Actively Recruiting

Phase 2
Age: 18Months - 48Months
All Genders
Healthy Volunteers
NCT05926687

Optimizing Outcomes for Young Autistic Children

Led by Northwestern University · Updated on 2026-01-29

184

Participants Needed

1

Research Sites

189 weeks

Total Duration

On this page

Sponsors

N

Northwestern University

Lead Sponsor

U

University of Texas at Austin

Collaborating Sponsor

AI-Summary

What this Trial Is About

The overarching goal of the proposed study is to: (a) determine how best to sequence two parent-mediated interventions: a social communication intervention (Project ImPACT, Improving Parents as Communication Teachers) and a disruptive behavior intervention (Parent Training for Disruptive Behavior) and (b) examine moderators and mediators of intervention outcomes.

CONDITIONS

Official Title

Optimizing Outcomes for Young Autistic Children

Who Can Participate

Age: 18Months - 48Months
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Child is between 18 and 48 months old
  • Child scores above the research cutoff for ASD on the TELE-ASD-PEDS
  • Child has no other known diagnosis or disability at study entry
  • Child has normal vision
  • Child is exposed to English at least 50% of the time
  • Child has a caregiver willing to learn the intervention strategies
  • Caregiver wants help supporting their child's social communication and behavior regulation
  • Caregiver understands conversational English well enough to participate in caregiver instruction
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Northwestern University

Evanston, Illinois, United States, 60208

Actively Recruiting

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Research Team

L

Laura J Sudec, MSW

CONTACT

M

Megan Y Roberts, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

6

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