The combination of donepezil and cognitive training for improving treatment outcomes for alcohol use disorder: Design of a randomized controlled trial

被引:2
作者
Yoon, Gihyun [1 ,2 ]
Sofuoglu, Mehmet [1 ,2 ]
Petrakis, Ismene L. [1 ,2 ]
Pittman, Brian [2 ]
Bell, Morris D. [1 ,2 ]
机构
[1] VA Connecticut Healthcare Syst, West Haven, CT USA
[2] Yale Sch Med, Dept Psychiat, New Haven, CT USA
基金
美国国家卫生研究院;
关键词
Alcohol use disorder; Donepezil; Pharmacotherapy; Cognitive training; Clinical trial; PLACEBO-CONTROLLED TRIAL; SUBSTANCE USE; NEUROCOGNITIVE IMPAIRMENT; REMEDIATION THERAPY; WORKING-MEMORY; BINGE DRINKING; ADOLESCENCE; MEDICATIONS; DEPENDENCE; COMPONENT;
D O I
10.1016/j.cct.2024.107657
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: The development of alcohol use disorder (AUD) is a major concern in public health, and cognitive impairments caused by alcohol are involved in this process. Emerging neurobiological evidence suggests that donepezil, an anticholinesterase agent, may improve AUD treatment outcomes by enhancing neurocognitive functioning. Previous research has also suggested that cognitive remediation therapy (CRT) could potentially improve cognitive function and AUD treatment outcomes. We present the rationale and design of a trial to evaluate the combination of donepezil and cognitive remediation therapy (donepezil + CRT) as an intervention for AUD. Methods: We propose a 13-week, randomized, double-blind, placebo-controlled, between-subjects trial comparing 4 groups (donepezil + CRT vs. donepezil alone vs. CRT alone vs. placebos) as an intervention for AUD. The main goal of the study is to evaluate if donepezil + CRT is superior to placebo in reducing heavy drinking days and improving neurocognitive functioning. A total of 160 patients (4 groups, 40 per each group) with AUD between the ages of 18-80 years will be recruited at Yale University and the VA Connecticut Healthcare System. Primary outcome measures include 1) heavy drinking by Timeline Follow Back (TLFB) over 13 weeks and 2) global neurocognitive functioning by a global index of neurocognitive function score at 7 and 13 weeks. Discussion: This protocol paper describes the rationale and proposed methods for the randomized controlled trial for improving AUD treatment outcomes. This project has significant clinical potential to help patients suffering from AUD by improving their cognition and reducing alcohol consumption. Trial Registration: NCT05042102
引用
收藏
页数:7
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