Actively Recruiting
AlcoTail - Implementation of Tailored Interventions
Led by Oslo University Hospital · Updated on 2025-07-31
4200
Participants Needed
1
Research Sites
324 weeks
Total Duration
On this page
Sponsors
O
Oslo University Hospital
Lead Sponsor
S
St. Olavs Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to investigate the implementation and real-world effects of an intervention for harmful use of alcohol and psychoactive medicinal drugs among hospital inpatients. Due to the negative impact of alcohol consumption on health outcomes, a call for action has been made by the Norwegian Ministry of Health, with focus on screening patients for alcohol consumption and evidence-based tailored interventions for those with medium or high consumption. In addition, non-prescribed use of psychoactive medicinal drugs, or concomitant use with alcohol, can also have negative health effects, therefore improved monitoring of the use of these are warranted. Interventions will be introduced as routine procedures at Norwegian hospitals in the upcoming year, and 2500 patients receiving acute medical care will be included in the control group before the intervention is implemented, and 2500 patients in the case group after the implementation is effectuated. This study will evaluate the implementation process using baseline data on self-reported alcohol- and psychoactive medicine use, motivation to reduce consumption and mental distress. In addition, left-over blood samples used for diagnostic purposes will be collected and analyzed for alcohol, psychoactive medicinal and illicit drugs. After 12 months baseline data will be coupled to patient journal data and relevant registry data in order to evaluate the effects of the intervention.
CONDITIONS
Official Title
AlcoTail - Implementation of Tailored Interventions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients admitted to Medical wards
You will not qualify if you...
- Inability to understand written and verbal Norwegian
- Cognitive or mental inability to consent to participation
- Injury or planned surgery as primary reason for admission
AI-Screening
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Trial Site Locations
Total: 1 location
1
Oslo University Hospital
Oslo, Norway
Actively Recruiting
Research Team
A
Anners Lerdal, PhD
CONTACT
S
Stig Tore Bogstrand, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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