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Working Memory Training in Alcohol Use Disorder: A Randomized Controlled Trial

BACKGROUND: Alcohol use disorder (AUD) is associated with cognitive deficits such as impaired executive functions, which are hypothesized to contribute to the progression of the disease and worsen treatment outcome. Training of working memory (WM) to improve cognitive functions and thereby reduce al...

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Autores principales: Khemiri, Lotfi, Brynte, Christoffer, Stunkel, Angela, Klingberg, Torkel, Jayaram‐Lindström, Nitya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587824/
https://www.ncbi.nlm.nih.gov/pubmed/30462837
http://dx.doi.org/10.1111/acer.13910
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author Khemiri, Lotfi
Brynte, Christoffer
Stunkel, Angela
Klingberg, Torkel
Jayaram‐Lindström, Nitya
author_facet Khemiri, Lotfi
Brynte, Christoffer
Stunkel, Angela
Klingberg, Torkel
Jayaram‐Lindström, Nitya
author_sort Khemiri, Lotfi
collection PubMed
description BACKGROUND: Alcohol use disorder (AUD) is associated with cognitive deficits such as impaired executive functions, which are hypothesized to contribute to the progression of the disease and worsen treatment outcome. Training of working memory (WM) to improve cognitive functions and thereby reduce alcohol use has been proposed as a novel treatment strategy. METHODS: Patients with AUD (n = 50) who were recruited to an outpatient addiction clinic were randomized to receive 5 weeks of active WM training or control training. Participants had weekly follow‐up visits, and all cognitive training sessions were done online at home. Primary outcomes were WM function and change in self‐reported heavy drinking. Secondary outcomes were craving, other drinking outcomes, and performance on a range of neuropsychological tasks from the Cambridge Neuropsychological Test Automated Battery. RESULTS: The active training group demonstrated a significantly greater improvement in verbal WM compared with the control group. No statistically significant effect of training was found on the primary drinking outcome, but a trend was observed indicating that WM training reduces the number of drinks per drinking occasion. WM training had no statistically significant effect on any of the other neuropsychological tasks. CONCLUSIONS: Cognitive training can improve WM function in individuals with AUD, suggesting that such interventions are feasible to administer in this patient population. The results do not support an effect of WM training on heavy drinking or transfer effects to other cognitive domains. Future studies should evaluate WM training as an adjunct to evidence‐based treatments for AUD to assess potential synergistic effects.
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spelling pubmed-65878242019-07-02 Working Memory Training in Alcohol Use Disorder: A Randomized Controlled Trial Khemiri, Lotfi Brynte, Christoffer Stunkel, Angela Klingberg, Torkel Jayaram‐Lindström, Nitya Alcohol Clin Exp Res Behavior, Treatment, and Prevention BACKGROUND: Alcohol use disorder (AUD) is associated with cognitive deficits such as impaired executive functions, which are hypothesized to contribute to the progression of the disease and worsen treatment outcome. Training of working memory (WM) to improve cognitive functions and thereby reduce alcohol use has been proposed as a novel treatment strategy. METHODS: Patients with AUD (n = 50) who were recruited to an outpatient addiction clinic were randomized to receive 5 weeks of active WM training or control training. Participants had weekly follow‐up visits, and all cognitive training sessions were done online at home. Primary outcomes were WM function and change in self‐reported heavy drinking. Secondary outcomes were craving, other drinking outcomes, and performance on a range of neuropsychological tasks from the Cambridge Neuropsychological Test Automated Battery. RESULTS: The active training group demonstrated a significantly greater improvement in verbal WM compared with the control group. No statistically significant effect of training was found on the primary drinking outcome, but a trend was observed indicating that WM training reduces the number of drinks per drinking occasion. WM training had no statistically significant effect on any of the other neuropsychological tasks. CONCLUSIONS: Cognitive training can improve WM function in individuals with AUD, suggesting that such interventions are feasible to administer in this patient population. The results do not support an effect of WM training on heavy drinking or transfer effects to other cognitive domains. Future studies should evaluate WM training as an adjunct to evidence‐based treatments for AUD to assess potential synergistic effects. John Wiley and Sons Inc. 2018-11-21 2019-01 /pmc/articles/PMC6587824/ /pubmed/30462837 http://dx.doi.org/10.1111/acer.13910 Text en © 2018 The Authors. Alcoholism: Clinical & Experimental Research published by Wiley Periodicals, Inc. on behalf of Research Society on Alcoholism This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Behavior, Treatment, and Prevention
Khemiri, Lotfi
Brynte, Christoffer
Stunkel, Angela
Klingberg, Torkel
Jayaram‐Lindström, Nitya
Working Memory Training in Alcohol Use Disorder: A Randomized Controlled Trial
title Working Memory Training in Alcohol Use Disorder: A Randomized Controlled Trial
title_full Working Memory Training in Alcohol Use Disorder: A Randomized Controlled Trial
title_fullStr Working Memory Training in Alcohol Use Disorder: A Randomized Controlled Trial
title_full_unstemmed Working Memory Training in Alcohol Use Disorder: A Randomized Controlled Trial
title_short Working Memory Training in Alcohol Use Disorder: A Randomized Controlled Trial
title_sort working memory training in alcohol use disorder: a randomized controlled trial
topic Behavior, Treatment, and Prevention
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587824/
https://www.ncbi.nlm.nih.gov/pubmed/30462837
http://dx.doi.org/10.1111/acer.13910
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