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Secondary and Tertiary Digital Prevention of Non-alcoholic and Dysmetabolic Liver Disease

Secondary and Tertiary Digital Prevention of Non-alcoholic and Dysmetabolic Liver Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06879236
Acronym
CALIBRE
Enrollment
252
Registered
2025-03-17
Start date
2025-01-16
Completion date
2028-01-01
Last updated
2026-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

NAFLD, NASH

Brief summary

The prevalence of Metabolic dysfunction-associated steatotic liver disease (MASLD) and its severe form, Metabolic dysfunction-associated steatohepatitis (MASH), is high and they are increasingly becoming major causes of cirrhosis, hepatocellular carcinoma (HCC), and the need for liver transplantation. Due to the lack of noticeable symptoms during the early stages, the detection of MASLD is often delayed until the disease has advanced. Currently, the treatment options MASLD are limited to lifestyle interventions such as dietary changes and physical activity. Despite the increasing prevalence of MASLD, there are no drugs available on the market specifically for this condition. The goal is to made new model care which integrates the standard clinical procedures with a digital approach, namely a mobile application for patients and a clinical dashboard for healthcare professionals (HCPs), integrated with simple clinical data (anthropometric, laboratory and imaging data). This study wants to test the feasibility of integrating a digital intervention to improve the patient engagement and linkage to care in order to identify the advanced MASLD at earliest stage (secondary prevention) and mitigate the impact of ongoing advanced liver disease helping patients to manage the long-term effect of disease. To achieve this goal the study will leverage on a mobile app named OpenTele in order to test the adherence to lifestyle changes in patient with MASLD and on the connected clinical dashboard. The app aims at integrating the standard clinical practice with digital technologies able to guide and support patients in order to seamlessly integrate secondary prevention strategies in their everyday life with 2 main aims: * to implement a strategy for delay progression of liver disease; * to reduce the effect of cirrhosis (tertiary prevention).

Interventions

None listed

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed with MASLD and LSM\>= 10 kPa * Age \>= 18 years old * Sufficient digital literacy or supported from a caregiver with sufficient digital literacy * Smartphone (Android or iOS) able to download and run the App * Able to understand and communicate in Italian * Able to sign the informed consent

Exclusion criteria

* Major psychiatric disorder * Not able to use digital technologies

Design outcomes

Primary

MeasureTime frameDescription
App Adherence (>80% over 4 weeks)4 weeksAssessed via smartphone (number of app access)

Secondary

MeasureTime frameDescription
Weight reduction assessment12 monthNumber of subjects with a 12-month reduction between 7-10% of weight compared to baseline
Change in liver and spleen stiffnessBaseline, after 4 weeks and 12 monthAssessed by transient elastography
Change in Patient Reported Outcome questionnaire12 weeksEvaluation of overall physical well-being through the administration of questionnaires
Changes in measure energy expenditure12 monthCycle ergometer
Microbiome signature12 monthAnalysis of microbiome signature from feces
Clinical events12 monthRecord of number of hospitalization, decompensation, variceal bleeding, encephalopathy, ascites, liver cancer, liver transplantation, death

Countries

Italy

Contacts

CONTACTLuca Miele
luca.miele@policlinicogemelli.it+390630155701
PRINCIPAL_INVESTIGATORLuca Miele

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026