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The development and effectiveness of brief interventions for alcohol delivered by community pharmacists

The development and effectiveness of brief interventions for alcohol delivered by community pharmacists: cluster randomized controlled trial - COMPASS-REDUCE: COMmunity Pharmacists ASSist for patients - Reducing Alcohol Use, Cluster Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000056621
Enrollment
231
Registered
2025-01-06
Start date
2025-01-20
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients who have been prescribed antihypertensive drugs or oral diabetes drugs, regularly receive medication at the research-participating pharmacy (for more than 3 months), and are scored 8-14 on the AUDIT (Alcohol Use Disorders Identification Test).

Interventions

Intervention Group A: In addition to the regular medication guidance, provision of 90 bottles of 350mL non-alcoholic beverages (30 bottles, 3 times) and brief interventions for drinking by a pharmacis

Sponsors

Wakayama Medical University
Lead Sponsor
Kyoto University, Graduate School of Medicine, School of Public Health, Department of Preventive Services, Dr.Hiroshi OKADA
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Aged 20 years or older 2) People scored between 8-14 on the AUDIT (Alcohol Use Disorders Identification Test)

Exclusion criteria

Exclusion criteria: 1) People who are receiving treatment for alcohol problems 2)People who are participating in other alcohol-related studies 3)Dialysis patients 4)Pregnant or breastfeeding individuals 5)People who are taking psychiatric medications such as antidepressants, anti-anxiety drugs, antipsychotics (excluding sleep-inducing drugs) 6)People who cannot visit the pharmacy continuously for the research period of 3 months 7)People who do not agree to be contacted by the pharmacist by phone, email, etc. during the research period 8)Others who the principal investigator has judged to be unsuitable for research participation

Design outcomes

Primary

MeasureTime frame
Change in weekly amount of alcohol intake from baseline to 3 months later(g)

Secondary

MeasureTime frame
AUDIT, AUDIT-C, Body weight(kg), BMI, Blood pressure(mmHg), HbA1c, Blood glucose level, WBC, RBC, Hemoglobin, Hematocrit, MCV, AST, ALT, Gamma-GTP Change in weekly amount of alcohol intake from baseline to 6 months later(g) Prescription medication information Knowledge, motivation, and attitudes about the impact of alcohol on health in research participants Knowledge, confidence, and attitudes about drinking reduction support in research participating pharmacists

Countries

Japan

Contacts

Public ContactMayuko KOTANI

Wakayama Medical University School of Pharmaceutical Sciences, Department of Social and Community Pharmacy

kotaccimko@gmail.com090-2444-9442

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026