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Determining the Efficacy of Electronic Cognitive Behavioral Therapy for Generalized Anxiety Disorder Compared to Pharmaceutical Interventions: Protocol for a Quasi-Experimental Study

机译:与药品干预相比,确定电子认知行为治疗对广义焦虑障碍的疗效:准实验研究的议定书

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Background Generalized anxiety disorder (GAD) is an extremely prevalent and debilitating mental health disorder. Currently, the gold standard treatment for GAD is cognitive behavioral therapy (CBT) and/or pharmacotherapy. The most common medications used to treat GAD are selective serotonin reuptake inhibitors and selective norepinephrine reuptake inhibitors. While CBT is the gold standard treatment for GAD, it is costly, time-consuming, and often inaccessible. Fortunately, the electronic delivery of CBT (e-CBT) has emerged as a promising solution to address these barriers. e-CBT has shown to offer comparable results to in-person CBT while improving accessibility for patients and time efficiency for clinicians. Objective This study aims to investigate the treatment efficacy of e-CBT compared to and in conjunction with pharmacotherapy for GAD. Methods This study will use a quasi-experimental design to allow patients the freedom to choose which treatment modality they would like to receive. Participants with a diagnosis of GAD will be enrolled in 1 of 3 possible treatment arms: (1) e-CBT, (2) medication, or (3) a combination of e-CBT and medication. The e-CBT program will include a 12-week psychotherapy program delivered through the Online Psychotherapy Tool—a secure, cloud-based, digital mental health platform. The treatment efficacy of e-CBT will be compared with that of medication alone and medication in combination with e-CBT. Results The study received ethics approval in April 2019 and participant recruitment began in June 2019. Participant recruitment has been conducted through social media advertisements, physical advertisements, and physician referrals. To date, 146 participants (e-CBT: n=53; medication: n=49; combination: n=44) have been recruited. Data collection is expected to conclude by June 2021, and data analysis is expected to be completed by October 2021. Linear regression (for continuous outcomes) and binomial regression (for categorical outcomes) analysis will be conducted using interpretive qualitative methods. Conclusions If either the efficacy of e-CBT is shown to be comparable to that of medication or the effects of both treatments are augmented when used in tandem, these findings could have major implications on the mental health care system. e-CBT is a more accessible and affordable treatment that could increase mental health care capacity 4-fold if proven viable.
机译:背景技术广泛性焦虑症(GAD)是一种极其普遍和令人衰弱的心理健康障碍。目前,GAD的黄金标准治疗是认知行为治疗(CBT)和/或药物治疗。用于治疗GAD的最常见的药物是选择性血清素再摄取抑制剂和选择性去甲肾上腺素再摄取抑制剂。虽然CBT是GAD的黄金标准治疗,但它昂贵,耗时,往往无法进入。幸运的是,CBT(E-CBT)的电子传递已成为解决这些障碍的有希望的解决方案。 E-CBT已显示对患者的患者和临床医生的时间效率提供可比的结果。目的本研究旨在探讨E-CBT与GAD的药物疗法相比的治疗疗效。方法本研究将使用准实验设计,让患者自由选择他们希望接收的治疗方式。参与剂的诊断剂将参加3种可能的治疗臂中的1个:(1)E-CBT,(2)药物,或(3)E-CBT和药物的组合。 E-CBT计划将包括通过在线心理治疗工具提供的12周心理治疗计划 - 以安全,云,数字心理健康平台提供。 E-CBT的治疗疗效将与单独的药物和药物与E-CBT联合的药物进行比较。结果研究进入2019年4月的伦理批准,2019年6月的参与者招聘。参与者招聘是通过社交媒体广告,物理广告和医生推荐进行的。迄今为止,146名参与者(E-CBT:n = 53;药物:n = 49;组合:n = 44)已经招募。预计数据收集将在6月2021年6月结束,预计数据分析将在10月2021年完成。利用解释性定性方法进行线性回归(对于连续结果)和二项式回归(用于分类结果)分析。结论如果E-CBT的功效显示与药物的疗效或两种治疗的效果相当,则在串联中使用时增强,这些结果可能对心理保健系统产生重大影响。 E-CBT是一种更可达且价格合理的治疗,如果证明可行,可以增加精神保健能力4折。

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