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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06359444
Other study ID # ONZ-2023-0453
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 26, 2024
Est. completion date March 15, 2026

Study information

Verified date June 2024
Source University Hospital, Ghent
Contact Patrick Calders, Prof. dr.
Phone 0032498354766
Email patrick.calders@ugent.be
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common liver disease worldwide, and is associated with obesity and the metabolic syndrome. Physical activity and lifestyle interventions are among the most recommended treatments for individuals with MASLD. In this RCT, we will evaluate the effect of combined exercise training "strength and aerobic training" versus "strength and high intensity training (HIIT)". The main outcome parameter is the severity of liver steatosis. Patients will be recruited at the fatty liver clinic of the UZ Gent.


Description:

Physical activity and lifestyle interventions, including exercise, are recommended for individuals with metabolic dysfunction-associated steatotic liver disease (MASLD). Weight loss has been found to improve MASLD histologically, but exercise alone can also reduce liver fat accumulation, even without significant weight loss. Exercise has positive effects on chronic inflammation, type 2 diabetes mellitus (T2DM), and mitochondrial function in MASLD patients. Studies suggest that both aerobic and resistance exercise are effective in reducing fat content and liver enzyme levels in MASLD, and thereby generate positive effects on insulin sensitivity and cardiovascular risk. The potential of high-intensity interval training (HIIT) is large in various settings, but was never explored in this population. Moreover, the combination with strength training can have additional health effects which remain to be explored. All subjects are recruited in the liver steatosis outpatient clinic of the university hospital in Ghent by the physicians and researchers of this study. After patient selection and obtaining informed consent, they will be screened in the rehabilitation center for cardiorespiratory fitness.


Recruitment information / eligibility

Status Recruiting
Enrollment 92
Est. completion date March 15, 2026
Est. primary completion date March 15, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Diagnosed with MASLD by ultrasound, CAP and/or biopsy - Age between 18 and 75 years old - No significant liver fibrosis (Fibroscan < 7.5 kPa; if it is between >7.5 and <10, there must be absence of liver fibrosis in the biopsy) Exclusion Criteria: - Presence of other liver diseases that may contribute to the clinical presentation in the patient - Severe cardiovascular, orthopedic, physical or other illnesses that make it impossible to participate in the study's exercise rehabilitation program or where safety cannot be guaranteed - Pregnancy - Pharmacological treatment that directly affects MASLD (e.g. GLP-1 analogues) - A change in medication in the last three months before the study that affects metabolic disease stability

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Combined aerobic + strength training
Participants will follow a combination of endurance and strength training for 14 weeks. There will be three sessions every week: two at Ghent university department of rehabilitation and one at home. Each session will last approximately one hour.
Combined strength + HIIT training
6 weeks of endurance training and strength training, 8 weeks of strength training and HIIT. Participants will follow the same combination of endurance and strength training for the first six weeks, to build up to a baseline level of physical fitness. They will then switch to eight weeks of a combination of strength training and High Intensity Interval Training (HIIT). There will be three sessions every week: two at Ghent university department of rehabilitation and one at home. Each session will last approximately one hour.

Locations

Country Name City State
Belgium Ghent University Hospital Ghent

Sponsors (2)

Lead Sponsor Collaborator
University Ghent University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

References & Publications (4)

Hashida R, Kawaguchi T, Bekki M, Omoto M, Matsuse H, Nago T, Takano Y, Ueno T, Koga H, George J, Shiba N, Torimura T. Aerobic vs. resistance exercise in non-alcoholic fatty liver disease: A systematic review. J Hepatol. 2017 Jan;66(1):142-152. doi: 10.1016/j.jhep.2016.08.023. Epub 2016 Sep 14. — View Citation

Karlas T, Petroff D, Sasso M, Fan JG, Mi YQ, de Ledinghen V, Kumar M, Lupsor-Platon M, Han KH, Cardoso AC, Ferraioli G, Chan WK, Wong VW, Myers RP, Chayama K, Friedrich-Rust M, Beaugrand M, Shen F, Hiriart JB, Sarin SK, Badea R, Jung KS, Marcellin P, Filice C, Mahadeva S, Wong GL, Crotty P, Masaki K, Bojunga J, Bedossa P, Keim V, Wiegand J. Individual patient data meta-analysis of controlled attenuation parameter (CAP) technology for assessing steatosis. J Hepatol. 2017 May;66(5):1022-1030. doi: 10.1016/j.jhep.2016.12.022. Epub 2016 Dec 28. — View Citation

