Actively Recruiting
Evidence-based Intervention Enhancements to Reduce Language Delays and Disorders Among Children of Parents With Substance Use Disorders
Led by University of Oregon · Updated on 2026-04-20
244
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
Sponsors
U
University of Oregon
Lead Sponsor
N
National Institute on Deafness and Other Communication Disorders (NIDCD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying ways to improve early language development in young children whose parents have substance use disorder (SUD). Children in these families face a higher risk of language delays, and early support may help reduce future learning difficulties. This research evaluates whether adding extra support services to a group-based parenting program enhances children's language skills compared to the group program alone. The study will enroll 244 parent-child pairs and randomly assign them to one of four groups. All parents participate in the "Learn and Play Every Day" group intervention, which meets weekly for six 90-minute sessions led by a trained facilitator using videos and discussion. Some groups will also receive telehealth coaching sessions, individualized lessons, both, or neither. Coaching involves three one-hour sessions with a speech-language pathologist, while individualized lessons focus on practical supports to overcome barriers like attention or memory challenges. Participants will be assessed before the intervention, immediately after (2 months), and at two follow-ups (4 and 8 months). Researchers will video record parent-child interactions and analyze language skills and parental responsiveness. Surveys and interviews will gather information on acceptability and implementation. The main measure is parental responsivity—the number of responses to their child's communication attempts per minute—with child vocabulary and other language outcomes also evaluated. Data on demographics and substance use history will be collected electronically. The study will last about eight months per participant.
CONDITIONS
Brief Title
Prevent Language Delays and Disorders Among Children of Caregivers With Substance Use Disorders With Community Groups and Individualized Services
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be 18 years of age or older
- Have a self-reported lifetime history of substance use disorder treatment or active substance use in the past year
- Be caring for a child between 12 and 42 months old at least 10% of the time
- Child is English or Spanish monolingual or bilingual, exposed to a third language once a week or less
- Child is not regularly combining three or more words and has fewer than 150 words in expressive vocabulary
- Able to provide consent for the child to participate or have a legal guardian provide consent
- Able to speak and understand English and/or Spanish
- Willing to attend weekly group sessions for six weeks and Zoom meetings if assigned additional services
You will not qualify if you...
- Only one caregiver per child can participate; caregivers whose child already has another caregiver enrolled are not eligible
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - 6 weeks
Participants attend six weekly 90-minute group sessions in person and may receive additional telehealth coaching and support sessions depending on their assigned intervention group.
6 weekly group visits (in-person) plus up to 6 telehealth sessions
Duration - 6 months
Participants complete follow-up assessments to measure parent responsivity and child language outcomes at multiple timepoints after treatment.
4 assessment visits at baseline, 2 months, 4 months, and 6 months
Trial Site Locations
Total: 1 location
1
Prevention Science Institute
Eugene, Oregon, United States, 97403
Actively Recruiting
Research Team
S
Stephanie De Anda, PhD, CCC-SLP
M
Maya Casper
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
PREVENTION
Number of Arms
4