Actively Recruiting

Phase Not Applicable
Age: 18Months - 30Months
All Genders
Healthy Volunteers
ID06156865

Neuroimaging Reveals Treatment-related Changes in Developmental Language Disorder: A Randomized Controlled Trial Supplement

Led by University of Toronto · Updated on 2026-06-02

45

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Toronto

Lead Sponsor

H

Holland Bloorview Kids Rehabilitation Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Late talking affects about 10% to 20% of children under 3 years old and is marked by delays in vocabulary and grammar similar to those seen in preschoolers with developmental language disorder (DLD). Researchers are studying the brain and behavioral factors that influence late talking, aiming to better understand the memory and language processes involved and how they relate to changes from treatment. This study builds on existing research about memory systems and brain structures involved in language learning. The study compares children with late talking who receive a structured intervention program to improve grammar, vocabulary, and communication, with those who do not receive treatment during the study. The intervention includes teaching parents and providing direct support to children over 6 to 8 weeks. Additionally, typically developing peers are included to help understand differences related to late talking. Brain imaging using diffusion techniques will measure changes in brain connectivity before, after, and following a break in treatment. Participants will undergo brain scans and behavioral assessments at multiple points: before the intervention, after 6 to 8 weeks of treatment, and after a follow-up period. Researchers will measure language skills using various tools, including parent and clinician reports and play-based samples. The study also collects qualitative data from parents and clinicians to understand treatment outcomes. The total participation time covers these assessments and imaging sessions, helping to link brain changes with language improvements and treatment effects.

CONDITIONS

Brief Title

Using Neuroimaging and Behavioral Assessments to Understand Late Talking

Who Can Participate

Age: 18Months - 30Months
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Child and parent are primarily monolingual/native English speakers
  • Child is enrolled at one of the participating facilities
  • Child is recruited via word of mouth, including social media
  • Child is between 18 and 30 months of age
  • Child has no contraindications to magnetic resonance imaging (e.g., no intracranial metal implants, no claustrophobia)
  • Child has no uncorrected vision problems
Not Eligible

You will not qualify if you...

  • Child does not meet criteria for late talking or typical development
  • Child meets standard magnetic resonance imaging exclusion criteria
  • Child was born before 37 weeks or after 42 weeks of gestation
  • Child is placed in special education based on ability or behavior

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 to 8 weeks

Participants who are late talkers receive an intervention program designed to support speech and language development, including parent coaching and direct child support, over 6 to 8 weeks.

1 to 2 visits per week

Follow-up

Duration - 8 to 9 weeks

Participants are assessed after the treatment period to measure changes in language and brain connectivity.

1 to 2 visits during follow-up period

Trial Site Locations

Total: 2 locations

1

Grandview Kids

Oshawa, Ontario, Canada, L1H0C8

Actively Recruiting

2

Speech Specialists

Toronto, Ontario, Canada, M1X0C3

Actively Recruiting

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Research Team

K

Karla N Washington, PhD

N

Nicole Bazzocchi, MhSc

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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