Ultra-Brief Intervention for general hospital inpatients with high risk drinking habits, single-center quasi-randomized controlled trial

JRCT ID: jRCT1090220426

Registered date:10/06/2019

Basic Information

• Recruitment status: PENDING
• Health condition(s) or Problem(s) studied: Alcohol use disorder
• Date of first enrollment: 19/07/2019
• Target sample size: 100
• Countries of recruitment: Japan
• Study type: Interventional

Intervention(s)

Intervention type:BEHAVIOUR
Name of intervention:Ultra-Brief Intervention
Dose form / Japanese Medical Device Nomenclature:NOT APPLICABLE
Route of administration / Site of application:NOT APPLICABLE
Dose per administration:
Dosing frequency / Frequency of use:
Planned duration of intervention:within 1 minute, only once
Intended dose regimen:We give one leaflet of A4 size and give simple advice and feedback within one minute.
detailes of teratment arms:We give one leaflet of A4 size and give simple advice and feedback within one minute. The intervention is only once.
Comparative intervention name:control
Dose form / Japanese Medical Device Nomenclature:NOT APPLICABLE
Route of administration / Site of application:NOT APPLICABLE
Dose per administration:
Dosing frequency / Frequency of use:
Planned duration of intervention:
Intended dose regimen:We do not intervene.

Outcome(s)

• Primary Outcome: Drinking volume
• Secondary Outcome: AUDIT-C score and days of heavy drinking

Key inclusion & exclusion criteria

• Age minimum: >= 18age old
• Age maximum: <= 75age old
• Gender: Both
• Include criteria: Hospitalized at the trial institutions on July 19, 2019, ages 18 to 75, and AUDIT-C scores 5 or more for men and 4 or more for women
• Exclude criteria: Patients admitted to the intensive care unit or high care unit or maternal-fetal intensive care unit or patients who do not obtain written consent

Related Information

• Primary Sponsor: Yukio Tezuka
• Source(s) of Monetary Support: Japan Agency for Medical Research and Development
• Secondary ID(s): JMA-IIA00426