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Naltrexone treatment for prolonged grief disorder: study protocol for a randomized, triple-blinded, placebo-controlled trial

机译:纳曲酮治疗长期悲伤障碍:用于随机,三重盲,安慰剂对照试验的研究方案

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There is a lack of effective pharmacotherapy for prolonged grief disorder (PGD). Evidence suggests that the neurobiology of PGD involves the same circuitry as the reward pathway. Based upon this evidence, we hypothesize that PGD can be conceptualized as a disorder of addiction and therefore could benefit from being treated with medications that are currently used to treat such disorders. One such medication is naltrexone, which is currently used to treat alcohol and opioid dependence. Oral naltrexone was chosen for its mechanism of action, safety, and convenience. The primary aim of this study is to establish the efficacy of using oral naltrexone as a pharmacological treatment for PGD. Specifically, we hypothesize that participants receiving naltrexone will demonstrate reduced PGD symptoms when compared to placebo. This is a randomized, placebo-controlled, triple-blinded (to healthcare professionals/study staff, participants, and data analysts) study in which we propose to enroll 48 participants who meet criteria for Prolonged Grief Disorder (PGD). Participants will be randomly assigned to the naltrexone 50?mg oral arm or placebo arm; medications will be over-encapsulated to appear identical. Participants will take their assigned medication for 8?weeks, with clinic visits every 4?weeks to assess symptom severity, social closeness, and adverse reactions. Weekly surveys of Prolonged Grief-13-Revised (PG-13-R) will be used to relate naltrexone use to changes in PGD symptom severity. Follow-up 4?weeks after their last visit will assess the longevity of treatment, as well as any lingering adverse reactions. This study is the first to investigate the use of oral naltrexone as pharmacological treatment for PGD. The acute and debilitating nature of the disorder, in addition to the increased risk of comorbidities, highlights the need for pharmacological treatment like naltrexone that can act more rapidly, may help those for whom psychotherapy may not be effective, and/or may augment psychotherapy to promote PGD symptom grief resolution. ClinicalTrials.gov NCT04547985 . Registered on 8/31/2020.
机译:延长悲伤障碍(PGD)缺乏有效的药物疗法。证据表明PGD的神经生物学涉及与奖励途径相同的电路。基于这种证据,我们假设PGD可以概念化为成瘾障碍,因此可以从目前用于治疗此类疾病的药物治疗。一种这样的药物是纳曲酮,目前用于治疗醇和阿片类药物的依赖。口服纳曲酮被选为其作用,安全和便利机制。本研究的主要目的是建立使用口服纳曲酮作为PGD的药理学治疗的疗效。具体而言,我们假设接受纳曲酮的参与者将在与安慰剂相比时证明PGD症状减少。这是一项随机,安慰剂控制的三重蒙蔽(对医疗保健专业人员/学习人员,参与者和数据分析师)研究,我们建议注册48名参与者达到长期悲伤障碍(PGD)的标准。参与者将随机分配给纳曲线50?Mg口腔臂或安慰剂臂;药物将过度封装出现相同。参与者将持有8个?几周的药物治疗,诊所每4个星期进行一次评估症状严重程度,社会闭合和不良反应。每周调查长期悲伤-13修订(PG-13-R)将用于涉及纳曲酮用于改变PGD症状严重程度。随访4?上次访问后几周将评估治疗的寿命,以及任何挥之不去的不良反应。本研究是第一个调查使用口腔纳曲酮作为PGD药理治疗的使用。症状的急性和衰弱性质,除了具有较快的纳曲酮等丙酮酮等药物治疗外,急性和衰弱性的性质还突出可迅速行动,可以帮助那些心理治疗可能没有有效的人,和/或增加心理治疗促进PGD症状悲伤决议。 ClinicalTrials.gov NCT04547985。注册于8/31/2020。

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