed by free access to a tasty snack to observe eating behavior responses. This task is done when the children are approximately 18 and 36 months old. Participants will be observed during these tasks at set ages while their food intake is measured. The main outcome is the difference in how much energy the child consumes from the snack after different calorie preload drinks. The study collects data only from children, while mothers' data is part of the larger observational study. Participation involves monitoring eating behavior and energy intake up to around 36 months of age.

CONDITIONS

Brief Title

Mother-Baby Study - Caloric Compensation Index (COMPX)

Who Can Participate

Age: 0Days +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • The child is a participant in the observational study NCT06039878.
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - Single session around ages 18 and 36 months

Participants complete a behavioral task where the child is given opportunities to consume high- and low-calorie preloads followed by free access to a palatable snack.

1 to 2 visits depending on child age

Trial Site Locations

Total: 1 location

1

University of Michigan

Ann Arbor, Michigan, United States, 48109

Actively Recruiting

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Research Team

A

Alex Jeanpierre

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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