Development, Attention, and Inhibition Study (DAISY)

April 10, 2026 updated by: University of California, Davis

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

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

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

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.

Study Type

Interventional

Enrollment (Estimated)

200

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • California
      • Davis, California, United States, 95618
        • Recruiting
        • Center for Mind and Brain
        • Contact:
        • Principal Investigator:
          • Yuko Munakata, Ph.D.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

Yes

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Delay of Gratification - Treat
Reward presented is a sweet treat.
Children will complete a delay of gratification task with 1 of 2 rewards
Experimental: Delay of Gratification - Gift
Reward presented is a wrapped gift.
Children will complete a delay of gratification task with 1 of 2 rewards

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
Immediately after and 1 year after intervention
Executive Functions
Time Frame: Pre-intervention and 1 year after intervention
Composite scores from the REEF, a questionnaire measuring executive functioning.
Pre-intervention and 1 year after intervention
Social Conventions
Time Frame: Immediately after and 1 year after intervention
Social task measuring adherence to social conventions.
Immediately after and 1 year after intervention
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.
Immediately after and 1 year after intervention
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.
Immediately after and 1 year after intervention
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.
Pre-intervention and 1 year after intervention
Cognitive Flexibility (DCCS)
Time Frame: Immediately after intervention and 1 year after intervention
Accuracy (perseveration errors) during the Dimensional Change Card Sort (DCCS) task.
Immediately after intervention and 1 year after intervention
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.
Pre-intervention and 1 year after intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
Immediately after and 1 year after intervention
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.
During initial and 1 year follow-up intervention
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.
During initial and 1 year follow-up intervention
Proactive Control
Time Frame: During initial and 1 year follow-up intervention
Accuracy during the Track-It proactive control task.
During initial and 1 year follow-up intervention
Child Temperment
Time Frame: Pre-intervention and 1 year after intervention
Composite score from the CBQ, a questionnaire measuring child temperament.
Pre-intervention and 1 year after intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Rachel Foster, B.S., University of California, Davis

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 21, 2024

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

September 10, 2024

First Submitted That Met QC Criteria

September 17, 2024

First Posted (Actual)

September 20, 2024

Study Record Updates

Last Update Posted (Actual)

April 15, 2026

Last Update Submitted That Met QC Criteria

April 10, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 1518244
  • R01HD086184 (U.S. NIH Grant/Contract)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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