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CompletedNCT06074926Updated Aug 27, 2024

Promoting Food Acceptance Through Positive Parenting: the Play and Grow Study

An interventional study of Associative Conditioning and Repeated Exposure in Obesity, Childhood, Overweight, Childhood and Overnutrition, sponsored by State University of New York at Buffalo. Completed at 1 site in United States. Open to participants aged 3 Years to 5 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-08-27.

Sponsored by State University of New York at Buffalo · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
3 Years to 5 Years
Sex
All
01

Study summary

Approximately one half of adults and one-fifth of children have obesity, including 14% of 2-5-year-olds. Early obesity prevention is essential as children who are overweight by age 5 are at increased risk for later obesity. Dietary intake is inextricably linked to weight status, and the majority of young children fail to meet intake recommendations, with socioeconomically disadvantaged and racial/ethnic minority children at increased risk of poor diet quality. However, children's liking of healthier foods predicts their intake, and children can learn to like healthier foods via experience. The current study brings together evidence from the parenting and learning literatures to: 1) examine effects of a novel learning strategy leveraging positive parent-child interactions on 3-5-year-old children's vegetable acceptance and dietary intake, as well as to explore 2) individual differences in learning strategy effects.

Read the detailed description

Repeated exposure, in which children taste a target food across several occasions, is an effective strategy for increasing children's acceptance and intake of healthier foods. An alternative strategy that may be preferable for those less likely to try unfamiliar or disliked foods is associative conditioning. This refers to changes in one's response to a target food after it is repeatedly, concurrently paired with an unconditioned stimulus - typically another food - that already has a positive valence. While evidence-based, this approach has the disadvantage of adding extra calories and exposure to less healthy foods.

Pilot data provided support for the hypothesis that non-food stimuli could be leveraged in conditioning strategies to promote healthier food acceptance. After pairing positive peer interactions (via group games) with tasting a target vegetable across 11 sessions, 6-8-year-old children's preferences for target vegetables increased at post-test. In considering application of this approach for younger children, positive parent-child interactions may be an appropriate non-food stimulus as parents are a primary social influence for this age group. Despite this, no studies to date have leveraged this positive stimulus in the context of associative conditioning paradigms designed to promote vegetable acceptance. Additionally, although other food preference learning approaches, like repeated exposure, are well-established in the experimental literature, less is known regarding individual differences impacting intervention effectiveness.

The current study seeks to examine effects of a novel learning strategy leveraging positive parent-child interactions on 3-5-year-old children's vegetable acceptance and dietary intake, as well as to explore individual differences in learning strategy effects. Findings will inform future intervention work, as well as offer insight into potential behavioral factors influencing young children's diet and health.

02

Conditions studied

  • Obesity, Childhood
  • Overweight, Childhood
  • Overnutrition
  • Pediatric Obesity
  • Eating, Healthy

Keywords

  • Repeated Exposure
  • Associative Conditioning
  • Positive Parenting
  • Food Acceptance
  • Diet Quality
03

In context

Pediatric Obesity

1,129 studies on the registry are indexed under Pediatric Obesity; 187 are open to participants now.

This study's enrollment of 50 is below the median of 100 across 870 interventional studies indexed under Pediatric Obesity.

Browse Pediatric Obesity studies →

Lead sponsor

State University of New York at Buffalo is the lead sponsor of 294 studies on the registry; 63 are open to participants now.

Of its 19 completed or terminated interventional studies of FDA-regulated products, 15 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years to 5 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Child is 3-5 years old
  • Parent/ guardian is 18 years of age or older
  • Child is not diagnosed with a serious physical or mental health condition that precludes safe participation
  • Parent and child are English speaking

Exclusion criteria

Exclusion Criteria:

  • The child is outside the age range of 3-5 years
  • Child is diagnosed with a serious physical or mental health condition that precludes participation
  • Parent/ guardian is less than 18 years of age
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (actual)

Study arms

  • Experimental
    Group 1 - Intervention

    Participants will attend two laboratory visits and complete a 3-week intervention, which consists of interactive parent-child activities (\~45 min of interactive activities/week) that pair tasting an assigned target vegetable with positive parent-child interactions. Positive interactions will be promoted via positive parenting prompts embedded in the activity instructions (e.g., prompts promoting child-directed play).

    Behavioral: Associative Conditioning

  • Experimental
    Group 2 - Control

    Participants will attend the same two laboratory visits and complete a 3-week intervention, which consists of only individual taste exposures to their target vegetable.

