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CompletedNCT05443438Updated Aug 19, 2026Results posted

Where's the Wif? Referent Selection and Retention

An interventional study of Modality - 3D-2D and Modality - 2D-3D in Healthy, sponsored by Oklahoma State University. Completed at 1 site in United States. Open to participants aged 17 Months to 30 Months, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-19.

Sponsored by Oklahoma State University · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
212
Allocation
Randomized
Ages
17 Months to 30 Months
Sex
All
01

Study summary

The goal of this work is to address increasing concerns about young children's digital media exposure and language outcomes by testing how the times course of word learning unfolds in digital environments and the cascading impact of digital media on vocabulary outcomes. The findings will have important implications for understanding when and where optimal word learning from media can occur.

Read the detailed description

The goal of the current proposal is to identify how digital media alters the mechanisms of word learning and subsequently impacts the lexical foundation on which a child's vocabulary is built. Specifically, the proposal aims to identify the impact of digital media on 1) the processes underlying real-time word learning, and 2) the processes of language generalization and vocabulary growth. Specific Aim 1 will use a novel word learning task to test children's ability to map and retain new words within and between digital media (2D images on a tablet) and real world objects (3D objects). Specific Aim 2 will probe children's novel label generalization abilities within and between 2D and 3D modalities using a novel noun generalization task. Further, individual differences in a child's prior technology experience will be measured and used to predict overall vocabulary as well as performance within and between each task. This Clinical Trial record is focused on Specific Aim 1.

02

Conditions studied

  • Healthy
03

Who can participate

Ages eligible
17 Months to 30 Months
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • between 18 and 30 months old

Exclusion criteria

Exclusion Criteria:

  • diagnosed developmental delay or disorder
  • exposure to more than 25% of another language
04

Study design

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

Study arms

  • No intervention
    3D-3D

    All items presented in 3D form

  • Experimental
    3D-2D

    Initial items in 3D, generalization in 2D

    Behavioral: Modality - 3D-2D

  • Experimental
    2D-3D

    Initial items in 2D, generalization in 3D

    Behavioral: Modality - 2D-3D

  • Experimental
    2D-2D

    Initial items in 2D, generalization in 2D

    Behavioral: Modality - 2D-2D

Interventions

  • BehavioralModality - 3D-2D

    Modality in which items will be presented (via tablet/digital media or as real object). 3D items initially and generalization as 2D

    Also known as: digital media modality

  • BehavioralModality - 2D-3D

    Modality in which items will be presented (via tablet/digital media or as real object). 2D items initially and generalization as 3D

    Also known as: digital media modality

  • BehavioralModality - 2D-2D

    Modality in which items will be presented (via tablet/digital media or as real object). 2D items initially and retention/generalization as 2D

    Also known as: digital media modality

05

What researchers measure

Primary outcomes

  1. Accuracy on Referent Selection

    Children's choices on each trial of the task will be measured. Correct responses are those to the target (prompted) item - for referent selection, this is the item asked for in the prompt (e.g. shoe, dog)

    Time frame: 1 minute

  2. Accuracy on Retention

    Children's choices on each trial of the task will be measured. Correct responses are those to the target (prompted) item - for retention, this is the item asked for in the prompt which are the correct word-object pairing for novel items previously introduced.

    Time frame: 5 minutes

06

Results

Posted Aug 19, 2026

Participant flow

Participants were recruited from Stillwater, OK and Dallas, TX

Participant flow — Overall Study
Milestone3D-3D3D-2D2D-3D2D-2D
Started55555052
Completed53514849
Not completed2423

Outcome measures

PrimaryAccuracy on Referent Selection

Children's choices on each trial of the task will be measured. Correct responses are those to the target (prompted) item - for referent selection, this is the item asked for in the prompt (e.g. shoe, dog)

Time frame:
1 minute
Reported as:
Mean · percent accuracy
Accuracy on Referent Selection
percent accuracy3D-3D3D-2D2D-3D2D-2D
Accuracy on Referent Selection77 ± 3082 ± 2685 ± 1884 ± 25
PrimaryAccuracy on Retention

Children's choices on each trial of the task will be measured. Correct responses are those to the target (prompted) item - for retention, this is the item asked for in the prompt which are the correct word-object pairing for novel items previously introduced.

Time frame:
5 minutes
Reported as:
Mean · percent accuracy
Accuracy on Retention
percent accuracy3D-3D3D-2D2D-3D2D-2D
Accuracy on Retention32 ± 2534 ± 2340 ± 2735 ± 24

Adverse events

Collected over Adverse events were not collected. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
3D-3D———
3D-2D———
2D-3D———
2D-2D———

Baseline characteristics

Age, Continuous
Age, Continuous(age in months)3D-3D3D-2D2D-3D2D-2DTotal
Mean24.4 ± 4.2923.78 ± 4.2924.2 ± 4.5724.09 ± 4.4824.12 ± 4.41
Sex: Female, Male
Sex: Female, Male(Participants)3D-3D3D-2D2D-3D2D-2DTotal
Female1619232684
Male37322523117
Race (NIH/OMB)
Race (NIH/OMB)(Participants)3D-3D3D-2D2D-3D2D-2DTotal
American Indian or Alaska Native00000
Asian30036
Native Hawaiian or Other Pacific Islander00000
Black or African American464014
White34393541149
More than one race1166326
Unknown or Not Reported10326
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)3D-3D3D-2D2D-3D2D-2DTotal
Hispanic or Latino1059731
Not Hispanic or Latino43463841168
Unknown or Not Reported00112
07

Study locations

1 site
  • Oklahoma State University
    Stillwater, Oklahoma 74078, United States
08

References and documents

Study documents

  • Protocol and statistical analysis plan · Jun 26, 2026

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — Studies proposed will be registered under the Open Science Framework (OSF) and resulting findings shared with the academic community through open science initiatives, including OSF and the sharing of videos (when permission is granted) on Databrary.

Supporting information: Study protocol, Sap, Analytic code

09

Registry details

Key details

Study ID
NCT05443438
Lead sponsor
Oklahoma State University
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Responsible party
Sarah Kucker (Assistant Professor, Oklahoma State University) — Principal investigator
First posted
Jul 5, 2022
Start date
Apr 7, 2022
Primary completion
Mar 29, 2025
Completion
Apr 30, 2025
Results posted
Aug 19, 2026
Last update
Aug 19, 2026

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 Jul 2026. You cannot join it, but the record below documents what was studied.

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