Clinical trial Recruiting at 1 site Observational Ages 20 to 80

Impact of MASLD on frailty, cognition, and quality of life by gender

Official title: IIBSP-MAS-2025-133

Run by Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau · NCT07652892 · Data updated 2026-11-12

This study looks at whether frailty differs between men and women with MASLD and how it relates to health, function, hormones, and social factors.

More Steatosis of Liver trials

Quick facts

Study typeObservational
Ages20 Years to 80 Years
SexAll
Enrollment140 (estimated)
SponsorFundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Academic / other
Locations2 sites (Barcelona, Barcelona and 1 other locations)
StatusRecruiting
StartedMay 26, 2026
Main results expectedFebruary 25, 2027
Study endsMay 25, 2028
Registry record updatedJune 17, 2026
Trial IDNCT07652892 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with MASLD who can provide informed consent and participate in periodic assessments, and who do not have exclusionary liver diseases or high-risk alcohol use.

Probably not a fit

Patients with advanced neurodegenerative diseases, severe psychiatric disorders, or significant comorbidities that may overshadow MASLD-related frailty may not benefit from the study findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational study exploring how MASLD-related frailty presents and evolves in men and women. Researchers will examine associations between frailty and clinical, functional, hormonal, and social parameters. The study collects periodic assessments to understand gender-specific differences in prevalence and characteristics. No interventions are being tested; the focus is on describing patterns and potential relationships. The lead site is Hospital de la Santa Creu i Sant Pau in Barcelona, with collaboration across the same institution.

Why it matters

Potential benefit: Findings could improve understanding of gender differences in MASLD-related frailty and guide personalized care approaches.

How similar studies have gone: Previous research in related liver and metabolic conditions has identified gender-specific patterns in frailty and quality of life, supporting the relevance of this observational approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients will be included who are able to provide informed consent and actively participate in periodic assessments.

Exclusion Criteria:

* Risky alcohol consumption:

\> 30 g/day in men and \> 20 g/day in women. AUDIT score: \> 7 points in men, \> 5 in women.

* Other liver diseases (viral hepatitis, autoimmune hepatitis, etc.).
* Advanced neurodegenerative diseases or severe psychiatric disorders.
* Severe comorbidities or treatments that, in the researchers' judgment, may affect frailty and quality of life more than metabolic syndrome and liver disease.

Where it's running

  • Hospital de la Santa Creu i Sant Pau
    Barcelona, Barcelona, Spain
    Recruiting
  • Hospital de la Santa Creu i Sant Pau
    Barcelona, Barcelona, Spain
    Not yet recruiting

Study contacts

  • Principal investigator: Eva Roman — Institut de Recerca IR Sant Pau
  • Study coordinator: Eva Román, Digestive Pathology Nurse
  • Email: ERoman@santpau.cat
  • Phone: 0034630818580

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • Does fructose worsen metabolism and liver inflammation in people with MASH?

    This test looks at whether short-term dietary fructose changes metabolism and increases liver inflammation in people aged 45–65 with MASH, people with simple fatty liver (steatosis), and healthy controls.

    Recruiting at 2 sites Queen Mary University of London · London and 1 other locations · NCT07013916

  • Screening patients at risk for liver disease in Europe

    This study is trying to find out if screening high-risk patients in Europe for liver disease using simple tests can help doctors identify and better understand conditions like metabolic dysfunction-associated steatotic liver disease.

    Recruiting at 6 sites Julius Clinical · Brussels, Vlaams-brabant and 12 other locations · NCT05651724

  • A registry for studying Non-Alcoholic Fatty Liver Disease in Europe

    This study is collecting health information and samples from people with Non-Alcoholic Fatty Liver Disease to learn more about the disease and find better ways to track its progress.

    Recruiting at 33 sites Newcastle University · Antwerp and 36 other locations · NCT04442334

  • Probiotic supplement plus lifestyle changes for fatty liver (MASLD)

    This trial will test whether taking a probiotic supplement alongside lifestyle changes can reduce liver fat, improve liver tests, and improve metabolic health in adults with MASLD.

    Recruiting Fu Jen Catholic University Hospital · New Taipei City and 1 other locations · NCT07400367

  • Ultraportable Hepatoscope ultrasound for measuring liver fat in MASLD/MASH

    The Hepatoscope device will be tested to see if it can measure liver fat accurately in adults with MASLD/MASH compared with MRI-PDFF.

    Recruiting at 2 sites E-Scopics · Angers and 2 other locations · NCT06661655

  • Pre-hepatectomy rehabilitation with mazdutide for obese MASLD donors

    This trial tests whether adding mazdutide to a structured lifestyle plan helps overweight MASLD donors lose liver fat faster to become eligible for donation.

    Recruiting Phase 4 West China Hospital · Hefei, Anhui and 3 other locations · NCT07718126

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.