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临床试验/NCT05978934
NCT05978934招募中不适用

Determining How Indoor Lighting Affects the Brain Health of Older Adults

Well Living Lab, Inc.2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2023年5月15日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
70
试验地点
2
主要终点
Wake After Sleep Onset

研究概览

简要总结

The goal of this randomized, cross-over, single-site trial followed by an exploratory third intervention is to understand how indoor lighting affects different measures of brain health in older adults living in independent living residences. This is a community based study occurring in a local senior living facility. The main question this study aims to answer is:

  • How does the quality of ambient indoor lighting an older adult is exposed to affect measures of brain health, such as sleep quality, physical activity, cognitive function, and social engagement?

Participants will be exposed to three different indoor lighting conditions for 4 weeks each while performing the following tasks:

  • Wear a smartwatch throughout the study to measure sleep quality and physical activity
  • Wear a small, wearable light sensor to measure light exposure during waking hours
  • Perform cognitive assessments throughout the study to detect any changes between each of the lighting conditions
  • Complete self-report of surveys to assess independence, social engagement, sleep quality, and mood

Results from these tasks will be compared within and between subjects to assess whether the different lighting conditions affect these different measures of brain health.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • At least age 60;
  • Able to wear wearable devices throughout the study;
  • Willing to have their lighting in their kitchen and dining areas changed and controlled for the study;
  • Willing to have environmental sensors placed in their residence;
  • Willing to provide contact information about their primary care provider (PCP); and
  • Able and has capacity to provide informed consent (score > 14.5 based on UBACC consent capacity form).

排除标准

  • Is legally blind
  • Previously renovated their living units and no longer have the standard lighting installation offered by the Senior Living Facility;
  • Currently spend or plan to spend most of their day outside of their residence during the study (i.e., would not experience the indoor lighting intervention for the majority of the study);
  • Plan to travel to a different time zone during the study; or
  • Plan to be away from their residence for more than a week during the study.

结局指标

主要结局

Wake After Sleep Onset

时间窗: Change in wake after sleep onset per night over the course of each condition of the 16-week study.

Wake after sleep onset per night in minutes as measured daily by a wearable device.

Total Sleep Time

时间窗: Change in total sleep time per night over the course of each condition of the 16-week study.

Total sleep time per night in minutes as measured daily by a wearable device.

Sleep State Duration

时间窗: Change in sleep state duration per night over the course of each condition of the 16-week study.

Sleep state duration per night in minutes as measured daily by a wearable device.

次要结局

  • Self-Reported Loneliness(Change in self-reported loneliness over the course of each condition of the 16-week study.)
  • Self-Reported Depression(Change in self-reported depression over the course of each condition of the 16-week study.)
  • Sleep Quality(Change in self-reported sleep quality over the course of each condition of the 16-week study.)
  • Steps Taken(Change in physical activity in steps per day over the course of each condition of the 16-week study.)
  • Physical Activity(Change in physical activity in minutes per day over the course of each condition of the 16-week study.)
  • Sustained-Attention Reaction Time(Change in sustain-attention reaction time performance over the course of each condition of the 16-week study.)
  • Self-Reported Mood(Change in self-reported mood over the course of each condition of the 16-week study.)
  • Working Memory(Change in working memory performance over the course of each condition of the 16-week study.)
  • Task Switching(Change in task switching performance over the course of each condition of the 16-week study.)
  • Response Inhibition(Change in response inhibition performance over the course of each condition of the 16-week study.)

研究者

发起方
Well Living Lab, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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