跳至主要内容
临床试验/JPRN-jRCT1030230105
JPRN-jRCT1030230105招募中1 期

A comparative study of melanopsin-mediated pupillary responses among diseases with concomitant circadian rhythm sleep/wake disorders

Kitamura Shingo0 个研究点目标入组 100 人开始时间: 2023年6月2日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 16age old 至 <= 80age old(—)
性别
All

入选标准

  • DSWPD patients: 1) Participants who are between 16 and 29 years old at the time of consent. 2) Participants who meet DSM-5 or ICSD-3 diagnostic criteria for DSWPD
  • Healthy controls of DSWPD patients: 1) Participants who are between 16 and 29 years old at the time of consent.
  • AD Spectrum Patients: 1) Participants who are between 60 and 80 years old at the time of consent. 2) Participants who meet the diagnostic criteria for AD Spectrum (Mild AD, MCI, Preclinical AD) 3) Participants who fully understand the study and give their free and voluntary written consent.
  • Healthy controls of AD spectrum patients: 1) Participants who are between 60 and 80 years old at the time of consent. 2) Participants who fully understand the study and give their free and voluntary written consent

排除标准

  • DSWPD patients: 1) Participants with neurodegenerative diseases. 2) Participants with abnormal color vision. 3) Participants with darkness phobia. 4) Other subjects deemed inappropriate by the principal investigator.
  • Healthy controls of DSWPD: 1) Participants with psychiatric disorders. 2) Participants with neurodegenerative disorders. 3) Participants with abnormal color vision. 4) Participants with darkness phobia. 5) Other subjects deemed inappropriate by the principal investigator.
  • AD Spectrum Patients: 1) Participants with neurodegenerative diseases other than AD Spectrum. 2) Participants with abnormal color vision. 3) Those with darkness phobia. 4) Others whom the principal investigator deems inappropriate.
  • Healthy controls of AD spectrum: 1) Participants with psychiatric disorders. 2) Participants with neurodegenerative disorders. 3) Participants with abnormal color vision. 4) Participants with darkneess phobia. 5) Other subjects deemed inappropriate by the principal investigator.

研究者

发起方
Kitamura Shingo

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