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NCT Number: NCT06605001

Development, Attention, and Inhibition Study

The goal of this clinical trial is to test the associations of young children's early life experiences with delaying behaviors and links with later life outcomes. The main questions it aims to answer are:

* Do experiences with waiting in early childhood predict delaying behavior in context-specific ways? * Are links between delaying behavior and life outcomes impacted by social conventions, effort and choices around delaying, or other behaviors?

Participants will:

* Complete two delaying tasks with either a sweet or wrapped gift * Complete three "Simon says"-like games that measure inhibition, cognitive flexibility and proactive control * Answer a set of questions about academic readiness * Answer a set of questions about social conventions * Complete a waiting game on the computer while a camera records eye movements * Parents will answer questions about their child's behaviors and experiences at home * Participants will return after 1 year to repeat a subset of these measures

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Key information

Age range

4 year–7 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Center for Mind and Brain

Davis, California, 95618, United States

Location status: Recruiting

Location contact

Lab Manager

CONTACT

[email protected]

530-754-4562

Yuko Munakata, Ph.D.

PRINCIPAL_INVESTIGATOR

About this study

In sessions 1 and 2, 4-6-year-olds will complete a delay of gratification task (randomly assigned to one of two groups, to delay with either a sweet or a wrapped gift), the NASA Load Index to report perceived demand and effort for the delay of gratification task, a computerized delay choice measure (while pupillometric data is collected), a Go/No-Go task, the NIH Toolbox Dimensional Change Card Sort, a Track-It task, a task measuring sensitivity to social conventions, and Woodcock-Johnson IV Tests of Achievement. Parents will complete the Child Behavioral Checklist (CBCL), the Child Behavior Questionnaire (CBQ), the REEF executive function questionnaire, and questionnaires about demographics and children's experiences waiting at mealtimes, when opening gifts, and in other contexts.

In session 3 (1 year after sessions 1 and 2), participants and parents will repeat the measures from sessions 1 and 2.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Typically developing children will be recruited. Participants will be pre-screened for developmental disorders.

Treatment and study plan

Delay of Gratification

Other

Children will complete a delay of gratification task with 1 of 2 rewards

Primary outcomes

  1. Choice Delay

    Time frame: Immediately after and 1 year after intervention

    Pattern of waiting behavior represented by area under the curve (AUC) for wait times.

  2. Executive Functions

    Time frame: Pre-intervention and 1 year after intervention

    Composite scores from the REEF, a questionnaire measuring executive functioning.

  3. Social Conventions

    Time frame: Immediately after and 1 year after intervention

    Social task measuring adherence to social conventions.

  4. Academic Readiness

    Time frame: Immediately after and 1 year after intervention

    Woodcock-Johnson IV Tests of Achievement: Letter-Word Identification and Applied Problems standardized scores.

  5. Inhibitory Control (Go/No-Go)

    Time frame: Immediately after and 1 year after intervention

    Accuracy (No-Go trials) during the Go/No-Go inhibitory control task.

  6. Experiences Waiting at Home

    Time frame: Pre-intervention and 1 year after intervention

    Composite score from a questionnaire developed for this study, measuring experiences with waiting.

  7. Cognitive Flexibility (DCCS)

    Time frame: Immediately after intervention and 1 year after intervention

    Accuracy (perseveration errors) during the Dimensional Change Card Sort (DCCS) task.

  8. Problem Behaviors

    Time frame: Pre-intervention and 1 year after intervention

    Composite and sub-scale scores from CBCL, a questionnaire measuring children's problem behaviors.

Secondary outcomes

  1. Pupil dilation during delayed choice

    Time frame: Immediately after and 1 year after intervention

    Pupil dilation while waiting for expected reward, or skipping for a new trial.

  2. Behavior while delaying

    Time frame: During initial and 1 year follow-up intervention

    Video coding of targeted behaviors (i.e., anticipatory behavior) during delay of gratification.

  3. Subjective Effort

    Time frame: During initial and 1 year follow-up intervention

    Self-reported demand and effort during the delay of gratification task on the NASA Task Load index.

  4. Proactive Control

    Time frame: During initial and 1 year follow-up intervention

    Accuracy during the Track-It proactive control task.

  5. Child Temperment

    Time frame: Pre-intervention and 1 year after intervention

    Composite score from the CBQ, a questionnaire measuring child temperament.

Study contacts

Contact information is provided by the study sponsor or research team.

Rachel Foster, B.S.

CONTACT

[email protected]

+1 530 754 4551

Yuko Munakata, PhD

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

University of California, Davis

Other

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Registry information

Official study title

Delay of Gratification: Life Habits of Delaying and Cascading Effects on Life Outcomes

Acronym: DAISY

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Sep 20, 2024
Registry last updated
Apr 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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