Study of the Drivers of Late Diagnosis of Alcohol Related Diseases, Alone or in Combination With Metabolic Dysfunconal Associated Fatty Liver Disease, Implementation and Evaluation of Itnerventions to Reduce Its Burden.

NCT06403332 | Recruiting

• 1 other identifier: PR(AG)30/2023
• Study Type: interventional
• Target: 350
• Locations: 1 country
• Sites: 2

Brief Summary

Excessive alcohol use is a leading risk factor for preventable disability and death. Alcohol-related liver disease (ALD) is one of the better-known detrimental consequences of alcohol abuse and is the main cause of disability-adjusted life years (DALYs) in European adults. ALD is the main cause of cirrhosis globally and is responsible for 60% of cirrhosis in Europe and North America. Importantly, another etiology of liver disease is on the rise due to the epidemics of obesity and diabetes mellitus in Western countries, i.e., metabolic dysfunction associated fatty liver disease (MAFLD). ALD and MAFLD are largely shaped by social determinants of health (SDH) and lead to mounting health inequalities. Moreover, ALD is subject to strong stigmatization, particularly amongst women, which often leads to lack of inquiry by health professionals. Alone or in combination (MAFLD-OH), both diseases represent a challenge for epidemiologists, clinicians and policy makers in charge of health systems' organization. One of the hurdles to reduce the burden of ALD is the lack of early detection of asymptomatic liver disease among patients with alcohol use disorder (AUD) and heavy drinkers. The only measure that has been proven effective in any phase of the disease is to either stop, compensate, or reverse the liver disease progression, is alcohol abstinence. We hypothesize that establishing effective screening programs to identify patients with ALD and related disorders, coupled with effective treatment will lead to more positive outcomes in prognosis. The central aim of the StopALD Project is to identify patients with advanced ALD during the asymptomatic phases of the disease, as well as identifying the factors related with the lack of early detection to better implement interventions so to tackle both the lack of early detection of ALD and heavy drinking patterns among young people before ALD occurs.

Conditions

Alcohol-related Liver Disease; Alcohol Use Disorder; Metabolic and Alcohol Related/Associated Liver Disease; Metabolic Disfunction Associated Steatotic Liver Disease

Outcome Measures

Primary Outcomes (2)

• efficacy of medical interventional and psychologist

  To assess the efficacy of medical intervention including a hepatology visit, brief intervention and counseling provided by a psychologist as well as the non-invasive assessment of underlying fibrosis degree (Fibroscan improvement of 2 or more points) on alcohol abstinence (assesses by autoreport number of standard units of alcohol) and relapses compared to current standard of care.

  1.5 years

• to assess the efficacy of an in-situ psychologist counseling including a motivational interview among young patients with heavy drinking on alcohol abstinence and relapses compared to current SOC

  to assess the efficacy of an in-situ psychologist counseling including a motivational interview among young patients with heavy drinking on alcohol abstinence and relapses compared to current SOC (alcohol intake assessed by number of standard drinks)

  1.5

Secondary Outcomes (6)

• to assess the impact of the intervention on the underlying liver disease (fibrosis and steatosis degree and rate of complications/decompensations).

  1.5 years

• to investigate the prevalence of MAFLD-OH amongst these patients and whether metabolic risk factors increase the prevalence and severity at diagnosis of advanced liver fibrosis in patients with AUD or excessive alcohol intake

  1.5 years

• to identify the risk factors associated to the late diagnosis of advanced liver disease in patients with compensated vs. decompensated ALD

  1.5 years

• to identify the risk factors associated to the late diagnosis of AUD in young population under 30yo

  1.5 years

• to analyze the associations between sociocultural determinants of alcohol-related issues in the healthcare system and the late diagnosis of AUD, excessive alcohol intake and ALD

  2 years

Study Arms (7)

Cohort A intervention

EXPERIMENTAL

Behavioral: brief intervention

Cohort A non intervention

NO INTERVENTION

Cohort B intervention

EXPERIMENTAL

Behavioral: brief intervention

Cohort B no intervention

NO INTERVENTION

Control grup no significant liver disease

NO INTERVENTION

Control group MASLD

NO INTERVENTION

Control group decompensated ArLD

NO INTERVENTION

Interventions

brief intervention BEHAVIORAL

The intervention for cohort A (intervention arm) based on brief intervention on alcohol consumption performed by a psycologist, medical visit peformed by an hepatologist including assessment of underlying liver disease with non invasive test (i.e Fibroscan and lab work).

