Department of Psychological Medicine, Faculty of Medical and Health Sciences, University of Auckland, 22-30 Park Avenue, Grafton, Auckland, 1023, New Zealand.
Department of Psychological Medicine, Division of Health Sciences, University of Otago, 464 Cumberland Street, Central Dunedin, Dunedin, 9016, New Zealand.
Trials. 2024 May 21;25(1):336. doi: 10.1186/s13063-024-08174-x.
Symptoms of anxiety and depression are common in patients with terminal illness and multiple challenges exist with timely and effective care in this population. Several centres have reported that one dose of the serotonergic psychedelic psilocybin, combined with therapeutic support, improves these symptoms for up to 6 months in this patient group. Drawing upon related therapeutic mechanisms, 3,4-methylenedioxymethamphetamine (MDMA)-assisted therapy may have the potential to achieve similar, positive mental health outcomes in this group. Preliminary evidence also supports the tolerability of MDMA-assisted therapy for anxiety and depression in advanced-stage cancer.
Up to 32 participants with advanced-stage cancer and associated depression and anxiety will be randomised in a 1:1 ratio into one of two blinded parallel treatment arms. The intervention group will receive 120 mg (+ 60 mg optional supplemental dose) MDMA-assisted therapy. The psychoactive control group will receive 20 mg oral (+ 10 mg optional supplemental dose) methylphenidate-assisted therapy. For each medication-assisted therapy session, participants will undergo two 90-min therapeutic support sessions in the week preceding, and one 90-min support session the day after the experimental session. A battery of measures (mood, anxiety, quality of life, mystical experience, spiritual wellbeing, attitudes towards death, personality traits, holistic health and wellbeing, connectedness, demoralisation, expectations, qualitative data and safety measures) will be assessed at baseline and through to the end of the protocol. Participants will be followed up until either 12 months post-randomisation or death, whichever occurs first.
This study will examine the effect of MDMA-assisted therapy on symptoms of anxiety and depression in advanced-stage cancer. Potential therapeutic implications include establishing the safety and effectiveness of a novel treatment that may relieve mental suffering in patients with life-threatening illness.
Trial registered on Australian New Zealand Clinical Trials Registry.
ACTRN12619001334190p. Date registered: 30/09/2019. URL: https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=378153&showOriginal=true&isReview=true.
焦虑和抑郁症状在终末期疾病患者中很常见,但在这一人群中及时有效地进行治疗存在诸多挑战。有几个中心报告称,在这组患者中,单次使用血清素能致幻剂裸盖菇素,结合治疗支持,可将这些症状改善长达 6 个月。基于相关治疗机制,3,4-亚甲二氧基甲基苯丙胺(MDMA)辅助疗法有可能在这一组中取得类似的积极心理健康结果。初步证据也支持 MDMA 辅助疗法在晚期癌症患者中治疗焦虑和抑郁的耐受性。
最多 32 名患有晚期癌症并伴有抑郁和焦虑的参与者将以 1:1 的比例随机分为两个双盲平行治疗组之一。干预组将接受 120mg(+60mg 可选补充剂量)MDMA 辅助治疗。精神兴奋剂对照组将接受 20mg 口服(+10mg 可选补充剂量)哌甲酯辅助治疗。对于每个药物辅助治疗疗程,参与者将在实验疗程前一周进行两次 90 分钟的治疗支持疗程,以及在实验疗程后一天进行一次 90 分钟的支持疗程。一系列措施(情绪、焦虑、生活质量、神秘体验、精神幸福感、对死亡的态度、人格特质、整体健康和幸福感、联系、沮丧、期望、定性数据和安全措施)将在基线和协议结束时进行评估。参与者将被随访至随机分组后 12 个月或死亡,以先发生者为准。
本研究将检查 MDMA 辅助治疗对晚期癌症患者焦虑和抑郁症状的影响。潜在的治疗意义包括确定一种新疗法的安全性和有效性,该疗法可能缓解威胁生命的疾病患者的精神痛苦。
该试验在澳大利亚和新西兰临床试验注册中心注册。
ACTRN12619001334190p。注册日期:2019 年 9 月 30 日。网址:https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=378153&showOriginal=true&isReview=true。