跳至主要内容
临床试验/NCT01042587
NCT01042587
已完成
不适用

Effect of Bright Light Treatment On Elders In A Long Term Care Environment

Milton S. Hershey Medical Center1 个研究点 分布在 1 个国家目标入组 32 人2010年3月

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Behavioral Responses to Bright Light Therapy in Elders
发起方
Milton S. Hershey Medical Center
入组人数
32
试验地点
1
主要终点
assessment of cognitive functioning using MicroCog
状态
已完成
最后更新
15年前

概览

简要总结

The investigators hypothesize that significant exposure to artificial morning bright light (approximately 200 lux of primarily blue light at eye level for thirty minutes daily) as compared to sham bright red light (placebo) will:

  1. improve sleep quality
  2. improve cognitive scores
  3. improve depression scores
  4. improve quality of life scores.

详细描述

Bright light therapy has been shown to improve depression and insomnia in multiple studies. These are common conditions among elders, particularly those residing in long term care environments. Bright light therapy has been inadequately studied in the geriatric population. We will show that a groups of twenty elders can simultaneous be exposed to bright light and that it will result in improvements in multiple realms of behavior and quality of life. Elders will be tested with a number of neuropsychological test batteries prior to exposure to bright light and again at the end of a four week exposure. Some subjects will have daytime and night time activity levels monitored with actigraphy. Cortisol and melatonin levels will be obtained prior to and at the end of the exposure period.

注册库
clinicaltrials.gov
开始日期
2010年3月
结束日期
2010年6月
最后更新
15年前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

入排标准

入选标准

  • residents in Masonic Villages, Elizabethtown, PA long term care
  • ability to give informed consent and complete the neuropsychological tests

排除标准

  • blindness
  • severe illness expected to preclude the ability to complete treatment
  • moderate to severe dementia that precludes the ability to complete testing
  • light sensitivity making treatment to light therapy uncomfortable

结局指标

主要结局

assessment of cognitive functioning using MicroCog

时间窗: once prior to intervention, once near the end of intervention, once four weeks after intervention

Assessment of mood using the Geriatric Depression Scale

时间窗: once prior to intervention, once near the end of intervention, once four weeks after intervention

assessment of quality of life using the SF-36

时间窗: once prior to intervention, once near the end of intervention, once four weeks after intervention

assessment of sleep quality using the Pittsburgh Sleep Quality Index

时间窗: once prior to intervention, once near the end of intervention, once four weeks after intervention

assessment of mood using the Profile of Moods Survey

时间窗: weekly throughout the duration of the study

assessment of sleep quality using the Epworth Sleepiness Scale

时间窗: weekly throughout the duration of the study

day and nightime activity level (5 subjects per group only) using Actigraphy

时间窗: two weeks prior to light exposure and the second two weeks during light exposure (continuous measurements)

次要结局

  • salivary melatonin levels(once prior and near the end of light exposure period)
  • salivary cortisol levels(once prior and near the end of light exposure period)

研究点 (1)

Loading locations...

相似试验