Center for Research on End-of-Life Care, Weill Cornell Medicine, New York, NY, USA.
Department of Psychiatry, Weill Cornell Medicine, New York, NY, USA.
Trials. 2021 Feb 1;22(1):110. doi: 10.1186/s13063-021-05044-8.
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.
METHODS/DESIGN: 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.
目前针对延长哀伤障碍(PGD)尚无有效的药物治疗方法。有证据表明,PGD 的神经生物学涉及与奖励通路相同的回路。基于这一证据,我们假设 PGD 可以被视为一种成瘾障碍,因此可以从目前用于治疗此类障碍的药物中获益。其中一种药物是纳曲酮,它目前用于治疗酒精和阿片类药物依赖。选择口服纳曲酮是基于其作用机制、安全性和便利性。本研究的主要目的是确定口服纳曲酮作为 PGD 药物治疗的疗效。具体来说,我们假设与安慰剂相比,接受纳曲酮治疗的参与者的 PGD 症状会减轻。
方法/设计:这是一项随机、安慰剂对照、三盲(对医护人员/研究人员、参与者和数据分析师)研究,我们计划招募符合延长哀伤障碍(PGD)标准的 48 名参与者。参与者将被随机分配到纳曲酮 50mg 口服组或安慰剂组;药物将被过度封装,使其看起来完全相同。参与者将服用指定的药物 8 周,每 4 周进行一次就诊,以评估症状严重程度、社交亲密程度和不良反应。每周使用修订后的延长哀伤 13 项量表(PG-13-R)调查将纳曲酮的使用与 PGD 症状严重程度的变化联系起来。最后一次就诊后 4 周进行随访,评估治疗的持久性以及任何持续的不良反应。
这项研究是首次探索口服纳曲酮作为 PGD 药物治疗的用途。该疾病的急性和衰弱性质,加上共病风险增加,突出了对纳曲酮等药物治疗的需求,这种治疗方法起效更快,可以帮助那些心理治疗可能无效的患者,和/或可以增强心理治疗以促进 PGD 症状的缓解。
ClinicalTrials.gov NCT04547985。注册于 2020 年 8 月 31 日。