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Randomized Controlled Trial
. 2024 Dec;50(2):472-479.
doi: 10.1038/s41386-024-01995-z. Epub 2024 Oct 2.

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

Affiliations
Randomized Controlled Trial

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

Lindsay W Victoria et al. Neuropsychopharmacology. 2024 Dec.

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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Conflict of interest statement

Competing interests: LWV, LEO, AJ, RHP, and FMG reported receiving grants from the National Institute of Mental Health during the conduct of the study outside of the submitted work. In addition to receiving funding for the reported RCT, FG reported receiving a one-time consultant fee from Akili Interactive that was not directly related to the presented work. AJ consults for Axem Neurotechnologies Inc. and reported receiving fees and stock options outside the submitted work. CM, CAS, DNF, and SHK were employees of Akili Interactive and have owned stock or equity in the company. RHP reported receiving personal fees from the Burrage Capital Investment Fund, Genomind Genomics, Circular Genomics, and Takeda Preclinical scientific advising outside the submitted work. No other disclosures were reported.

References

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