Study on the effect of 40 Hz non-invasive light therapy system. A protocol for a randomized, double-blinded, placebo-controlled clinical trial

被引:3
|
作者
Agger, Mikkel Pejstrup [1 ,2 ]
Horning, Maibritt [1 ,2 ]
Carstensen, Marcus Schultz [3 ]
Danielsen, Else Rubaek [4 ]
Baandrup, Anders Olhues [4 ]
Nguyen, Mai [5 ]
Hogh, Peter [1 ,2 ]
Miskowiak, Kamilla [6 ,7 ]
Petersen, Paul Michael [3 ]
Madsen, Kristoffer Hougaard [8 ]
Kjaer, Troels Wesenberg [1 ,2 ]
机构
[1] Zealand Univ Hosp, Dept Neurol, Roskilde, Denmark
[2] Univ Copenhagen, Fac Hlth & Med Sci, Dept Clin Med, Copenhagen, Denmark
[3] Tech Univ Denmark, Dept Elect & Photon Engn, Lyngby, Denmark
[4] Zealand Univ Hosp, Dept Radiol, Roskilde, Denmark
[5] OptoCeut ApS, Lyngby, Denmark
[6] Copenhagen Univ Hosp, Neurocognit & Emot Affect Disorders NEAD Ctr, Psychiat Ctr Copenhagen, Rigshosp, Blegdamsvej 9, DK-2100 Copenhagen, Denmark
[7] Univ Copenhagen, Fac Social Sci, Dept Psychol, Copenhagen, Denmark
[8] Tech Univ Denmark, Dept Appl Math & Comp Sci, Lyngby, Denmark
来源
关键词
Alzheimer's disease; gamma entrainment; 40; Hz; light-based neurostimulation; Invisible Spectral Flicker; ALZHEIMERS-DISEASE; STIMULATION; FLICKER;
D O I
10.3389/fnagi.2023.1250626
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Introduction With no cure or effective treatment, the prevalence of patients with Alzheimer's disease (AD) is expected to intensify, thereby increasing the social and financial burden on society. Light-based 40 Hz brain stimulation is considered a novel treatment strategy for patients with AD that may alleviate some of this burden. The clinical trial ALZLIGHT will utilize a novel Light Therapy System (LTS). The LTS uses Invisible Spectral Flicker for non-invasive induction of 40 Hz neural activity. This protocol describes a trial evaluating the efficacy and safety of a light-based 40 Hz brain stimulation in patients with mild-to-moderate AD.Methods 62 patients with mild-to-moderate AD will participate in a randomized, double-blinded, placebo-controlled, parallel-group, and single-center trial. The participants will partake in an enrollment period of 1 month, an intervention period of 6 months, and a 1.5-month post-interventional follow-up period. Prior to the baseline measurement (week 0), the patients will be randomized to either active or placebo intervention from baseline (week 0) to post-intervention follow-up (week 26).Discussion This protocol describes a randomized, double-blinded, placebo-controlled clinical trial that may increase the understanding of the effect of gamma oscillations in the human brain and how it could be utilized as a novel and important tool for the treatment of AD. The effect is measured through a large, multidisciplinary assessment battery. Clinical trial registration:www.ClinicalTrials.gov, (NCT05260177). Registered on March 2, 2022.Discussion This protocol describes a randomized, double-blinded, placebo-controlled clinical trial that may increase the understanding of the effect of gamma oscillations in the human brain and how it could be utilized as a novel and important tool for the treatment of AD. The effect is measured through a large, multidisciplinary assessment battery. Clinical trial registration:www.ClinicalTrials.gov, (NCT05260177). Registered on March 2, 2022.
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页数:9
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