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The Effect of Prior Learning on Word Learning

Identification of Treatment Parameters That Maximize Language Treatment Efficacy for Children

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05921188
Enrollment
22
Registered
2023-06-27
Start date
2023-06-01
Completion date
2025-06-06
Last updated
2025-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Language Development Disorders

Keywords

Late Talkers

Brief summary

The goal of this clinical trial is to compare two treatment conditions for late talking toddlers. In 8 weeks of word learning treatment, toddlers will be taught words that sound more like the words they already know or sound less like the words they already know. The investigators see which group learns more, to understand if choosing words that let children use the knowledge they already have helps with learning.

Detailed description

Late talking toddlers will be assigned to be in the More Familiar Sounds condition or the Less Familiar Sounds condition. Both groups will receive 8 weeks of Vocabulary Acquisition and Usage for Late Talkers (VAULT) word learning treatment (2x/week for 30 minutes per session) using their words. The investigators will compare learning within children (taught words v. control words that are not explicitly taught) to make sure the learning that is happening is due to the treatment and not just maturation. The investigators will compare across groups to see if the group treated with More Familiar Sounding words learns more than the group treated with Less Familiar Sounding words.

Interventions

BEHAVIORALVAULT Phase 4

Children will receive an input-based word learning treatment that is designed based on principles of statistical learning.

Sponsors

National Institute on Deafness and Other Communication Disorders (NIDCD)
CollaboratorNIH
University of Arizona
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Masking description

The children in the study and their caregivers will not be told which treatment group their child is in.

Intervention model description

The investigators will use treatment effect sizes to compare children to themselves (treatment v. control) and across groups (More Familiar Sounds v. Less Familiar Sounds).

Eligibility

Sex/Gender
ALL
Age
2 Years to 4 Years
Healthy volunteers
No

Inclusion criteria

* Native English Speaking * Pass pure tone hearing screening or medical report of normal hearing * 2-3 Years of age at start of study * MCDI expressive scales \<10th percentile

Exclusion criteria

* Parental reports of other diagnoses * Enrolled in concurrent treatment elsewhere * Nonverbal IQ \<75 as measured by the Bayley scales * Parents unable to consistently bring child to treatment sessions

Design outcomes

Primary

MeasureTime frameDescription
Treatment Effect SizeChange from baseline through treatment, which will average an 8-week time frame.The investigators will count the number of spontaneous and probed productions of target and control words and calculate a treatment effect size (d).
Number/Rate of Words LearnedChange from Initial Evaluation through Follow-up, which will average a 6-month time frame.The investigators will measure the number of words learned and the rate of words learned as reported by the parent on the MCDI starting prior to treatment and measured during, immediately following, and 4-6 weeks after the treatment.

Secondary

MeasureTime frameDescription
Post Treatment RetentionChange from end of treatment to follow up, which will average 4-6 weeks.The investigators will use probe data and parental report to determine how many of the words the child retained from treatment.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026