Feasibility of Bright Light Therapy on Fatigue, Sleep and Circadian Activity Rhythms in Lung Cancer Survivors
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 14
- 试验地点
- 1
- 主要终点
- Study Completion
研究概览
简要总结
The purpose of this study is to determine the feasibility of a morning bright light therapy intervention for fatigue, sleep disturbances, and circadian activity rhythms in lung cancer survivors.
详细描述
A randomized controlled trial to test the effects of morning bright light therapy on fatigue, sleep disturbances, and circadian activity rhythms in lung cancer survivors.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Device Feasibility
- 盲法
- Single (Participant)
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
- •Stage I-III Non-small cell lung cancer survivors
- •Must be at >6-weeks and < 3 years post-surgical resection
- •Must have diagnosis fatigue and/or sleep disturbances
排除标准
- •Individuals clinically unstable.
- •Mania, Bipolar disease or seizure disorder
- •Macular degeneration or glaucoma.
- •Currently receiving chemotherapy or radiation.
研究组 & 干预措施
Experimental
Exposure to morning bright light therapy delivered with Green-Blue Re-Timer glasses for 30 minutes in the morning during one week.
干预措施: Morning bright light therapy (Device)
Attention Control
Exposure to dim light delivered with Red-Yellow Re-Timer glasses for 30 minutes in the morning during one week.
干预措施: Dim light (Device)
结局指标
主要结局
Study Completion
时间窗: Baseline
The percentage of participants recruited that completed the study
次要结局
未报告次要终点
研究者
Carleara Weiss
Principal Investigator
State University of New York at Buffalo