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临床试验/NCT00587340
NCT00587340已完成不适用

A Survey of Sleep Problems in Survivors of Breast Cancer

Memorial Sloan Kettering Cancer Center1 个研究点 分布在 1 个国家目标入组 256 人开始时间: 2006年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
256
试验地点
1
主要终点
Determine the prevalence of cancer-related insomnia in women surviving breast cancer (Stage I, II, & III) who are at least one year, but not more than 10 years posttreatment & to study its deleterious impact on qol

研究概览

简要总结

The purpose of this study is to gain greater understanding of the problems breast cancer survivors experience related to difficulty sleeping and insomnia. Poor sleep can affect a person's mood, increase feelings of fatigue, as well as pain. A greater knowledge and understanding of sleep disturbances can lead to more effective treatment of sleep problems and significantly improve quality of life.

详细描述

Individuals who consent to participate in this study will be asked to complete a battery of questionnaires that will take approximately 1 hour. Based on answers they give to the questionnaires, 45 patients will be asked to participate in a sleep study done at a sleep lab.

If you choose to take part, then you will be asked to do the following:

Spend approximately 1 hour answering questionnaires either at the breast cancer center with a research assistant, at home on the phone with a research assistant, or by completing the questionnaires at home and returning them by mail. You will only be asked to complete questionnaires one time. The questionnaires will ask you questions about your:

  • Past medical history
  • Demographics
  • Sleep quality
  • Sleep habits
  • Energy level, pain, daytime sedation
  • Quality of life
  • Menopausal symptoms
  • Depression
  • Fears

If you are then selected to participate in the sleep study, further information will be provided for you.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Subject Inclusion Criteria for Questionnaire Portion of Study
  • Women with a diagnosis of Stage I, II, or III breast cancer who are one year posttreatment, but not more than 10 years post-treatment (surgery, chemotherapy, and/or radiation) prior to entrance into the study. Use of biological and/or hormonal therapy is acceptable.
  • Greater than 18 years of age.
  • Able to speak and read English.

排除标准

  • Subject Exclusion Criteria for Questionnaire Portion of Study •Evidence of acute or chronic encephalopathy or psychiatric disease severe enough to compromise data collection.
  • Exclusion Criteria for Sleep Lab Study
  • Women who are unable or unwilling to avoid alcohol, caffeine consumption or cigarette smoking as of 3 p.m. on the day of the sleep study.

结局指标

主要结局

Determine the prevalence of cancer-related insomnia in women surviving breast cancer (Stage I, II, & III) who are at least one year, but not more than 10 years posttreatment & to study its deleterious impact on qol

时间窗: 2 years

To describe the underlying physiology and nature of sleep disturbances in this cohort of women by performing sleep lab studies with a subset of the sample

时间窗: 2 years

次要结局

  • To survey the medical, demographic and psychosocial correlates of cancer-related insomnia in this cohort of women to identify subgroups with potentially differing etiologies and associated symptoms to help plan relevant intervention studies(2 Years)
  • To preliminarily describe correlations between subgroups and sleep disturbances documented in the sleep lab studies(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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