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临床试验/NCT04468776
NCT04468776已完成4 期

Comparative Effectiveness of Zolpidem/Trazodone and Cognitive Behavioral Therapy for Insomnia in Rural Adults

California Pacific Medical Center Research Institute7 个研究点 分布在 1 个国家目标入组 155 人开始时间: 2022年2月25日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
155
试验地点
7
主要终点
Change in Insomnia Symptom Severity

研究概览

简要总结

This study is a randomized (1:1:1) comparative effectiveness trial of medication (zolpidem or trazodone), cognitive-behavioral therapy for insomnia (CBT-I), and the combination (medication + CBT-I) for the treatment of chronic insomnia in men and women aged 18-80 living in rural areas with 1 year of follow-up. A total of 155 participants will be enrolled and randomized in the United States. This trial is funded by the Patient-Centered Outcomes Research Institute.

详细描述

Insomnia is a common health problem that causes distress, impaired function, and increased risk for other health problems. Chronic insomnia is defined by problems with the quality or amount of sleep, including difficulty falling asleep, frequent awakenings, and/or awakening early and being unable to return to sleep. In developing this application, patients, providers, payors, and the investigators identified both concerns and opportunities with current treatments for chronic insomnia. Medications and Cognitive-Behavioral therapy for insomnia (CBT-I; a treatment program to improve sleep through changes in behavior and thinking) are both effective for treating insomnia. Zolpidem, the most frequently prescribed insomnia medication, is widely available, but may cause side effects and dependency. Trazodone is increasingly prescribed off-label for treatment of insomnia, but evidence of efficacy and safety is more limited. CBT-I is the recommended first line treatment by many professional organizations, but it is not widely available in physicians' practices. Patients, providers, and payors face important unanswered questions: Which treatment should be used for the treatment of chronic insomnia? Is combination therapy more effective, and does it result in lower zolpidem use? Who responds best to which treatment? These dilemmas are particularly relevant to patients and providers in rural areas, where access to behavioral health specialists is limited, and concerns regarding use of controlled substances is particularly acute.

To address these questions, we propose the study, Comparative Effectiveness of Zolpidem/Trazodone and Cognitive Behavioral Therapy for Insomnia in Rural Adults (COZI). The investigators will use a well-tested Internet version of CBT-I, which is just as effective as in-person CBT-I, but more widely available. The aims of COZI are to: 1: Compare the effectiveness of medication preference (zolpidem or trazodone), CBT-I, and combination treatment for insomnia symptoms over 6 months. 2: Compare the effectiveness of medication preference, CBT-I, and combination treatment for other symptoms and problems, including health-related quality of life, mood, and health outcomes. 3: Compare the side effects of medication preference, CBT-I, and combination treatment. COZI will study 155 patients recruited from 7 health care systems across the country, each of which has established practices in rural areas. Patients will be treated with medication prescribed by their own physician (zolpidem or trazodone), Internet CBT-I, or a combination of the two. The investigators will evaluate treatment effects at 9 weeks, and 6 and 12 months (with limited additional assessments for adverse events and medication use at 1 and 9 months). Our study questions and design reflect early and ongoing engagement of key stakeholders including patients, providers, and payors, who are members of the Study Advisory Committee (SAC). SAC members will work with study investigators to recommend the best strategies for recruiting patients, measuring treatment effects, and disseminating study findings. The SAC will meet quarterly. Patients and other stakeholders have already provided guidance on which treatments are most worth studying, and which symptoms would best reflect the effects of treatment. Patients and other stakeholders will also be part of the Steering Committee, which is the main decision-making group for our study, and which will meet monthly. COZI will lead to answers for patients and providers addressing insomnia; improved health and function for millions of rural Americans; and sustainable changes in how insomnia is treated in rural practices.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

盲法说明

Masking of participants and providers is not possible given two very different treatment types. The Prime Principal Investigator and a statistician at the Data Coordinating Center will be masked to individual treatment assignment.

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-80
  • Insomnia Severity Index score > 10
  • Regular internet and computer access
  • Receives primary care in a Non-metropolitan/Rural residence

排除标准

  • Use of hypnotic medication >2 times in the past week
  • Current cognitive or cognitive behavioral treatment for insomnia
  • Psychotic disorder
  • Bipolar disorder
  • Current substance use disorder
  • Severe Chronic obstructive pulmonary disease (COPD) or other severe pulmonary disease (such as asthma or lung fibrosis)
  • Cognitive impairment or dementia
  • History of spontaneous or hypnotic-induced complex sleep behavior
  • Delayed sleep phase disorder (DSPD)
  • Shift work that includes working the night shift (between the hours of 12:00 a.m. - 6:00 a.m.)
  • History of fracture or injurious fall in the past 12 months
  • Currently pregnant, planning to become pregnant, or breastfeeding
  • Other severe or uncontrolled mental or physical disorders that would make participation difficult or unsafe

研究组 & 干预措施

Medication (zolpidem or trazodone)

Active Comparator

Zolpidem or trazodone, as prescribed by physician

干预措施: Zolpidem (Drug)

Medication (zolpidem or trazodone)

Active Comparator

Zolpidem or trazodone, as prescribed by physician

干预措施: Trazodone (Drug)

Internet Cognitive Behavioral Therapy for Insomnia (CBT-I)

Active Comparator

Internet-based CBT-I program

干预措施: Internet Cognitive Behavioral Therapy for Insomnia (CBT-I) (Behavioral)

Combination

Experimental

Medication (zolpidem or trazodone) as prescribed by physician and Internet-based CBT-I program

干预措施: Zolpidem (Drug)

Combination

Experimental

Medication (zolpidem or trazodone) as prescribed by physician and Internet-based CBT-I program

干预措施: Internet Cognitive Behavioral Therapy for Insomnia (CBT-I) (Behavioral)

Combination

Experimental

Medication (zolpidem or trazodone) as prescribed by physician and Internet-based CBT-I program

干预措施: Trazodone (Drug)

结局指标

主要结局

Change in Insomnia Symptom Severity

时间窗: Baseline, 6 months

Change in Insomnia Severity Index score from baseline to follow-up. The Insomnia Severity Index is a 7-item self-report questionnaire that measures severity of insomnia symptoms during the last two weeks. Each item is scored 0 (no problem) to 4 (very severe problem) and total between 0-28, with higher scores indicating more severe insomnia symptoms. Change is estimated mean change from mixed-effects linear regression model. Fixed effects: Baseline ISI, Treatment Arm, Visit and Treatment Arm\*Visit interaction. Random effects: intercept for Subject, nested within Site.

次要结局

  • Number of Participants With Treatment Response of Insomnia Symptoms(Baseline, 6 months)
  • Number of Participants With Remission of Insomnia Symptoms(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (7)

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