NCT01208571

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Apr 2011

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 22, 2010

Completed
2 days until next milestone

First Posted

Study publicly available on registry

September 24, 2010

Completed
6 months until next milestone

Study Start

First participant enrolled

April 1, 2011

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2012

Completed
Last Updated

August 30, 2012

Status Verified

August 1, 2012

Enrollment Period

1.7 years

First QC Date

September 22, 2010

Last Update Submit

August 29, 2012

Conditions

Alcohol Use Disorders

Keywords

Harmful useHazardous useDependence

Outcome Measures

Primary Outcomes (1)

  • Alcohol Use Disorder Identification -C (AUDIT-C)

    Alcohol Use Disorder Identification -C. Dicothomous outcome. More or less than four points for women and five points for men.

    6 months

Secondary Outcomes (4)

  • Timeline followback

    6 months

  • Readmissions

    6 months

  • Readiness to Change Questionaire (RTCQ)

    6 months

  • Quality of Life

    6 months

Study Arms (2)

Lifestyle counseling

EXPERIMENTAL
Other: "Booster session"

Treatment as usual

NO INTERVENTION

Interventions

"Booster session"OTHER

Motivational interview

Lifestyle counseling

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Admission with an alcohol related disorder

You may not qualify if:

  • Lack of ability to give informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stavanger University Hospital

Stavanger, 4011, Norway

RECRUITING

MeSH Terms

Conditions

Alcoholism

Condition Hierarchy (Ancestors)

Alcohol-Related DisordersSubstance-Related DisordersChemically-Induced DisordersMental Disorders

Study Officials

  • Kristian Oppedal, MD

    Helse Stavanger HF

    STUDY CHAIR

  • Sverre Nesvaag, Dr

    Helse Stavanger HF

    STUDY DIRECTOR

Central Study Contacts

Åse Cristiansen, RN

CONTACT

+47 05151asci@sus.no

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 22, 2010

First Posted

September 24, 2010

Study Start

April 1, 2011

Primary Completion

December 1, 2012

Study Completion

December 1, 2012

Last Updated

August 30, 2012

Record last verified: 2012-08

Locations

NO(1)