Liver health check plus brief alcohol support for hospitalized adults
Official title: Proactive Liver Disease Assessment and Brief Intervention Among Hospitalized People With Harmful Alcohol Consumption: An Investigator-initiated, Pragmatic, Parallel-group, Open-label, 2-arm Randomized Controlled Trial to Investigate the Efficacy of Proactive Elastography-based Brief Alcohol Intervention Compared With Usual Care in Hospitalized Adult Participants at Risk of Alcohol-related Liver Disease
Run by Oslo University Hospital · NCT07637539 · Data updated 2026-11-12
In hospitalized adults who drink harmfully, doctors will test liver stiffness and offer personalized brief alcohol advice to see if it helps reduce drinking compared with usual care.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | Oslo University Hospital Academic / other |
| Locations | 8 sites (Bergen and 7 other locations) |
| Status | Recruiting |
| Started | September 14, 2026 |
| Main results expected | May 15, 2030 |
| Study ends | May 15, 2038 |
| Registry record updated | October 22, 2026 |
| Trial ID | NCT07637539 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18+ admitted for any reason, who drink harmfully (AUDIT-C thresholds) and show moderate to high risk of liver fibrosis (FIB-4 > 1.3).
✕Probably not a fit
Patients without harmful drinking patterns or without liver fibrosis risk may not benefit from elastography-guided counseling.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Adults admitted to 8 Norwegian hospitals who drink at risky levels and have signs of possible liver fibrosis will be randomized to receive liver elastography with tailored brief alcohol intervention or to usual care. Elastography provides a quick liver health assessment at bedside, enabling immediate feedback and personalized counseling about reducing alcohol use. Participants will be followed after discharge at 3, 6, and 12 months to track self-reported drinking, a biomarker (PEth), and quality of life. The study aims to determine whether proactive liver assessment combined with targeted counseling can lower future alcohol-related harm and hospital readmissions. Recruitment targets 500 participants over 18 months.
Why it matters
Potential benefit: If successful, patients may reduce alcohol consumption and slow liver disease progression, potentially lowering future hospitalizations.
How similar studies have gone: Previous brief alcohol interventions have shown modest improvements; the combination with immediate elastography feedback is a novel approach with emerging supportive data.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Emergency hospitalized for any reason in any participating centre 2. Adults 18 years or older 3. Harmful alcohol use, defined as AUDIT-C ≥6 (for men) or AUDIT-C ≥5 (for women) 4. Moderate to high risk of liver fibrosis, defined as FIB-4 \>1.3 5. Signed informed consent Exclusion Criteria: 1. Decompensated liver disease that impedes intervention delivery, defined as one or more of the following: 1. Moderate or severe ascites 2. Overt hepatic encephalopathy (West Haven grade ≥2) 3. Acute-on-chronic liver failure requiring admission to intensive care unit 2. Acute hepatitis of any aetiology, defined as ALT or AST \>5 x upper limit of normal (ULN) 3. Unable to participate for any reason in the opinion of the investigator
Where it's running
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Oslo University Hospital
Oslo, Norway Recruiting -
Haraldsplass Deaconess Hospital
Bergen, Norway Not yet recruiting -
Vestre Viken Bærum Hospital
Drammen, Norway Not yet recruiting -
Sykehuset Nord-Trøndelag Levanger
Levanger, Norway Not yet recruiting -
Sykehuset Innlandet Lillehammer
Lillehammer, Norway Not yet recruiting -
Akershus University Hospital
Lørenskog, Norway Not yet recruiting
Show 2 more locations
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Diakonhjemmet Hospital
Oslo, Norway Not yet recruiting -
Lovisenberg Diaconal Hospital
Oslo, Norway Not yet recruiting
Study contacts
- Principal investigator: Mette Vesterhus — Haraldsplass Deaconess Hospital, Bergen, Norway
- Study coordinator: Håvard Midgard, Professor
- Email: havardmi@gmail.com
- Phone: +47 908 30 071
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.