Also known as: Diangostic test, Hepatology evaluation

Cohort A intervention; Cohort B intervention

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

Never decompensated patients with ArLD suspicion * Age over 30 * Diagnosis of AUD identified by the AUDIT test or excessive alcohol consumption, i.e., suspicion of current or recent (within one year) AUD or persistent alcohol intake of more than 40 g/daily for women and 60 g/daily for men based on medical history or self-reported history of excessive alcohol use, stigmata of alcohol use on physical exam, liver chemistry abnormalities, and/or alcohol-induced organ involvement other than decompensated liver disease * Alanine (ALT) and aspartate aminotransferases (AST) \<5 times upper normal limit * Bilirubin \<3 mg/dL or/and * AST/ALT ratio \>1.5 or/and * GGT \>100 mg/dL • Patients with a past history of decompensated advanced liver disease (i.e., episodes of jaundice, ascites, hepatic encephalopathy, variceal bleeding, hepatorenal syndrome) or known HCC * Patients with severe extrahepatic disease or terminal illness Young patients with risk alcohol intake and without liver disease * Age between 18-30 years * Diagnosis of AUD identified by the AUDIT test or for whom there is a high suspicion of current or recent (within one year) AUD or persistent alcohol intake of more than 40 g/daily for women and 60 g/daily for men based on medical history or self-reported history of excessive alcohol use, stigmata of alcohol use on physical exam and/or alcohol-induced organ involvement other than decompensated liver disease * Normal liver test including AST, ALT, bilirubin and GGT. • Patients with a past history of decompensated advanced liver disease (i.e., episodes of jaundice, ascites, hepatic encephalopathy, variceal bleeding, hepatorenal syndrome) or known HCC * Patients with severe extrahepatic disease or terminal illness Previously or currently decompensated patients • Age over 30 * Diagnosed ALD with a current or previous liver-related decompensation (i.e., ascites or edemas, hepatic encephalopathy, hepatocellular carcinoma, upper gastrointestinal bleeding, spontaneous bacterial peritonitis or alcoholic hepatitis) • Terminal illness with less than 6 months live expectancy (except advanced hepatocellular carcinoma) * Previous liver transplant recipient Patients without significant liver disease * Age over 30 * Alcohol intake of \<10g per day without current or previous AUD or heavy alcohol intake • Significant liver pathology MASLD patients with a maximum alcohol intake of 20g per day. * Age over 30 * Alcohol intake (\<20g/day in women and \<30g/day in men), * Patients with obesity and/or diabetes mellitus type 2 and/or metabolic syndrome defined by the presence of two or more of the Eslam et al. criteria. • Patients with a past history of decompensated advanced liver disease (i.e., episodes of jaundice, ascites, hepatic encephalopathy, variceal bleeding, hepatorenal syndrome) or known HCC * Patients with severe extrahepatic disease or terminal illness

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

• Hospital Universitari Vall d'Hebron Research Institute: lead
• Universitat Pompeu Fabra: collaborator
• IDIAPJgol: collaborator

Study Sites (2)

Hospital Universitari Vall d'Hebron

Barcelona, 08035, Spain

RECRUITING

University Hospital Vall d'Hebron

Barcelona, 08035, Spain

RECRUITING

MeSH Terms

Conditions

Alcoholism

Interventions

Crisis Intervention

Condition Hierarchy (Ancestors)

Alcohol-Related Disorders; Substance-Related Disorders; Chemically-Induced Disorders; Mental Disorders

Intervention Hierarchy (Ancestors)

Psychotherapy; Behavioral Disciplines and Activities

Central Study Contacts

Portollano

CONTACT

634 832 759; cristina.portellano@vhir.org

Sala

CONTACT

634 833 106; gestio.projectes@vhir.org

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: SCREENING
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 24, 2024
• First Posted: May 7, 2024
• Study Start: February 2, 2023
• Primary Completion: June 6, 2024
• Study Completion: December 6, 2024
• Last Updated: May 7, 2024

Record last verified: 2024-05

Locations

ES (2)