跳至主要内容
临床试验/NCT05759065
NCT05759065招募中不适用

A Hybrid Effectiveness Implementation Trial Evaluating Behavioral Treatments for Insomnia for Socioeconomically Disadvantaged Adults in Primary Care

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 350 人开始时间: 2024年4月2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
350
试验地点
1
主要终点
Insomnia severity index, ISI

研究概览

简要总结

The overall objective of this study is to conduct a randomized effectiveness-implementation trial to test the non-inferiority of tele-Brief Behavioral Treatment for Insomnia vs. tele-Cognitive-Behavioral Therapy for Insomnia among socioeconomically disadvantaged adults with insomnia in the primary care setting.

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
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
否

入选标准

  • •Aged 18 years or older
  • •Meet clinical diagnostic criteria for insomnia (DSM-V criteria)
  • •Insomnia severity score > 10
  • •Eligible to receive care through publicly-supported medical assistance (e.g. Commonwealth Connector plan; MassHealth. For participants >65 years old on Medicare, they will be asked about insurance coverage prior to initiating Medicare, OR
  • •Identify as racial or ethnic minority
  • •Has capacity for informed consent (SDT<9)

排除标准

  • •Untreated, current major depressive disorder (PHQ-8≥ 20)
  • •History of bipolar disorder or psychosis
  • •Active alcohol abuse (Alcohol Use Disorders Identification Test, AUDIT-C) or drug abuse (Drug Abuse Screening Test, DAST-2 ≥1)
  • •Excessive daytime sleepiness (Epworth Sleepiness Scale score ≥ 16)
  • •Seizure within the past 1 year
  • •Main sleep period outside of 8pm - 11am
  • •Regular nightshift work (5 overnight shifts/month, defined as working between midnight-5am)
  • •Untreated, previously diagnosed moderate to severe sleep apnea
  • •Severe medical condition, which may require hospitalizations over the next 6 months
  • •Active suicidal ideation, if elicited passively during screening
  • •Pregnant or planning to become pregnant (self-reported)
  • •Participation in other studies that may impact the benefit or safety of the intervention, as determined by the study PI

研究组 & 干预措施

Tele-Brief Behavioral Treatment for Insomnia

Experimental

干预措施: Tele-Brief Behavioral Treatment for Insomnia (Behavioral)

Tele-Cognitive-Behavioral Therapy for Insomnia

Active Comparator

干预措施: Tele-Cognitive-Behavioral Therapy for Insomnia (Behavioral)

结局指标

主要结局

Insomnia severity index, ISI

时间窗: 3 months

The Insomnia Severity Index is a 7-item self-report questionnaire assessing the nature, severity, and impact of insomnia in the last month. A 5-point Likert scale is used to rate each item (e.g., 0 = no problem; 4 = very severe problem), yielding a total score ranging from 0 to 28. The total score is interpreted as follows: absence of insomnia (0-7); sub-threshold insomnia (8-14); moderate insomnia (15-21); and severe insomnia (22-28).

次要结局

  • Diary reported sleep duration(3-months)
  • Quality of Life and Symptoms - Generic-quality of life(3-months)
  • Generalized Anxiety Disorder (GAD-7)(3-months)
  • Number of participants with hypnotic use self-reported from the sleep diary(3-months)
  • Quality of Life and Symptoms - Patient-Reported Outcomes Measurement Information System (PROMIS) Global Health(3-months)
  • Patient Health Questionnaire for depression (PHQ-8)(3-months)
  • Patient-Reported Outcomes Measurement Information System (PROMIS) Sleep Impairment, 8a(3-months)
  • Patient-Reported Outcomes Measurement Information System (PROMIS) Sleep Disturbance, 8b(3-months)
  • Diary-reported sleep efficiency(3-months)
  • Insomnia severity index, ISI(6- and 12-months)

研究者

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

Suzanne M. Bertisch, MD, MPH

Associate Physician, Clinical Director of Behavioral Sleep Medicine

Brigham and Women's Hospital

研究点 (1)

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