Digital AVATAR therapy for distressing voices in psychosis: the phase 2/3 AVATAR2 trial

IF 58.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Philippa A. Garety, Clementine J. Edwards, Hassan Jafari, Richard Emsley, Mark Huckvale, Mar Rus-Calafell, Miriam Fornells-Ambrojo, Andrew Gumley, Gillian Haddock, Sandra Bucci, Hamish J. McLeod, Jeffrey McDonnell, Moya Clancy, Michael Fitzsimmons, Hannah Ball, Alice Montague, Nikos Xanidis, Amy Hardy, Thomas K. J. Craig, Thomas Ward
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Abstract

Distressing voices are a core symptom of psychosis, for which existing treatments are currently suboptimal; as such, new effective treatments for distressing voices are needed. AVATAR therapy involves voice-hearers engaging in a series of facilitated dialogues with a digital embodiment of the distressing voice. This randomized phase 2/3 trial assesses the efficacy of two forms of AVATAR therapy, AVATAR-Brief (AV-BRF) and AVATAR-Extended (AV-EXT), both combined with treatment as usual (TAU) compared to TAU alone, and conducted an intention-to-treat analysis. We recruited 345 participants with psychosis; data were available for 300 participants (86.9%) at 16 weeks and 298 (86.4%) at 28 weeks. The primary outcome was voice-related distress at both time points, while voice severity and voice frequency were key secondary outcomes. Voice-related distress improved, compared with TAU, in both forms at 16 weeks but not at 28 weeks. Distress at 16 weeks was as follows: AV-BRF, effect −1.05 points, 96.5% confidence interval (CI) = −2.110 to 0, P = 0.035, Cohen’s d = 0.38 (CI = 0 to 0.767); AV-EXT −1.60 points, 96.5% CI = −3.133 to −0.058, P = 0.029, Cohen’s d = 0.58 (CI = 0.021 to 1.139). Distress at 28 weeks was: AV-BRF, −0.62 points, 96.5% CI = −1.912 to 0.679, P = 0.316, Cohen’s d = 0.22 (CI = −0.247 to 0.695); AV-EXT −1.06 points, 96.5% CI = −2.700 to 0.586, P = 0.175, Cohen’s d = 0.38 (CI = −0.213 to 0.981). Voice severity improved in both forms, compared with TAU, at 16 weeks but not at 28 weeks whereas frequency was reduced in AV-EXT but not in AV-BRF at both time points. There were no related serious adverse events. These findings provide partial support for our primary hypotheses. AV-EXT met our threshold for a clinically significant change, suggesting that future work should be primarily guided by this protocol. ISRCTN registration: ISRCTN55682735.

Abstract Image

数字 AVATAR 疗法治疗精神病患者的痛苦声音:第 2/3 期 AVATAR2 试验
恼人的声音是精神病的一种核心症状,目前现有的治疗方法并不理想,因此需要针对恼人声音的新的有效治疗方法。AVATAR 疗法是让声音聆听者与困扰声音的数字化身进行一系列协助对话。这项随机2/3阶段试验评估了两种形式的AVATAR疗法(AVATAR-Brief(AV-BRF)和AVATAR-Extended(AV-EXT))的疗效,两种疗法均与常规治疗(TAU)相结合,与单独使用TAU相比,并进行了意向治疗分析。我们招募了 345 名精神病患者,其中 300 人(86.9%)在 16 周时有数据,298 人(86.4%)在 28 周时有数据。两个时间点的主要结果都是与嗓音相关的痛苦,而嗓音严重程度和嗓音频率则是主要的次要结果。与 TAU 相比,两种形式的嗓音相关困扰在 16 周时都有所改善,但在 28 周时没有改善。16 周时的嗓音困扰情况如下AV-BRF,影响-1.05点,96.5%置信区间(CI)=-2.110至0,P=0.035,Cohen's d=0.38(CI=0至0.767);AV-EXT-1.60点,96.5%置信区间(CI)=-3.133至-0.058,P=0.029,Cohen's d=0.58(CI=0.021至1.139)。28 周时的痛苦程度为AV-BRF -0.62分,96.5% CI = -1.912 至 0.679,P = 0.316,Cohen's d = 0.22(CI = -0.247 至 0.695);AV-EXT -1.06分,96.5% CI = -2.700 至 0.586,P = 0.175,Cohen's d = 0.38(CI = -0.213 至 0.981)。与TAU相比,两种形式的嗓音严重程度在16周时都有所改善,但在28周时没有改善,而频率在AV-EXT中都有所降低,但在AV-BRF中没有降低。没有发生相关的严重不良事件。这些研究结果为我们的主要假设提供了部分支持。AV-EXT 达到了我们的临床显著变化阈值,这表明未来的工作应主要以该方案为指导。ISRCTN 注册:ISRCTN55682735。
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来源期刊
Nature Medicine
Nature Medicine 医学-生化与分子生物学
CiteScore
100.90
自引率
0.70%
发文量
525
审稿时长
1 months
期刊介绍: Nature Medicine is a monthly journal publishing original peer-reviewed research in all areas of medicine. The publication focuses on originality, timeliness, interdisciplinary interest, and the impact on improving human health. In addition to research articles, Nature Medicine also publishes commissioned content such as News, Reviews, and Perspectives. This content aims to provide context for the latest advances in translational and clinical research, reaching a wide audience of M.D. and Ph.D. readers. All editorial decisions for the journal are made by a team of full-time professional editors. Nature Medicine consider all types of clinical research, including: -Case-reports and small case series -Clinical trials, whether phase 1, 2, 3 or 4 -Observational studies -Meta-analyses -Biomarker studies -Public and global health studies Nature Medicine is also committed to facilitating communication between translational and clinical researchers. As such, we consider “hybrid” studies with preclinical and translational findings reported alongside data from clinical studies.
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