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Acute Mood-Elevating Properties of Microdosed Lysergic Acid Diethylamide in Healthy Volunteers: A Home-Administered Randomized Controlled Trial

机译:微剂量麦角酸二乙酰胺在健康志愿者中的急性情绪提升特性:一项家庭管理的随机对照试验

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? 2023 Society of Biological PsychiatryBackground: Microdosing psychedelic drugs is a widespread social phenomenon with diverse benefits claimed for mood and cognition. Randomized controlled trials have failed to support these claims, but the laboratory-based dosing in trials conducted to date may have limited ecological validity. Methods: Healthy male volunteers were randomized into lysergic acid diethylamide (LSD) (n = 40) and placebo (n = 40) groups and received 14 doses of either 10 μg LSD or an inactive placebo every 3 days for 6 weeks. First doses were given in a supervised laboratory setting, with other doses self-administered in a naturalistic setting. Results of safety data, blinding, daily questionnaires, expectancy, and pre-/postintervention psychometrics and cognitive tasks are presented here. Results: The most notable reported adverse event was treatment-related anxiety, which prompted the withdrawal of 4 participants from the LSD group. Daily questionnaires showed credible evidence (>99 posterior probability) of improved ratings of creativity, connectedness, energy, happiness, irritability, and wellness on dose days compared with nondose days, and these effects remained when controlling for preintervention expectancy. No questionnaire or cognitive task showed a credible change between baseline and 6-week assessment time points. Conclusions: Microdosing LSD appears to be relatively safe in healthy adult men, notwithstanding a risk of anxiety. While microdosing elicited transient increases in scales associated with mood-elevating effects, it was not sufficient to promote enduring changes to overall mood or cognition in healthy adults. Future microdosing trials in clinical populations will require the use of active placebos to control for placebo effects and dose titration to adjust for interindividual variability in drug response.
机译:?2023 生物精神病学学会背景:微剂量迷幻药是一种普遍的社会现象,对情绪和认知有多种益处。随机对照试验未能支持这些说法,但迄今为止进行的试验中基于实验室的剂量可能具有有限的生态有效性。方法:健康男性志愿者被随机分为麦角酸二乙酰胺 (LSD) (n = 40) 和安慰剂 (n = 40) 组,每 3 天接受 14 剂 10 μg LSD 或非活性安慰剂,持续 6 周。第一剂在受监督的实验室环境中给药,其他剂量在自然环境中自行给药。这里介绍了安全数据、盲法、每日问卷调查、期望以及干预前/干预后心理测量和认知任务的结果。结果:最显着的不良事件是与治疗相关的焦虑,这促使 4 名参与者退出 LSD 组。每日问卷调查显示,与非给药日相比,剂量日对创造力、连通性、能量、幸福感、易怒和健康的评分有所提高(>99% 后验概率),并且在控制干预前预期时,这些影响仍然存在。没有问卷或认知任务显示基线和 6 周评估时间点之间有可信的变化。结论:微剂量LSD在健康成年男性中似乎相对安全,尽管存在焦虑的风险。虽然微剂量会引起与情绪提升效应相关的量表的短暂增加,但不足以促进健康成年人整体情绪或认知的持久变化。未来在临床人群中进行的微剂量试验将需要使用活性安慰剂来控制安慰剂效应,并使用剂量滴定来调整药物反应的个体间差异。

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