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The Effect of a Interdisciplinary Alcohol Cessation Intervention

The Effect of an Interdisciplinary Booster Session in Primary Care Following Brief Intervention in Hospitals - a Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01208571
Enrollment
120
Registered
2010-09-24
Start date
2011-04-30
Completion date
2012-12-31
Last updated
2012-08-30

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

Conditions

Alcohol Use Disorders

Keywords

Harmful use, Hazardous use, Dependence

Brief summary

The effect of alcohol interventions seems to be related to the intensity of the interventions. In this study the investigators will assess the effect of a interdisciplinary booster session in primary care, given to patients who were admitted to hospitals with alcohol related conditions, and who were given Brief Intervention before discharge. The booster session is based on a motivational interview.

Detailed description

The study is a randomized clinical trial, and aims to recruit 60 X 2 patients. Patients admitted to Stavanger University Hospital with an alcohol contributed condition, and who has been given a brief alcohol intervention may be recruited. Candidates for secondary healthcare related to alcohol misuse will be excluded. The interdisciplinary booster session will be given two weeks after discharge, and will be given in the facility of the primary care physician, facilitated by both the physician and an liaison alcohol nurse from Stavanger University Hospital. The intervention is based on motivational interview technique. The primary outcome will be assessed using the Alcohol Use Disorder Identification Test-C, six months after discharge. The outcome assessor will be blinded for the intervention. All outcomes will be collected by telephone interview. The study aims to start recruiting candidates in October-November 2010, and will stoop recruiting in December 2012 at the latest. The study was approved by the national ethical comite in August 2011. The results of the study wil be published in international referee based journals.

Interventions

Motivational interview

Sponsors

Helse Stavanger HF
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Admission with an alcohol related disorder

Exclusion criteria

* Lack of ability to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Alcohol Use Disorder Identification -C (AUDIT-C)6 monthsAlcohol Use Disorder Identification -C. Dicothomous outcome. More or less than four points for women and five points for men.

Secondary

MeasureTime frameDescription
Timeline followback6 monthsGrams og alcohol pr week.
Readmissions6 monthsReadmission to a hospital for an alcohol related and/or a non-alcohol related condition within six months after discharge.
Readiness to Change Questionaire (RTCQ)6 monthsContinous variable
Quality of Life6 monthsSF 12

Countries

Norway

Contacts

Primary ContactÅse Cristiansen, RN
asci@sus.no+47 05151

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026