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Study identifier: NCT07552727 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Rehabilitation With Exercise-Based Intervention for Nonalcoholic Chronic Hepatic Esteatosis

Condition: Metabolic Adaptation to High-Intensity Interval Training · Metabolic Associated-dysfunction Steatotic Liver Disease (MASLD)  ·  Sponsor: Universidad San Sebastián

PhaseNA
Planned participants30
Who can joinAll sexes, 18 Years to 59 Years
Healthy volunteersNo

About this study

This study proposes a single-blind randomized clinical trial designed to evaluate the effects of high-intensity interval training (HIIT) on liver health in adults with overweight or obesity, while also assessing the usefulness of FibroScan as a tool for detecting and monitoring hepatic changes. The study is grounded in the idea that HIIT may improve liver status in individuals with metabolic dysfunction-associated steatotic liver disease, even in the absence of major weight loss, and that FibroScan could serve not only as a diagnostic method but also as a follow-up instrument during conservative treatment. The sample will include 30 adults from the Los Ríos Region, aged 18 to 59 years, with BMI \>25 kg/m² and chronic noncommunicable conditions such as dyslipidemia, diabetes, or hypertension, provided they are fit for exercise. Participants will be randomly assigned to either an intervention group (HIIT, n=15) or a non-trained control group (n=15). Recruitment will be community-based, using posters and social media, and eligibility will be screened with the PAR-Q+ questionnaire. Individuals with excessive alcohol intake, liver disease of other etiologies, pregnancy, or contraindications to exercise will be excluded. The HIIT intervention will last 8 weeks, with 2 to 3 sessions per week, each session lasting 30 minutes. The protocol consists of five 2.5-minute bouts at 80% of heart rate reserve, interspersed with 2.5-minute active recovery periods at 20% of heart rate reserve…

This description comes directly from the study's public registry record.

Talk to the study team

Sergio Martinez-Huenchullan, PhD  ·  56962859896  ·  sergio.martinez@uss.cl

Always discuss trial participation with your own doctor first.

Locations (1)

Centro de Estudios CientificosValdivia, Los Ríos Region, ChileRecruiting

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Source record: clinicaltrials.gov/study/NCT07552727