Actively Recruiting
Brief Sleep Intervention for Bedtime Resistance
Led by Oregon Health and Science University · Updated on 2026-04-09
40
Participants Needed
1
Research Sites
65 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is non-controlled feasibility study testing the delivery of a brief sleep intervention for children aged 3-7 who struggle to fall asleep independently. The interventions is designed to be delivered by a behavioral health consultant during routine primary care visits. The treatment components consist of education about good sleep hygiene and the "Bedtime Pass." The hypotheses are that the intervention will be delivered with fidelity in the time allotted, and that parents will rate the intervention as feasible and acceptable.
CONDITIONS
Official Title
Brief Sleep Intervention for Bedtime Resistance
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Caregiver of a child aged 3 to 7 years who receives primary care services
- Child demonstrates bedtime resistance
- English-speaking caregiver
- Receiving primary care at the study locations
You will not qualify if you...
- Currently receiving a more intensive sleep intervention
- Severe intellectual disability or other condition that prevents participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Oregon Health & Science University
Portland, Oregon, United States, 97239
Actively Recruiting
Research Team
A
Andrew R Riley, PhD
CONTACT
C
Cassidy McDermott, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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