Prospective Study Evaluating the Use of PROSPECT, a Cognitive Behavioral Therapy-based Internet Module, to Reduce Insomnia in Patients With Early Stage Breast Cancer
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 4
- 试验地点
- 2
- 主要终点
- Change in Insomnia Severity Index
研究概览
简要总结
Women with early stage breast cancer may experience difficulty falling asleep or staying asleep. If this occurs for more than 4 weeks, these participants may have chronic insomnia. Chronic insomnia can lead to difficulty coping with stress, changes in mood, increased use of medications for sleep and an overall decrease in quality of life.
The investigators have developed an internet-based website that is designed to help people manage symptoms typically experienced by breast cancer survivors, including insomnia, fatigue, pain and overall poor quality of life. The investigators want to learn whether this type of treatment can reduce chronic insomnia and improve the way subjects feel using both questionnaires and a special form of a wrist watch. This information may help the investigators better manage sleep difficulties in subjects who experience these symptoms after diagnosis of their breast cancer.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Clinical diagnosis of insomnia as identified through the screening Insomnia Severity Index score >14
- •Insomnia present for > 30 days per patient report
- •Female gender
- •Histologically proven stage 0-III invasive carcinoma of the breast
- •a. Patient's must have completed primary surgical resection at least 2 weeks prior to enrollment, radiation at least 2 weeks prior to enrollment and/or cytotoxic chemotherapy at least 6 weeks prior to enrollment in the study
- •ECOG performance status 0-2
- •Ability to operate the accelerometer (Actiwatch Spectrum Pro)
- •The patient is aware of the nature of her diagnosis, understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent document
排除标准
- •Subjects who do not have access to the internet to use the internet-based module, PROSPECT
- •Initiation of hormone therapy <4 weeks prior to enrollment in the study
- •Initiation of sleep aids, including over-the-counter or prescription medications taken for insomnia (melatonin, benzodiazepines, antihistamines, etc.) for < 4 weeks prior to enrollment in the study
- •Use of medication for treatment of another sleep disorder, such as restless leg syndrome or narcolepsy
- •History of medial or arthritic disease that could confound or interfere with evaluation of activity level, including but not limited to inflammatory arthritis (Rheumatoid Arthritis, Systemic Lupus Spondyloarthropathy, Psoriatic Arthritis, Polymyalgia Rheumatica), Parkinson's disease and cancer involving the bone
- •Second or third shift workers or others with non-traditional sleep schedules
- •Serious or unstable medical condition that could likely lead to hospitalization during the course of the study or compromise study participation
研究组 & 干预措施
PROSPECT
Participants who have received treatment for early stage breast cancer and who experience chronic insomnia as assessed by difficulty sleeping for >30 days with an insomnia severity index score of >14. Participants will complete baseline symptom questionnaires and actigraphy, then complete an internet-based cognitive behavioral therapy program (PROSPECT) for 6 weeks. Participants will then repeat questionnaires and actigraphy at 6 weeks and questionnaires at 12 weeks.
干预措施: PROSPECT (Behavioral)
结局指标
主要结局
Change in Insomnia Severity Index
时间窗: 6 weeks
Insomnia will be measured through the use of a validated survey called the Insomnia Severity Index
次要结局
- Change in Sleep Disturbance as measured by Actigraphy(6 weeks)