Forma Felicia, Pratiwadi Ramya, El-Moustaid Fadoua, Smith Nathaniel, Thorndike Frances, Velez Fulton
Pear Therapeutics (US), Inc, Boston, MA, USA.
Maple Health Group, LLC, New York, NY, USA.
Curr Med Res Opin. 2022 Oct;38(10):1727-1738. doi: 10.1080/03007995.2022.2108616. Epub 2022 Aug 23.
The purpose of this study was to compare the effectiveness of the only Food and Drug Administration-authorized prescription digital therapeutic (PDT) Somryst versus face-to-face cognitive behavioral therapy for insomnia (CBT-I), or FDA-approved prescription medications for insomnia.
A systematic literature review was undertaken to identify relevant studies. A Bayesian network meta-analysis (NMA) was conducted to examine (1) mean change in insomnia severity index (ISI); (2) proportional change in ISI remitters; (3) mean change in wake after sleep onset (WASO); and (4) mean change in sleep onset latency (SOL).
Twenty studies provided data on the PDT, CBT-I, CBT-I in combination with self-help (SH), or two prescription medications (eszopiclone and zolpidem). The PDT was associated with significant mean change in ISI (-5.77, 95% Credible Interval [CrI] - 8.53, -3.07) and ISI remitters (OR 12.33; 95% CrI 2.28, 155.91) compared to placebo, and had the highest probability of being the most effective treatment overall for ISI mean change (56%), and ISI remitters (64%). All evaluated interventions significantly outperformed placebo for WASO but no significant differences were observed for SOL (five interventions). Sensitivity analyses excluding medications and meta-regression (assessing type, duration, delivery method for CBT-I) did not affect NMA results.
This network meta-analysis demonstrated that a PDT delivering CBT-I had the highest probability of being most effective compared to face-to-face CBT-I, prescription sleep medications, or placebo, as measured by reductions in mean ISI score from baseline and ISI-determined remittance.
本研究旨在比较美国食品药品监督管理局(FDA)唯一授权的处方数字疗法(PDT)Somryst与面对面认知行为疗法治疗失眠(CBT-I)或FDA批准的失眠处方药物的疗效。
进行系统的文献综述以确定相关研究。进行贝叶斯网络荟萃分析(NMA)以检验:(1)失眠严重程度指数(ISI)的平均变化;(2)ISI缓解者的比例变化;(3)睡眠开始后觉醒(WASO)的平均变化;(4)睡眠开始潜伏期(SOL)的平均变化。
20项研究提供了关于PDT、CBT-I、CBT-I联合自助(SH)或两种处方药物(艾司佐匹克隆和唑吡坦)的数据。与安慰剂相比,PDT与ISI的显著平均变化(-5.77,95%可信区间[CrI] -8.53,-3.07)和ISI缓解者(OR 12.33;95% CrI 2.28,155.91)相关,并且在ISI平均变化(56%)和ISI缓解者(64%)方面总体上最有效的治疗概率最高。所有评估的干预措施在WASO方面均显著优于安慰剂,但在SOL方面未观察到显著差异(五项干预措施)。排除药物的敏感性分析和荟萃回归(评估CBT-I的类型、持续时间、实施方式)不影响NMA结果。
该网络荟萃分析表明,与面对面CBT-I、处方睡眠药物或安慰剂相比,提供CBT-I的PDT从基线平均ISI评分降低和ISI确定的缓解情况衡量,最有效的概率最高。