    Behavioral: Repeated Exposure

Interventions

  • BehavioralAssociative Conditioning

    There will be 3 planned activities per week (9 total) within play kits provided to families. Children will first taste their assigned target vegetable and then complete an activity with their parent following provided instructions. Activity instructions will include positive parenting skills adapted from evidence-based parenting programs (i.e., Parent-Child Interaction Therapy (PCIT) and Triple-P) designed to promote positive parent-child interactions.

  • BehavioralRepeated Exposure

    There will be 3 planned exposures per week (9 total). Exposures will include only individual tastes of the child's assigned target vegetable.

06

What researchers measure

Primary outcomes

  1. Child's target vegetable preference

    Ranked ordered preference overall (range 1-7, 7 = least preferred) and relative to control vegetable

    Time frame: Week 5 (post-test)

  2. Child's target vegetable liking

    Child-reported liking (3-point visual face scale (e.g., yummy, yucky, just OK) adapted from Birch and colleagues) overall and relative to control vegetable

    Time frame: Week 5 (post-test)

  3. Child's willingness to taste target vegetable

    Observed by study staff, defined as child placing vegetable in his/her mouth (i.e., eating the vegetable or spitting it out)

    Time frame: Week 5 (post-test)

  4. Child target vegetable ad libitum consumption

    10-minute period where child can eat as much or as little of provided foods (7 study vegetables + a neutral snack food (i.e., cracker)). Consumption will be measured via plate waste and overall consumption (grams) of the target vegetable, as well as consumption relative to the a) control vegetable and b) neutral snack will be calculated

    Time frame: Week 5 (post-test)

Secondary outcomes

  1. Reported general parenting

    Parents will complete the Comprehensive General Parenting Questionnaire (CGPQ; items rated from 1 (strongly disagree) - 5 (strongly agree), higher scores reflect higher level of parenting dimension of interest) to assess 5 dimension of general parenting (sensitivity/nurturance, structure, overprotection, coercive control, behavioral control)

    Time frame: Week 5 (post-test)

  2. Observed general parenting

    Observations of parenting will be coded from an 8-minute interactive play activity using the Iowa Family Interaction Rating Scales (IFIRS; ratings range from 1-9, 9=higher levels of behavior of interest). Aspects of parenting examined include: positive mood, warmth/support, physical affection, communication, listener responsiveness, prosocial behavior, encourages independence, intrusiveness, positive reinforcement, sensitive/child-centered, relationship quality

    Time frame: Week 5 (post-test)

  3. Observed child affect/behavior

    Observations of child affect/behavior will be coded from an 8-minute interactive play activity with a parent using the IFIRS Scales (described previously). Aspects of child affect/behavior examined include: positive mood, prosocial behavior, antisocial (i.e., externalizing) behavior

    Time frame: Week 5 (post-test)

Other outcomes

  1. Frequency of vegetables consumed by child (past week)

    Parents will report on how often their child consumed vegetables during week 4 (intervention period) via the EPOCH Preschooler Dietary Questionnaire (range: 0 to "more than once per day")

    Time frame: Week 4 (intervention period)

  2. Variety of vegetables consumed by child (past week)

    Parents will report which of 26 possible types of vegetables their child consumed during week 4 (intervention period) via the EPOCH Preschooler Dietary Questionnaire (range: 0 to 26)

    Time frame: Week 4 (intervention period)

07

Study locations

1 site
  • State University of New York at Buffalo
    Buffalo, New York 14214, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Oct 2023 to primary completion in Aug 2024, 9 months.

Of 539 non-industry interventional studies with no phase under Pediatric Obesity, half reached primary completion within 25 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 45. This study's 9 months is below that.

Counting every sponsor, half of 541 studies reached it within 25 months; a quarter within 11 and three quarters within 45.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 3, 2023
First posted
Oct 10, 2023
StartActual
Oct 30, 2023
Primary completionActual
Aug 1, 2024
CompletionActual
Aug 1, 2024
Last update
Aug 27, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 27, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06074926
Responsible party
Stephanie Anzman-Frasca (Associate Professor of Pediatrics, State University of New York at Buffalo) — Principal investigator
First posted
Oct 10, 2023
Start date
Oct 30, 2023
Primary completion
Aug 1, 2024
Completion
Aug 1, 2024
Last update
Aug 27, 2024

Study contacts

Stephanie Anzman-Frasca, PhD
principal investigator · State University of New York at Buffalo

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

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