Skip to main content
Clinical Trials/NCT01291693
NCT01291693
Completed
Phase 2

Testing Delivery Channels of Brief Motivational Alcohol Intervention Among General Hospital Inpatients With Risky Drinking: Personal Counseling Versus Computer-generated Feedback Letters

University Medicine Greifswald1 site in 1 country975 target enrollmentFebruary 2011

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Hazardous Drinking
Sponsor
University Medicine Greifswald
Enrollment
975
Locations
1
Primary Endpoint
Risky drinking
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The aim of this study is to investigate whether motivation-tailored alcohol interventions are more effective when delivered by person or by computer-generated feedback letters. A sample of 920 general hospital inpatients with risky drinking will be recruited through a computerized screening procedure. Patients with more severe alcohol problems will be excluded from the study. Participants will be allocated by time frame randomization to one of three study arms: (1) personal counseling based on Motivational Interviewing, (2) computer-expert system intervention that generates individualized feedback-letters, and (3) control group (treatment-as-usual). The interventions differ in their channel of delivery, but not regarding their content. Both intervention groups receive interventions at three time points: directly after the baseline-assessment at the general hospital, and 1 and 3 months later by mail and phone, respectively. Outcome will be assessed six, 12, 18 and 24 months after baseline.

Registry
clinicaltrials.gov
Start Date
February 2011
End Date
November 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Medicine Greifswald
Responsible Party
Principal Investigator
Principal Investigator

Dr. Jennis Freyer-Adam

Principle investigator

University Medicine Greifswald

Eligibility Criteria

Inclusion Criteria

  • General hospital inpatients with risky drinking (AUDIT-C \>= 4/5 (women/men) and AUDIT \< 20)

Exclusion Criteria

  • Patients already recruited during an earlier hospital stay
  • Patients physically and mentally not capable of participating in the study
  • Patients with a hospital stay of less than 24 hours
  • Patients with insufficient language/ reading skills
  • Patients employed at one of the departments participating in the study or conducting the study
  • Patients with more severe alcohol problems (AUDIT \>= 20)

Outcomes

Primary Outcomes

Risky drinking

Time Frame: 6, 12, 18, 24 months

Determined by using average alcohol consumption per day, heavy occasional drinking, highest blood alcohol concentration, the Alcohol Use Disorder Identification Test-Consumption (AUDIT-C) score

Secondary Outcomes

  • Motivation to reduce drinking(6, 12, 18, 24 months)
  • Attempts to reduce drinking(6, 12, 18, 24 months)
  • Knowledge about drinking limits(6, 12, 18, 24 months)
  • Self-efficacy scores(6 months)
  • Decisional balance scores(6 months)
  • Self-rated health(6, 12, 18, 24 months)
  • Health care utilization(6, 12, 18, 24 months)

Study Sites (1)

Loading locations...

Similar Trials