Improving Older Adults' Decision Making for Obstructive Sleep Apnea Treatment (Phase 3)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 36
- 试验地点
- 2
- 主要终点
- Recruitment rates
研究概览
简要总结
This study evaluates the feasibility of conducting a randomized controlled trial that tests a patient decision aid for obstructive sleep apnea in older adults with newly-diagnosed obstructive sleep apnea treated in an outpatient sleep clinic. Half of the participants will use a patient decision aid, while the other half will receive general information about sleep.
详细描述
Patient decision aids are one strategy for helping older adults make informed decisions about treatments. Patient decision aids improve patients' knowledge about therapies and encourage them to actively weigh the risks and benefits of each therapy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 60 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •age >= 60 years
- •diagnosed with obstructive sleep apnea on a sleep study
- •able to read English-language newspaper text (if needed, using contact lens/glasses)
- •able to write words in a paper booklet
- •scheduled for a sleep clinic appointment with a UCLA sleep provider
- •able to attend a sleep educational session prior to sleep clinic appointment
排除标准
- •unable to provide informed consent
- •mild cognitive impairment diagnosis or Mini-Cog score < 3
- •treated for obstructive sleep apnea for > 30 days prior to scheduled sleep education intervention
- •severe physical or mental illness (e.g., hospitalized within past 7 days prior to scheduled sleep education intervention, substance abuse within 90 days of sleep education intervention)
研究组 & 干预措施
Patient decision aid
干预措施: Patient decision aid (Behavioral)
General sleep education
干预措施: General sleep education (Behavioral)
结局指标
主要结局
Recruitment rates
时间窗: Through study completion, an average of 1 year
The investigators will measure recruitment rates for our recruitment strategies
Enrollment rates
时间窗: Through study completion, an average of 1 year
The investigators will measure enrollment rates
次要结局
- The length of time for completing the intervention session(Through study completion, an average of 1 year)
研究者
Constance Fung, MD, MSHS
Principal Investigator
University of California, Los Angeles