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临床试验/NCT00933959
NCT00933959已完成1 期

A Pilot Study of Two Contrasting Intervention Programs for Sleep Management

University of Utah1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2008年3月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
60
试验地点
1
主要终点
Medical Outcomes Study-Sleep Scale

研究概览

简要总结

The aim of the proposed pilot study is to scientifically evaluate the use of Mind-Body Bridging Program (MBBP) as an effective intervention for improving health outcomes in veterans exhibiting sleep disturbance in the Primary Care Clinic at the Veterans Administration Salt Lake City Health Care System (VASLCHCS).

详细描述

Participants will be randomly assigned to either MBBP or a treatment as usual sleep hygiene (SH) group. The interventions will last two weeks in which participants will attend 2 classes 1-1.5 hr each over two consecutive weeks. Assessment of the effects of the treatments will be based on self-report outcome measures; participants will complete five questionnaires approximately one week prior to the start of the interventions (pre-treatment) and one week after the second session (post-treatment). The sleep quality assessment questionnaire will be additionally completed after the first session (Week 1).

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
Single (Participant)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Selection of subjects will be based on the patients exhibiting sleep disturbance as assessed by a standardized sleep questionnaire. Because we are also interested in the effects of MBBP on co-morbid illnesses besides insomnia, we will include subjects that are being treated for depression, pain, and general medical conditions, except as defined as

排除标准

  • . Subjects using anti-depressants, sleep and pain medications, and other medications for any condition that is not under exclusion criteria will be admitted to the study. Thus our inclusion criteria will be broader than those based on DSM-IV for primary insomnia.
  • On the day of the study session, patients must arrive before the session for intervention assignment and to turn in their packets, and thereafter on the same day they must be able to attend a mind-body bridging program or sleep hygiene class (see Study Procedure). In addition, they must also be able to attend the second session the following week.
  • Exclusion Criteria:
  • The patient presents with significant mental health issues, such as severe psychosis or major depression (as verified by the primary care provider) or the patient is under intensive mental health case management.

研究组 & 干预措施

Mind-Body Bridging Program

Experimental

Subjects will undergo two approximately 1.5 hr training sessions using MBBP spaced one week apart at the VASLCHCS. Each training session will comprise a number of objectives:

Session 1:

  1. The patient will discover the underlying cause of the insomnia.
  2. The patient will learn how to use easy to apply tools to quieten the mind to sleep soundly.

Session 2:

  1. The patient will learn how to reduce daytime stress.
  2. The patient will experience a greater sense of self.

To be maximally effective, the participant should master these objectives and practice MBBP on a daily basis. Bridging and all the other MBBP techniques can be implemented at any time throughout the day and right up to the onset of sleep.

干预措施: Mind-Body Bridging Program (Behavioral)

Sleep Hygiene

Active Comparator

Participants in the sleep hygiene arm will receive a 1 hr class directing them to the importance of following a list of up to 15 points (tips) for getting to sleep. These points include: limiting alcohol and caffeine intake before bed, using the bed only for sleeping, and having regular bedtimes. Once the instructor has gone over this list and has described in detail each of the 15 points, the class will have an opportunity to ask questions. The participant will be encouraged to learn and practice the objectives of the sleep hygiene class on a daily basis.

干预措施: Sleep Hygiene (Behavioral)

结局指标

主要结局

Medical Outcomes Study-Sleep Scale

时间窗: Pre-treatment, Week 1, Post treatment

Medical Outcomes Study Short Form-36 for Veterans

时间窗: Pre-treatment, Post treatment

次要结局

  • Center for Epidemiologic Studies Depression Scale(Pre-treatment, Post treatment)
  • Five-factor Mindfulness Questionnaire(Pre-treatment, Post treatment)
  • PTSD Check List-Military(Pre-treatment, Post treatment)

研究者

申办方类型
Other

研究点 (1)

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