联合促进:通过结合氯胺酮和神经反馈辅助学习来促进和指导神经可塑性——对可卡因成瘾的个体化和综合药物心理治疗:一项随机、安慰剂对照、双盲、平行组、单中心试验的研究方案。

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2025-09-25 DOI:10.1186/s13063-025-08982-9
Anna S Trippel, Ladina P Gubser, Etna J E Engeli, Jan Conradi, Amelie Haugg, Niklaus Zoelch, Marcus Herdener
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引用次数: 0

摘要

背景:可卡因是世界上最常用的兴奋剂,在欧洲的消费率越来越高。可卡因的使用对个人和社会都有极大的危害。到目前为止,对可卡因使用障碍(CUD)的心理治疗干预仅显示出适度的效果,由于对该疾病的了解存在空白,尚未批准任何药物治疗。然而,一种新的药物治疗靶点,即谷氨酸能神经传递,从成瘾的动物模型中出现。具体来说,在长期服用可卡因后,啮齿动物伏隔核(NAcc)中的谷氨酸浓度降低,而在线索诱导的可卡因寻找过程中,谷氨酸会溢出。最近,在CUD患者中也观察到这种谷氨酸能失衡。此外,关于新的心理治疗方法的有希望的发现来自神经反馈训练(NFT)研究,参与者使用认知策略来调节他们在特定大脑区域内的活动,基于实时功能磁共振成像(rt-fMRI)评估的“实时”反馈。例如,患有CUD的参与者成功地学会了使用奖励意象来调节他们在中脑奖励区域的大脑活动,并重新构建对非药物相关强化物的奖励敏感性,例如社会互动,运动或专业成就。因此,我们研究了两种干预措施的治疗潜力和潜在机制,单剂量氯胺酮和奖励成像rt-fMRI NFT对120名CUD参与者的治疗潜力和潜在机制。方法:我们研究了120名CUD患者的单次氯胺酮输注、三次奖励意象rt-fMRI NFT,以及与安慰剂输注或假NFT相比较的这些干预措施的组合。该研究采用随机、安慰剂对照、双盲的方式设计,共有四个研究组。讨论:我们期望这两种干预措施对可卡因使用天数的比例产生积极影响。我们预测奖励系统中的谷氨酸水平会随着氯胺酮输注而增加,并减少渴望,rt-fMRI NFT导致对自然奖励的敏感性再次增强,以及联合干预的协同效应。这种神经生物学信息的方法有可能通过个体化和综合药物-心理治疗为CUD的治疗开辟新的途径。试验注册:NCT06125054 ClinicalTrials.gov。注册于2023年10月26日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-Boost: boosting and guiding neuroplasticity by combining ketamine with neurofeedback-assisted learning-towards an individualised and integrated pharmaco-psychotherapy for cocaine addiction: study protocol for a randomised, placebo-controlled, double-blind, parallel-group, single-centre trial.

Background: Cocaine is the most frequently used stimulant worldwide, with increasing consumption rates in Europe. Cocaine use is associated with great harm to individuals and society. As of today, psychotherapeutic interventions for cocaine use disorder (CUD) demonstrate only modest effect sizes, and no pharmacotherapy has been approved due to gaps in understanding the disease. However, a novel pharmacotherapeutic target, i.e. glutamatergic neurotransmission, emerged from animal models of addiction. Specifically, after chronic cocaine administration, glutamate concentrations in the nucleus accumbens (NAcc) of rodents are reduced, while there is an overflow of glutamate during cue-induced cocaine-seeking. Recently, this glutamatergic imbalance has also been observed in humans with CUD. Additionally, promising findings with regard to novel psychotherapeutic approaches came from neurofeedback training (NFT) studies where participants use cognitive strategies to regulate their activity within a specific brain region based on "real-time" feedback about its activity as assessed by real-time functional magnetic resonance imaging (rt-fMRI). For example, participants with CUD successfully learned to regulate their brain activity in reward areas of the midbrain using reward imagery and to reconstitute reward sensitivity to non-drug related reinforcers like, e.g. social interactions, athletic or professional achievements. We therefore investigate the therapeutic potential and the underlying mechanisms of two interventions, a single dose of ketamine and a reward imagery rt-fMRI NFT in 120 participants with CUD.

Methods: We examine a single ketamine infusion, three sessions of reward imagery rt-fMRI NFT, and the combination of those interventions contrasted to a placebo infusion or a sham NFT in 120 participants with CUD. The study is designed in a randomized, placebo-controlled, double-blind fashion with four study arms.

Discussion: We expect both interventions to have a positive effect on the proportion of cocaine use days. We predict glutamate levels in the reward system to increase with the ketamine infusion and to reduce craving, a re-enhanced sensitivity towards natural rewards resulting from the rt-fMRI NFT, and synergistic effects of the combined interventions. This neurobiologically informed approach has the potential to open new avenues for the treatment of CUD through individualised and integrated pharmaco-psychotherapy.

Trial registration: NCT06125054 ClinicalTrials.gov. Registered on October 26, 2023.

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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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