Brief Sleep Intervention for Bedtime Resistance
Not Applicable
Not yet recruiting
- Conditions
- Child Sleep
- Registration Number
- NCT06970392
- Lead Sponsor
- Oregon Health and Science University
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
- Caregiver of a child aged 3-7 years who receives primary care services who endorses their child demonstrating bedtime resistance; English-speaking; receiving primary care at the study locations.
Exclusion Criteria
- Existing receipt of more intensive sleep intervention; severe intellectual disability or other condition precluding participation.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Acceptability Survey Immediately post-intervention and 30 days post-intervention Treatment Fidelity Checklist Immediately post-intervention
- Secondary Outcome Measures
Name Time Method Pediatric Insomnia Severity Index 30 days post-intervention