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临床试验/NCT07652151
NCT07652151招募中不适用

UNMASK: Unveiling the Pathobiology of Metabolic Dysfunction-Associated Steatotic Liver Disease for the Discovery of Novel Therapeutics and Biomarkers - Study Protocol Version 2.0

Fundación Pública Andaluza para la gestión de la Investigación en Sevilla3 个研究点 分布在 3 个国家目标入组 450 人开始时间: 2026年1月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
450
试验地点
3
主要终点
Steatosis response

研究概览

简要总结

Overall design: The study will include one intervention based on Mediterranean diet plus structured lifestyle intervention (150 min/week of moderate-intensity or 75 min/week of high-intensity exercise) for a total of 16 weeks. Following a screening period of up to 12 months, eligible participants will be included in a single cohort.

Study details include:

  • Study duration will be up to 36 months including the screening period.
  • Intervention will be up to 16 weeks.
  • Visit frequency will be every 4 weeks for the interventional period and every 12 weeks during follow-up.

详细描述

The UNMASK trial is a multicenter (Spain, Italy and Turkey), prospective, open-label lifestyle intervention based on tailored caloric restriction and monitored exercise. UNMASK aims to prove that the amelioration of MASLD at systemic and hepatic levels will be parallel to the improvement in our selected biomarkers. Given the known challenges with diagnosis and staging of MASH when using histopathological assessments of liver biopsies, the study will evaluate various blood-based non-invasive biomarkers. Non-invasive tests will be performed to asses endpoints. UNMASK includes a single arm in which patients undergo lifestyle changes, chiefly through the prescription of Mediterranean diet and physical exercise.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Metabolic disarrangements following ATPIII criteria (i.e. comorbidities such as Type 2 diabetes, central obesity, BMI≥>25 kg/m2, hypertension, dyslipidaemia.
  • Written informed consent
  • No dietetical counsellor/weight loss higher than 10% within the prior 6 months
  • Age over 18 years old
  • Liver stiffness measurement by Fibroscan ≥ 8, CAP ≥ 248 db/m and MRI PDFF ≥ 5%. ,

排除标准

  • Significant alcohol intake (≥30 g/day in men and ≥20 g/day in women)
  • Other causes of liver disease (evidence of viral or autoimmune hepatitis, HIV, drug-induced fatty liver or other metabolic liver diseases)
  • Use of recreational drugs
  • Decompensated acute or chronic liver disease
  • Cirrhosis or transplant waitlist
  • Pregnancy or parenteral nutrition
  • No nutritional interventions, medications for weight loss or weight loss higher than 5% within the last year
  • Presence of other comorbidities that would impact lifestyle intervention (i. e. prosthesis)
  • Absence of a personal smartphone with a compatible operating system capable of supporting the Amazfit Bip 6 accelerometer app's functionalities: Android 7.0 or iOS 14.0, or later.

研究组 & 干预措施

Multimodal lifestyle intervention

Experimental

Mediterranean diet (MD) rich in olive oil, nuts and coffee, combined with structured exercise through a lifestyle intervention (LSI)

干预措施: Multimodal lifestyle intervention (Behavioral)

结局指标

主要结局

Steatosis response

时间窗: From baseline to month 16

Defined as a 30% decrease in MRI-Proton Density Fat Fraction (PDFF) and CAP assessed by Transient Elastography

Fibrosis regression

时间窗: From baseline to month 16

\>20% reduction in liver stiffness measured by MRE.

MASH resolution

时间窗: From baseline to month 16

According to the non-invasive composite tool MASH Resolution Index (MASH-RI) (Stine et al Hep Comm 2025)

次要结局

  • % Change in Weight(From baseline to month 16)
  • % Change in Waist Circumference(From baseline to month 16)
  • Change in Patient Reported Physical Activity(From baseline to month 16)
  • Change in Patient Reported Diet Habits by MEDAS Questionnaire(From baseline to month 16)

研究者

研究点 (3)

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