A digital intervention for cognitive deficits following COVID-19: a randomized clinical trial.

IF 6.6 1区 医学 Q1 NEUROSCIENCES Neuropsychopharmacology Pub Date : 2024-10-02 DOI:10.1038/s41386-024-01995-z
Lindsay W Victoria, Lauren E Oberlin, Irena P Ilieva, Abhishek Jaywant, Dora Kanellopoulos, Catherine Mercaldi, Caitlin A Stamatis, Deborah N Farlow, Scott H Kollins, Ochuwa Tisor, Sama Joshi, Raura Doreste-Mendez, Roy H Perlis, Faith M Gunning
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Abstract

Post-COVID-19 cognitive deficits are common, persistent, and disabling. Evidence on effective treatments is limited. The goal of this study was to investigate the efficacy of a digital intervention to reduce cognitive and functional deficits in adults with persistent post-COVID-19 cognitive dysfunction. We used the remotely-delivered intervention in a randomized clinical trial conducted from July 13, 2021 to April 26, 2023. We hypothesized that participants in the intervention group would improve in measures of cognition and daily functioning. Participants were adults with cognitive deficits persisting >4 weeks following acute COVID-19 illness. Of 183 participants screened, 110 were enrolled; 98 participants (78.6% female; mean age = 48.1) completed at least one study visit. Participants were randomized 1:1 to the intervention (AKL-T01) or waitlist control. AKL-T01 is a digital therapeutic using a videogame interface to target attention and executive control. The intervention was delivered remotely for 6 weeks. The primary outcome was change in performance on a sustained attention measure (Digit Symbol Matching Task). The difference in the primary outcome between the intervention (n = 49) and controls (n = 49) was not statistically significant (F [3,261] = 0.12, p = 0.95). Secondary cognitive outcomes of task-switching (F[3,262] = 2.78, p = 0.04) and processing speed (F[3,267] = 4.57, p = 0.004) improved in the intervention relative to control. Secondary measures of functioning also improved in the intervention relative to control, including disability (F[1,82] = 4.02, p = 0.05) and quality of life (F[3,271] = 2.66, p = 0.05). Exploratory analyses showed a greater reduction in total fatigue (F[1,85] = 4.51, p = 0.04), cognitive fatigue (F[1,85] = 7.20, p = 0.009), and anxiety (F[1,87] = 7.42, p = 0.008) in the intervention relative to control. Despite the lack of improvement in sustained attention, select post-COVID-19 cognitive deficits may be ameliorated by targeted cognitive training with AKL-T01, with associated improvements in quality of life and fatigue. If replicated, the scalable nature of this digital intervention may help address substantial need for accessible, effective treatments among individuals with long COVID.

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针对 COVID-19 后认知障碍的数字干预:随机临床试验。
COVID-19 后认知障碍是一种常见的、持续性和致残性障碍。有效治疗的证据有限。本研究的目的是调查一种数字干预方法对减少 COVID-19 后持续性认知功能障碍成人的认知和功能障碍的疗效。我们在 2021 年 7 月 13 日至 2023 年 4 月 26 日进行的随机临床试验中使用了远程交付的干预方法。我们假设干预组的参与者在认知和日常功能方面会有所改善。参与者是在急性 COVID-19 疾病后认知障碍持续超过 4 周的成年人。在经过筛选的 183 名参与者中,有 110 人被纳入干预组;98 人(78.6% 为女性;平均年龄为 48.1 岁)至少完成了一次研究访问。参与者按 1:1 随机分配到干预(AKL-T01)或候补对照组。AKL-T01 是一种使用电子游戏界面的数字疗法,以注意力和执行控制为目标。干预措施通过远程方式进行,为期 6 周。主要结果是持续注意力测量(数字符号匹配任务)成绩的变化。干预组(49 人)与对照组(49 人)的主要结果差异无统计学意义(F [3,261] = 0.12,P = 0.95)。与对照组相比,干预组的任务转换(F[3,262] = 2.78,p = 0.04)和处理速度(F[3,267] = 4.57,p = 0.004)等次要认知结果有所改善。与对照组相比,干预组的次要功能指标也有所改善,包括残疾(F[1,82] = 4.02,p = 0.05)和生活质量(F[3,271] = 2.66,p = 0.05)。探索性分析表明,与对照组相比,干预组的总体疲劳(F[1,85] = 4.51,p = 0.04)、认知疲劳(F[1,85] = 7.20,p = 0.009)和焦虑(F[1,87] = 7.42,p = 0.008)减少幅度更大。尽管在持续注意力方面没有改善,但通过使用 AKL-T01 进行有针对性的认知训练,COVID-19 后的某些认知缺陷可能会得到改善,生活质量和疲劳也会随之改善。如果能够得到推广,这种数字干预的可扩展性将有助于满足长期 COVID 患者对可获得的有效治疗方法的大量需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuropsychopharmacology
Neuropsychopharmacology 医学-精神病学
CiteScore
15.00
自引率
2.60%
发文量
240
审稿时长
2 months
期刊介绍: Neuropsychopharmacology is a reputable international scientific journal that serves as the official publication of the American College of Neuropsychopharmacology (ACNP). The journal's primary focus is on research that enhances our knowledge of the brain and behavior, with a particular emphasis on the molecular, cellular, physiological, and psychological aspects of substances that affect the central nervous system (CNS). It also aims to identify new molecular targets for the development of future drugs. The journal prioritizes original research reports, but it also welcomes mini-reviews and perspectives, which are often solicited by the editorial office. These types of articles provide valuable insights and syntheses of current research trends and future directions in the field of neuroscience and pharmacology.
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