Keating SE, Hackett DA, George J, Johnson NA. Exercise and non-alcoholic fatty liver disease: a systematic review and meta-analysis. J Hepatol. 2012 Jul;57(1):157-66. doi: 10.1016/j.jhep.2012.02.023. Epub 2012 Mar 10. — View Citation

Oh S, Tsujimoto T, Kim B, Uchida F, Suzuki H, Iizumi S, Isobe T, Sakae T, Tanaka K, Shoda J. Weight-loss-independent benefits of exercise on liver steatosis and stiffness in Japanese men with NAFLD. JHEP Rep. 2021 Feb 10;3(3):100253. doi: 10.1016/j.jhepr.2021.100253. eCollection 2021 Jun. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Liver steatosis by CAP Liver stiffness measurement will be performed using vibration-controlled transient elastography, more specifically the Fibroscan. This method measures the fat accumulation in the liver (dB/m) and the level of scar tissue (kPa), represented as the CAP or steatosis score and the fibrosis score respectively. before training and after training (14 weeks)
Primary Liver steatosis on ultrasound Ultrasound can demonstrate hepatic fatty tissue, estimating severity based on liver-kidney contrast, resolution loss thv the intrahepatic blood vessels, and visibility of the diaphragm. On this basis, a score 0-3 can be assigned. before training and after training (14 weeks)
Secondary Insulin sensitivity Insulin sensitivity will be assessed by calculation of the HOMA-IR index (fasting glucose x insulin) before training and after training (14 weeks)
Secondary Liver transaminases Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) are enzymes located primarily in liver cells. An elevation of these enzymes in the bloodstream may indicate liver damage or inflammation. before training and after training (14 weeks)
Secondary Maximal exercise test A ramp protocol will be performed starting at 25 watts, adding 25 watts per minute each time.
This test will be administered using ergospirometry to derive measures for aerobic physical condition.
before training and after training (14 weeks)
Secondary Strength Strength will be measured by 1RM determination of the muscle groups that will be trained (leg press, adductors, vertical traction, chest press, abdominal and back muscles). This measurement will be performed at baseline, after 10 weeks and at the end of the study before training and after training (14 weeks)
Secondary Cardiovascular function Blood pressure measurements:
Before and after exercise, systole and diastole blood pressure will be measured. Blood pressure will be measured three times and the average value recorded.
before training and after training (14 weeks)
Secondary Weight Weight will be measured using a scale to the nearest 0.1 kilogram (kg). before training and after training (14 weeks)
Secondary Heigth Height will be measured to the nearest 0.1 meter (m) with a stadiometer. before training and after training (14 weeks)
Secondary BMI BMI will be calculated. before training and after training (14 weeks)
Secondary waist Waist circumference is measured in standing position with a measuring tape just above the iliac crest, to the nearest 0.1 centimeter (cm). before training and after training (14 weeks)
Secondary BIA Bioelectrical impedance analysis (BIA) will be performed to determine lean mass and fat percentage. before training and after training (14 weeks)
Secondary Interleukine IL-6 and IL-8 serum levels will be measured in blood. These are correlate with the progression of liver fibrosis and are elevated in patients with chronic liver disease. before training and after training (14 weeks)
Secondary TNF-alfa TNF-a is a pro-inflammatory cytokine produced by macrophages and will be measured in blood. Inflammation in NAFLD causes TNF-a to be released into the body. The amount is increased in patients with NAFLD and correlates with the level of fat mass and insulin resistance. before training and after training (14 weeks)
Secondary Hepatokines Hepatokines will be measured in blood. These are proteins secreted by the liver which have a demonstrated association with metabolic function/dysfunction. These include fetuin-A, FGF-21, follistatin etc. before training and after training (14 weeks)
Secondary Myokines Myokines will be measured in blood. These are proteins secreted by the muscle which have a demonstrated association with metabolic function/dysfunction. These include myostatin, brain-derived neurotrophic factor, etc.... before training and after training (14 weeks)
Secondary Adipokines Adipokines will be measured in blood. These are proteins secreted by the adipose tissue which have a demonstrated association with metabolic function/dysfunction. These include leptin, adiponectin, etc. before training and after training (14 weeks)
Secondary SF-36 Quality of life will be measured using SF-36 (a standard questionnaire). before training and after training (14 weeks)
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