A preliminary test to examine the efficacy and safety of web-based brief intervention (ALMIGHT brief) for high-risk drinkers

Not Applicable

• Conditions: Heavy drinker

• Registration Number: JPRN-UMIN000040666
• Lead Sponsor: CureApp, Inc.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-06-08
• Study Completion: 2021-03-26
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up continuing
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

Not provided

Exclusion Criteria

(1) Those whose Heavy Drinking Days (Heavy Drinking Day: HDD, 61 + g/day in men and 41 + g/day in women) Is less than 6 in the 4 weeks prior to the screening (2) Those who have five straight non-drinking days in the 4 weeks prior to the screening (3) Those who participated in an alcohol use disorder treatment or drinking reduction support program or self-help group in the four weeks prior to screening (4) Those who had received other structured psychotherapy in the four weeks prior to screening (5) Those with intellectual disability or dementia (DSM-5) (6) Those who used incompatible drugs in the 4 weeks prior to screening (7) Those with clinically serious and unstable complications. (8) Those who has had a history of alcohol withdrawal delirium or convulsive seizures due to alcohol withdrawal. (9) Those with a history of epilepsy or a history of seizures. (10) Those with significant rarefaction at the time of the screening or at the start of the intervention (11) Those who have been judged to be at serious suicide risk by the principal investigator or co-investigators (12) Those who drive vehicles with their main job, or who are engaged in hazardous occupations such as operating machinery or working at height (13) Those who participated in any clinical trial in the 4 weeks prior to the screening (14) Those who do not have a fixed address or telephone number (15) Those who do not routinely use a smartphone installed with iOS 13.0 or higher (16) Those who do not use the LINE messaging app on their smartphones (17) Those who has been judged to be not suitable for the subject of this this study by the principal investigator

Study & Design

• Study Type: Interventional
• Study Design: Not specified