NCT06981429

Brief Summary

This study is the pilot of a 12 - week positive food parenting intervention focused on structure-based and autonomy promoting practices. The intervention aims to give parents the tools to promote healthy child growth and improve diet quality. The investigators are piloting to assess feasibility and efficacy of the intervention through examining participant retention, impact on parent feeding practices, and impact on parent and child diet quality.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started May 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 6, 2025

Completed
13 days until next milestone

Study Start

First participant enrolled

May 19, 2025

Completed
1 day until next milestone

First Posted

Study publicly available on registry

May 20, 2025

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 26, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 26, 2026

Completed
Last Updated

May 29, 2025

Status Verified

May 1, 2025

Enrollment Period

9 months

First QC Date

May 6, 2025

Last Update Submit

May 28, 2025

Conditions

Keywords

childrenparentingparent feeding practicesfood parentingobesity riskpositive food parentingautonomy promotionstructure - based food parenting

Outcome Measures

Primary Outcomes (3)

  • Parent use of structure - based and autonomy - promoting parent feeding practices.

    Compare responses to validated questionnaires measuring food parenting practices from session 1 to session 12.

    Session 1 (week 1) to Session 12 (week 12)

  • Parent and Child Diet Quality

    Compare change in parent and child healthy eating index (HEI) from session 1 to session 12. The healthy eating index (HEI) is a measure of how a participants diet aligns with the recommendations by the Dietary Guidelines for Americans (Dietary Guidelines). Possible scores range from 0 (does not align at all with recommendations by the Dietary Guidelines for Americans) to 100 (perfectly aligns with recommendations by the Dietary Guidelines for Americans). Higher scores mean a better outcome.

    Session 1 (week 1) and Session 12 (week 12)

  • Parent BMI and Child zBMI

    Change in parent BMI and child zBMI from session 1 to session 12.

    Session 1 (week 1) and Session 12 (week 12)

Study Arms (2)

Experimental Group - Positive Food Parenting Intervention

EXPERIMENTAL

Participants randomly assigned to the experimental group.

Behavioral: Nourish to Flourish: The Power of Positive Food Parenting

Control Group

NO INTERVENTION

Participants randomly assigned to the control group.

Interventions

This intervention focuses on increasing diet quality and parent use of positive food parenting practices with the goal of promoting healthy child growth). This will be a 12 - week, 12 session study. Sessions 1 and 12 will consist of collection baseline and post-intervention data. Sessions 2 - 11 will be a mix of online - group sessions and individual online or in - person sessions (based on participant preference). The group sessions are focused on principal investigator presentation of the intervention curriculum and group discussion. The individual sessions are focused on goal setting, coping planning, and working through individual situations with a trained coach.

Experimental Group - Positive Food Parenting Intervention

Eligibility Criteria

Age5 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Age \> 18 years old.
  • Have a child between the ages of 5 - 11 who is at risk for obesity (child BMI percentile \> 85th) or parent it concerned about their child developing overweight or obesity
  • Low use of positive food parenting (Defined as: low reports of individual nutrition education/ knowledge OR reports low levels of structure, involvement, or encouragement in their food parenting practices)
  • Must be responsible for feeding their eligible child at least 50% of the time.
  • Fluent in English.
  • Have access to internet and a Zoom compatible device.

You may not qualify if:

  • Age is \< 18 years old. Their child is determined ineligible (based on BMI percentile and age).
  • Does not report low use of positive food parenting (as defined above).
  • Is responsible for feeding their eligible child \< 50% of the time.
  • Not fluent in English.
  • Does not have access to internet and a Zoom compatible device.
  • On medication that could influence their eating or feeding behaviors.
  • CHILD CRITERIA:
  • Their parent/ guardian is eligible and participating in the study.
  • Ages 5 - 11
  • Is not current diagnosed with a clinical eating disorder (ED).
  • Is not on any medications, or have any conditions, that could influence the child's taste, appetite, or olfactory sensory responsiveness.
  • Their parent/ guardian is not eligible nor participating in the study.
  • Below the age of 5 and above the age of 11.
  • BMI percentile \< 85th and/or \> 97th.
  • Current diagnosis of a clinical eating disorder (ED)
  • +1 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

State University of New York at Buffalo, South Campus

Buffalo, New York, 14214, United States

RECRUITING

MeSH Terms

Conditions

Pediatric ObesityNutrition Disorders

Condition Hierarchy (Ancestors)

ObesityOverweightOvernutritionNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Katherine N Balantekin, PhD, RD

    Assistant Professor, University at Buffalo

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Katherine N Balantekin, PhD, RD

CONTACT

Hannah E Kolpack, BS

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Participants will either be assigned to the control group or the experimental group. The control group will participate in a 10 - session 'promoting healthy development in middle childhood' program. The experimental group will be receiving the intervention.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

May 6, 2025

First Posted

May 20, 2025

Study Start

May 19, 2025

Primary Completion

February 26, 2026

Study Completion

February 26, 2026

Last Updated

May 29, 2025

Record last verified: 2025-05

Locations