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临床试验/NCT05016219
NCT05016219招募中不适用

Phase 2 - The Use of Rhythmic Light Therapy to Entrain Gamma Oscillations and the Circadian System in Patients With Alzheimer's Disease

Icahn School of Medicine at Mount Sinai2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2023年8月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
120
试验地点
2
主要终点
Cognition using the Montreal Cognitive Assessment (MoCA)

研究概览

简要总结

Participants will randomly be placed into one of four groups and experience one of the four following conditions: (1) a placebo light that provides a 40 hertz (Hz) flicker (rhythmic light [RL]); (2) a placebo light with a random flicker (placebo condition for rhythmic light); (3) a light source that will stimulate the circadian system and provides a 40 Hz flicker (RL); or (4) a light source that will stimulate the circadian system and provides a random flicker (placebo condition for rhythmic light). Following a baseline week, participants will experience his/her assigned lighting condition for two hours in the morning for 8 weeks. After a 4-week washout period, a final round of assessments will be obtained. Study assessments (except for the Pittsburgh Sleep Quality Index and Montreal Cognitive Assessment) will be collected at the end of each week, for a total of 8 assessments.

详细描述

The tailored lighting intervention used to promote circadian entrainment will provide high circadian stimulation during the day produced by narrowband blue light peaking at 470 nanometers (nm). A comparison lighting intervention (i.e., placebo lighting), a narrowband red light peaking at 630 nm, will be used as a control. Both the red and the blue light devices will also provide either the 40 hertz (Hz) flicker (RL) or the random flicker (placebo RL). For the random flicker (placebo RL), the duty cycle will be delivered with a random interval determined by a Poisson process with an average interval of 40 hertz (Hz).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • •Participants must be diagnosed with mild cognitive impairment or mild Alzheimer's disease, as defined by a Montreal Cognitive Assessment score between 17 and 25;
  • •Have sleep disturbance indicated by a score >5 on the Pittsburgh Sleep Quality Index
  • •Participants must reside in their homes, independent living, or assisted living facilities

排除标准

  • •Participants taking sleep medication
  • •Residence in a skilled nursing facility or long-term care
  • •Obstructing cataracts, macular degeneration, and blindness
  • •Severe sleep apnea or restless leg syndrome
  • •History of severe epilepsy

研究组 & 干预措施

Active Intervention plus Active Rhythm

Active Comparator

The device will set on a tabletop in a room where the participant spends at least 2 hours in the morning. Using a timer, it will automatically turn on at preferred wakeup times (but no later than 09:00 am) chosen by the participant. Lights will remain on for at least 2 hours and participants will be asked to remain the space that lights are being applied for that period of time.

干预措施: Circadian-Effective Light (Device)

Active Intervention plus Active Rhythm

Active Comparator

The device will set on a tabletop in a room where the participant spends at least 2 hours in the morning. Using a timer, it will automatically turn on at preferred wakeup times (but no later than 09:00 am) chosen by the participant. Lights will remain on for at least 2 hours and participants will be asked to remain the space that lights are being applied for that period of time.

干预措施: Rhythmic Light (Device)

Active Light plus Placebo Rhythm

Active Comparator

The device will set on a tabletop in a room where the participant spends at least 2 hours in the morning. Using a timer, it will automatically turn on at preferred wakeup times (but no later than 09:00 am) chosen by the participant. Lights will remain on for at least 2 hours and participants will be asked to remain the space that lights are being applied for that period of time.

干预措施: Circadian-Effective Light (Device)

Active Light plus Placebo Rhythm

Active Comparator

The device will set on a tabletop in a room where the participant spends at least 2 hours in the morning. Using a timer, it will automatically turn on at preferred wakeup times (but no later than 09:00 am) chosen by the participant. Lights will remain on for at least 2 hours and participants will be asked to remain the space that lights are being applied for that period of time.

干预措施: Placebo Rhythmic Light (Device)

Placebo Light plus Active Rhythm

Active Comparator

The device will set on a tabletop in a room where the participant spends at least 2 hours in the morning. Using a timer, it will automatically turn on at preferred wakeup times (but no later than 09:00 am) chosen by the participant. Lights will remain on for at least 2 hours and participants will be asked to remain the space that lights are being applied for that period of time.

干预措施: Rhythmic Light (Device)

Placebo Light plus Active Rhythm

Active Comparator

The device will set on a tabletop in a room where the participant spends at least 2 hours in the morning. Using a timer, it will automatically turn on at preferred wakeup times (but no later than 09:00 am) chosen by the participant. Lights will remain on for at least 2 hours and participants will be asked to remain the space that lights are being applied for that period of time.

干预措施: Placebo Light (Device)

Placebo Light plus Placebo Rhythm

Placebo Comparator

The device will set on a tabletop in a room where the participant spends at least 2 hours in the morning. Using a timer, it will automatically turn on at preferred wakeup times (but no later than 09:00 am) chosen by the participant. Lights will remain on for at least 2 hours and participants will be asked to remain the space that lights are being applied for that period of time.

干预措施: Placebo Light (Device)

Placebo Light plus Placebo Rhythm

Placebo Comparator

The device will set on a tabletop in a room where the participant spends at least 2 hours in the morning. Using a timer, it will automatically turn on at preferred wakeup times (but no later than 09:00 am) chosen by the participant. Lights will remain on for at least 2 hours and participants will be asked to remain the space that lights are being applied for that period of time.

干预措施: Placebo Rhythmic Light (Device)

结局指标

主要结局

Cognition using the Montreal Cognitive Assessment (MoCA)

时间窗: at the end of week 14

The Montreal Cognitive Assessment is a one-page, 30-point test that can be administered in 10 minutes. It assesses short-term memory, visuospatial abilities, executive functions, attention, concentration and working memory, language, and orientation to time and place. total score ranging from 0 to 30 units on a scale, with higher score indicating better cognitive global function.

Cognition using the Montreal Cognitive Assessment (MoCA)

时间窗: baseline

The Montreal Cognitive Assessment is a one-page, 30-point test that can be administered in 10 minutes. It assesses short-term memory, visuospatial abilities, executive functions, attention, concentration and working memory, language, and orientation to time and place. total score ranging from 0 to 30 units on a scale, with higher score indicating better cognitive global function.

Cognition using the Montreal Cognitive Assessment (MoCA)

时间窗: at the end of week 9

The Montreal Cognitive Assessment is a one-page, 30-point test that can be administered in 10 minutes. It assesses short-term memory, visuospatial abilities, executive functions, attention, concentration and working memory, language, and orientation to time and place. total score ranging from 0 to 30 units on a scale, with higher score indicating better cognitive global function.

次要结局

  • Cognition using a word pair associates task(at the end of week 14.)
  • Cognition using an implicit priming task(at the end of week 14.)
  • Cognition using the Alzheimer's Disease Assessment Scale - Cognitive Subscale(at the end of week 14.)
  • Sleep Quantity using Actigraphy(week 14)
  • Urine Melatonin Biomarker(at the end of week 9.)
  • Sleep Quality using the Pittsburgh Sleep Quality Index (PSQI)(at the end of week 14.)
  • Quality of Life using the Dementia Quality of Life Instrument(at the end of week 14.)
  • Cognition using a working memory task(at the end of week 14)
  • Light Exposure using a Daysimeter(week 14.)
  • Cognition using a working memory task(baseline)
  • Cognition using a working memory task(at the end of week 9)
  • Cognition using a word pair associates task(baseline)
  • Cognition using a word pair associates task(at the end of week 9)
  • Cognition using an implicit priming task(baseline)
  • Cognition using an implicit priming task(at the end of week 9)
  • Cognition using the Alzheimer's Disease Assessment Scale - Cognitive Subscale(baseline)
  • Cognition using the Alzheimer's Disease Assessment Scale - Cognitive Subscale(at the end of week 9)
  • Urine Melatonin Biomarker(baseline)
  • Light Exposure using a Daysimeter(baseline)
  • Light Exposure using a Daysimeter(week 9)
  • Sleep Quantity using Actigraphy(baseline)
  • Sleep Quantity using Actigraphy(week 9)
  • Sleep Quality using the Pittsburgh Sleep Quality Index (PSQI)(baseline)
  • Sleep Quality using the Pittsburgh Sleep Quality Index (PSQI)(at the end of week 9)
  • Quality of Life using the Dementia Quality of Life Instrument(baseline)
  • Quality of Life using the Dementia Quality of Life Instrument(at the end of week 9)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mariana Figueiro

Professor, Population Health Science and Policy

Icahn School of Medicine at Mount Sinai

研究点 (2)

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