WIRUS: Workplace Interventions Preventing Risky Use of Alcohol and Sick Leave

Sponsor
University of Stavanger (Other)
Overall Status
Unknown status
CT.gov ID
NCT03466541
Collaborator
Kompetansesenter rus - region vest Stavanger (KoRus) (Other), Stamina Helse (Other), Presenter (Other), University of Oslo (Other), Oslo Metropolitan University (Other), Alcohol and Drug Research Western Norway (KoRFor) (Other), Norwegian Institute of Public Health (Other)
500
1
3
72
6.9

Study Details

Study Description

Brief Summary

The aim of this study is to investigate the effectiveness of two workplace interventions (the Riskbruk model and Balance) in reducing risky alcohol consumption, sickness absence and presenteeism. The purpose is to assess whether the Riskbruk model should be implemented in the Norwegian workforce in its entirety, whether the less extensive and costly alternative Balance is sufficient, or if neither one of them show effectiveness compared to usual care.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Riskbruk
  • Behavioral: Balance
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Workplace Interventions Preventing Risky Use of Alcohol and Sick Leave
Study Start Date :
Aug 1, 2013
Anticipated Primary Completion Date :
Aug 1, 2019
Anticipated Study Completion Date :
Aug 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Riskbruk

The employees randomised to the Riskbruk group will be offered two consultations a ∼15 min with the OHS. The subjects will receive individual feedback on the screening results. During these sessions, Motivational Interviewing will be used.

Behavioral: Riskbruk
The Riskbruk model incorporates alcohol screening through a widely employed alcohol screening questionnaire, the Alcohol Use Disorders Identification Test (AUDIT) and a standard alcohol biomarker, carbohydrate-deficient transferring in serum (CDT), with brief consultations using the motivational interviewing (MI) technique. MI is a collaborative conversation style used to increase awareness and reflection around one's own drinking habits, as well as strengthening the person's motivation for a lifestyle change. The conversation style includes expressing empathy through reflective listening, communicating respect and acceptance of the participants and their feelings, and open up for self-reflection and exploration around the drinking behaviour.

Experimental: Balance

The group allocated to the Balance intervention will follow a comprehensive multi-session eHealth intervention with personalised feedback on the screening results.

Behavioral: Balance
Balance is a new Norwegian eHealth programme, and incorporates two approaches to behaviour modification interventions: a brief interventions and an intensive self-help programme. The intervention is based on cognitive-behavioural and self-help principles, and is given to the participants through multiple interactive sessions.

No Intervention: Control group/usual care

The control group will receive the usual follow-up provided by the OHS for persons with risky alcohol behaviour. In order to provide something that appears as a plausible follow-up to the control participants, they will be given a booklet that covers general information about alcohol and potential risks and harms of drinking. The booklet contains no advise on how to achieve a change in drinking behaviour.

Outcome Measures

Primary Outcome Measures

  1. Change in alcohol consumption [Baseline and 6 months]

  2. Change in sickness absence [Baseline and 6 months]

Secondary Outcome Measures

  1. Change in presenteeism [Baseline and 6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Employees screening positive for at-risk drinking (8+ on the AUDIT)
Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Stavanger Stavanger Rogaland Norway 4021

Sponsors and Collaborators

  • University of Stavanger
  • Kompetansesenter rus - region vest Stavanger (KoRus)
  • Stamina Helse
  • Presenter
  • University of Oslo
  • Oslo Metropolitan University
  • Alcohol and Drug Research Western Norway (KoRFor)
  • Norwegian Institute of Public Health

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Stavanger
ClinicalTrials.gov Identifier:
NCT03466541
Other Study ID Numbers:
  • AA0000
First Posted:
Mar 15, 2018
Last Update Posted:
Mar 15, 2018
Last Verified:
Mar 1, 2018
Keywords provided by University of Stavanger
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 15, 2018