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临床试验/NCT06970392
NCT06970392招募中不适用

Brief Sleep Intervention for Bedtime Resistance

Oregon Health and Science University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年5月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Acceptability Survey

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • Existing receipt of more intensive sleep intervention; severe intellectual disability or other condition precluding participation.

研究组 & 干预措施

Bedtime Pass

Experimental

The behavioral health consultant will converse with the participant about the child's bedtime resistance, bedtime routine, and other variables that may impact sleep. The behavioral health consultant will provide psychoeducation on sleep hygiene and provide relevant handouts. The behavioral health consultant will also explain the Bedtime Pass Intervention and provide relevant materials. The participant will have the opportunity to ask questions about implementing the intervention at home with their child.

干预措施: Bedtime Pass (Behavioral)

结局指标

主要结局

Acceptability Survey

时间窗: Immediately post-intervention and 30 days post-intervention

Treatment Fidelity Checklist

时间窗: Immediately post-intervention

次要结局

  • Pediatric Insomnia Severity Index(30 days post-intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Andrew Riley

Associate Professor

Oregon Health and Science University

研究点 (1)

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