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RECRUITING
NCT05042102
PHASE2

Donepezil and Cognitive Training for Alcohol Use Disorder (AUD)

Sponsor: VA Connecticut Healthcare System

View on ClinicalTrials.gov

Summary

The goal of the project is to evaluate whether donepezil + cognitive remediation therapy is superior to placebo in reducing heavy drinking in patients with alcohol use disorder in a double-blind, placebo-controlled trial.

Official title: The Combination of Donepezil and Cognitive Training for Treating Alcohol Use Disorder

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2022-08-08

Completion Date

2027-05-31

Last Updated

2025-09-19

Healthy Volunteers

No

Interventions

COMBINATION_PRODUCT

Donepezil + Cognitive remediation therapy (CRT)

Subjects in this arm will receive (1) donepezil and (2) cognitive remediation therapy (CRT). Subjects will take 5 mg/day of oral donepezil in the evening for the first 4 weeks, then 10 mg/day of oral donepezil in the evening until week 13.

COMBINATION_PRODUCT

Donepezil + Placebo CRT

Subjects in this arm will receive (1) donepezil and (2) placebo CRT. Subjects will take 5 mg/day of oral donepezil in the evening for the first 4 weeks, then 10 mg/day of oral donepezil in the evening until week 13.

COMBINATION_PRODUCT

Placebo medication + Cognitive remediation therapy (CRT)

Subjects in this arm will receive (1) placebo medication and (2) cognitive remediation therapy (CRT). Subjects will take placebo oral medication in the evening for the first 4 weeks, then placebo oral medication in the evening until week 13.

COMBINATION_PRODUCT

Placebo medication + Placebo CRT

Subjects in this arm will receive (1) placebo medication and (2) placebo CRT. Subjects will take placebo oral medication in the evening for the first 4 weeks, then placebo oral medication in the evening until week 13.

Locations (1)

VA Connecticut Healthcare System

West Haven, Connecticut, United States