通过提高神经性厌食症患者的奖赏反应性减少复发:VIBRANT(神经性厌食症治疗后促进康复的虚拟干预)试验†。

Journal of psychiatry and brain science Pub Date : 2024-01-01 Epub Date: 2024-08-16 DOI:10.20900/jpbs.20240005
Ann F Haynos, Kira G Venables, Lisa M Anderson, Michelle G Craske, Carol B Peterson
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引用次数: 0

摘要

导言:神经性厌食症(AN)出院后的急性期是复发率较高的高危期,许多患者无法获得有效的治疗。即使在急性营养状况稳定后,厌食症的特点仍是对一般奖赏的生物行为敏感性降低,而对体重减轻线索的敏感性升高。这些奖赏模式可能会继续维持进食障碍和合并情感症状。为了填补急性厌食症后治疗文献中的这些空白,我们提出了一项随机对照试验,将针对急性厌食症后饮食失调的积极情绪治疗(PAT-AN)与更标准的心理教育和行为治疗(PBT)进行比较:方法:在过去6个月内从AN强化治疗(如住院治疗、部分住院治疗)中出院的患有广泛AN(包括非典型AN)的成人参与者(N = 80)将被随机分配到为期24周的远程PAT-AN或PBT治疗中。我们将比较每种治疗方法的可行性、可接受性和疗效,以增强急性自闭症急性期后门诊治疗的效果。多模态神经认知和自我报告电池将评估治疗过程中(即基线、治疗中期、治疗后、三个月随访)和每周的进食病理、合并症状和假定奖赏机制的变化:本试验将首次直接针对观察到的自闭症急性期后的奖赏障碍进行研究。因此,这项研究有可能同时评估一种新型、有效的AN治疗方法,并进一步评估奖赏功能障碍在AN维持过程中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reducing Relapse by Enhancing Reward Responsivity in Anorexia Nervosa: The VIBRANT (Virtual Interventions for Bolstering Recovery following Anorexia Nervosa Treatment) Trial .

Introduction: The post-acute phase of anorexia nervosa (AN) following discharge from higher-level care is a high-risk period in which relapse rates are high and many individuals lack access to effective treatment. Even after acute nutritional stabilization, AN is characterized by decreased biobehavioral sensitivity towards general rewards and elevated sensitivity towards weight-loss cues. These reward patterns may continue to maintain eating disorder and comorbid affective symptoms. To address these gaps in the treatment literature for post-acute AN, we propose a randomized controlled trial comparing Positive Affect Treatment for AN (PAT-AN), a neuroscience-informed therapy adapted to target these reward imbalances in AN, to more standard psychoeducational and behavioral treatment (PBT) for eating disorders following acute care.

Method: Adult participants (N = 80) with broad AN, including atypical AN, discharged from intensive treatment (e.g., residential, partial hospitalization) for AN within the past 6 months will be randomly assigned to 24 weeks of remotely-delivered PAT-AN or PBT. We will compare the feasibility, acceptability, and efficacy of each treatment to augment post-acute outpatient care for AN. A multimodal neurocognitive and self-report battery will assess eating pathology, comorbid symptom, and putative reward mechanism changes over the course of treatment (i.e., baseline, mid-treatment, post-treatment, three-month follow-up) and on a week-to-week basis.

Discussion: This trial will, for the first time, directly target observed reward disturbances in the post-acute period of AN. Thus, this investigation has the potential to simultaneously evaluate a novel, efficacious treatment for AN and to further evaluate the role of reward dysfunction in AN maintenance.

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