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Recruiting NCT06534541

NCT06534541 Genetic Risk, Parental Feeding Practices, and Appetitive Traits in Early Life

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Clinical Trial Summary
NCT ID NCT06534541
Status Recruiting
Phase
Sponsor Trustees of Dartmouth College
Condition Childhood Obesity
Study Type INTERVENTIONAL
Enrollment 330 participants
Start Date 2024-07-18
Primary Completion 2028-08

Eligibility & Interventions

Sex All sexes
Min Age 27 Months
Max Age 72 Months
Study Type INTERVENTIONAL
Interventions
Attentional bias to food cues

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 330 participants in total. It began in 2024-07-18 with a primary completion date of 2028-08.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The preschool years (2-5 years of age) is a critical timeframe to shape the lifetime risk of obesity. While the causes of obesity are complex, appetitive traits related to overeating, such as high food approach and low food avoidance, are robustly associated with a greater BMI among children. Some children are genetically pre-disposed to expressing obesogenic appetitive traits, and those traits may mediate a genetic risk for obesity. Separately, parental feeding practices are emerging as an important, yet modifiable, influence on children's obesity risk. Coercive control feeding practices, such as strictly limiting a child's intake of highly palatable foods (restriction) and using food to control children's negative emotions (emotional feeding), are believed to be detrimental for young children because they impede self-regulatory skills around eating and may increase the saliency of highly palatable foods. The goal for this project is to disentangle the inter-relationships between coercive control feeding practices, children's obesogenic appetitive traits, and children's dietary intake across the preschool years to understand how coercive control feeding practices ultimately impact children's adiposity gain over time. Importantly, the investigators aim to understand how those effects differ based on children's underlying genetic risk for obesity. The investigators hypothesize that parents will respond to children's obesogenic appetitive traits by exhibiting more coercive control feeding practices (restriction, emotional feeding), which in turn, will promote future increase in obesogenic appetitive traits and overconsumption, leading to excess adiposity gain among children. Importantly, the investigators hypothesize children with a high genetic risk for obesity will be most susceptible to the negative effects of coercive control feeding practices because food is highly salient for them. The investigators will test the hypotheses among a cohort of children aged 2.5 years old using a longitudinal study design with repeated assessments every 6 months until children are 5 years old. If successful, study findings may be leveraged to develop tailored strategies to help parents support healthy eating behaviors among their young children that consider the heterogeneity in obesogenic appetitive traits among young children due to genetic risk factors.

Eligibility Criteria

Inclusion Criteria: * parent must be ≥18 years old, have primary custody of their child for ≥75% of the month, comprehend verbal and written English and not plan to move out of Vermont or New Hampshire during the study timeframe. * Children must be ≥2.25 and ≤2.99 years old at first visit and have normal or corrected-to-normal vision to enable eye tracking. Exclusion Criteria: * Children with any relevant food allergies or dietary restrictions, taking medication or with a medical condition that affects appetite or attention, or with a relative enrolled in the study will be excluded.

Contact & Investigator

Central Contact

Jennifer Emond, PhD

✉ jennifer.emond@dartmouth.edu

📞 1-603-646-5709

Principal Investigator

Jennifer Emond, PhD

PRINCIPAL INVESTIGATOR

Dartmouth College

Frequently Asked Questions

Who can join the NCT06534541 clinical trial?

This trial is open to participants of all sexes, aged 27 Months or older, up to 72 Months, studying Childhood Obesity. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06534541 currently recruiting?

Yes, NCT06534541 is actively recruiting participants. Contact the research team at jennifer.emond@dartmouth.edu for enrollment information.

Where is the NCT06534541 trial being conducted?

This trial is being conducted at Hanover, United States.

Who is sponsoring the NCT06534541 clinical trial?

NCT06534541 is sponsored by Trustees of Dartmouth College. The principal investigator is Jennifer Emond, PhD at Dartmouth College. The trial plans to enroll 330 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology