ALZLIGHT Stage III - Study on the Effect of 40 Hz Non-Invasive Light Therapy System
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 62
- 试验地点
- 2
- 主要终点
- Gamma oscillations assessment
研究概览
简要总结
The ALZLIGHT STAGE III Study is a continuation of the ALZLIGHT Pilot - Study on Safety, Feasibility and Neural Activation of Non-Invasive Light Therapy System. As with the first two stages, this study will examine whether entrainment of 40 Hz neural oscillation by novel 40 Hz Invisible Spectral Flicker is a potential therapy for Alzheimer's Disease. In order to examine this, 62 patients with mild to moderate Alzheimer's Disease will be recruited. The patients will be exposed to the Non-Invasive Light Therapy System for 1 hour a day for 6 months. The effect will be measured by a combination of electroencephalography, cognitive testing, functional magnetic resonance imaging, magnetic resonance spectroscopy and actigraphy.
详细描述
Recent studies in mouse models of Alzhimer's Disease (AD) have shown that exposure to 40 Hz stroboscopic light therapy for one hour a day, resulted in slowing disease progression and lead to multiple neuroprotective effects such as cognition and memory recovery, and even scavenged both tau and Aβ protein species. Hence, the 40 Hz stroboscopic light therapy has a considerable potential for treatment of humans.
This study will utilize a novel way of masked light by alternating the spectral composition of a white light, rendering the flicker invisible to the conscience perception, while still entraining 40 Hz oscillations in the brain.
In the study, 62 patients with probable mild to moderate AD will be exposed to either invisible spectral flickering light through the Light Therapy System (LTS) (active setting) or continuous non-flickering white light (sham setting) for 1 hour each day. The sham setting is a high quality sham intervention as subjects will be blinded to the setting, both appear as white light.
The study will last 8½ months for each participant and consist of 3 periods: Enrollment period of 1 month, an intervention period of 6 months, and a 1½ month post-interventional follow-up period.
In order to test whether the LTS intervention is a potential treatment for AD, cognition will be measured by neuropsychological tests at baseline and at follow-ups. To get a better understanding of the potential effects, markers of efficacy based on MRI, MRS, EEG and blood samples will be tested.
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
- Triple (Participant, Investigator, Outcomes Assessor)
盲法说明
Double-blinded
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
- •Adult competent person, able to understand the nature of the study and give written informed consent.
- •Diagnosed with probable mild to moderate AD based on NIA-AA diagnostic criteria.
- •Age > 55 years. Females must be post-menopausal.
- •Fluent in Danish.
- •> 8 years of normal school education
- •Pass a color-blindness test (Ishihara color test)
- •Have visual and auditory capabilities, and language skills necessary for neuropsychological testing.
- •Participants must have a designated caregiver, who is available to the participant and can provide the necessary assistance with using the LTS device and the Actigraph wearable at home and assist with clinical visits and other practical issues
排除标准
- •Profound visual impairment (visual acuity > 0.5) provided correction with spectacles, if needed
- •Significant abnormalities related to important parts of the brain, e.g., the visual system, prefrontal cortex, or hippocampus, or relevant lesions detected by pre-trial imaging.
- •Prior history of significant diseases related to the visual system or the brain.
- •Medication: Use of any antiepileptic drugs, neuromodulating drugs or high dose of sedatives will be excluded.
- •Prior history of substance abuse within the past 2 years.
- •Any significant systemic illness or unstable medical condition, which could lead to difficulty complying with the protocol (at the discretion of the PI)
结局指标
主要结局
Gamma oscillations assessment
时间窗: Change from Baseline to 6 months and 7.5 months
Determine the total gamma power at 40 Hz, with no concomitant LTS device stimulation, assess changes in the gamma power at 40 Hz.
Induction of 40 Hz Gamma oscillations
时间窗: Change from Baseline to 6 months and 7.5 months
Estimate the change in electrical field patterns by EEG SSVEP, assess the difference between placebo and treatment for power spectral density signal to noise ratio at baseline measured by EEG SSVEP
次要结局
- Connectivity measures(Change from Baseline to 6 months and 7.5 months)
- MR Spectroscopy(Change from Baseline to 6 months and 7.5 months)
- MRI perfusion assessment(Change from Baseline to 6 months and 7.5 months)
- Safety Assessment(9 months)
- Cognition and memory assessment(Change from Baseline to 6 months and 7.5 months)
- Compliance assessment(Baseline to 6 months)
- Biomarkers of Alzheimer's Disease(Change from Baseline to 6 months and 7.5 months)
- Feasibility assessment(Baseline to 6 months)
- Sleep Quality(Change from Baseline to 6 months and 7.5 months)
- MRI Atrophy assessment(Change from Baseline to 6 months and 7.5 months)
- EEG: Spectral feature assessment(Change from Baseline to 6 months and 7.5 months)