Hepatic Inflammation and Physical Performance in Patients With NASH

NCT ID: NCT02526732

Last Updated: 2018-09-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

44 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-09-30

Study Completion Date

2017-12-20

Brief Summary

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The aim of the study is to examine the influence of hepatic inflammation or damage on physical performance (maximal oxygen uptake, VO2max) depending on the histologic state of the liver. The study population are patients with fatty liver disease and non-alcoholic steatohepatitis (NASH). All study participants obtain an individual training plan with individual and group training sessions for a period of 8 weeks. At the beginning and end of the training phase a sport physiological examination is carried out. In the study group the effect of regular examinations is surveyed by surrogate parameters of liver inflammation.

Detailed Description

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The study is planned over a period of 24 months. Study participants should be twice examined sport physiologically in a period of 12 weeks. In the study group the influence of regular exercise on surrogate parameters of liver inflammation is investigated over a study period of 8 weeks. Before the exercise all study participants are subjected to a first physiological examination (about 3 hours). This includes a physical examination with detection of body weight, waist circumference and body fat analysis, venous blood, oral glucose tolerance test, ultrasonography of the liver and determination of endothelial function (flow-mediated vasodilatation, FMD) by Doppler analysis. Within 4 weeks after the first examination a sport physical examination is carried out at the Institute of Sports Science at the University of Mainz. This examination contains identification of physical fitness and individual lactate performance diagnostics. In addition, indirect calorimetry is carried out under exercise conditions using spiroergometry to determine the maximal oxygen uptake (VO2max) with special emphasis on the fat metabolism rate at low physical activity. Subsequently to the examination an 8-week training period based on individual training / performance plans is followed. The training plans include independently running exercises for 30-45 minutes two to three times a week. Every two weeks group training sessions are offered accompanied by a sports physician. Within the planed four groups training sessions blood samples will be taken to determinate free circulating DNA and assess lactate values under exercise conditions. After the training phase, a second sport physical examination including physical performance and a final physiological examination including surrogate parameters of liver inflammation are carried out. For statistical analysis, the physical performance of the study participants is examined. Hence patients with histologically proven NASH (NAS score) and confirmed inflammation (increased M30 antigen) are compared to age and gender matched patients with histologically proven fatty liver without inflammation reaction as well as to retrospective data of healthy subjects.

Conditions

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Non-alcoholic Fatty Liver Disease

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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individual training program

Patients will be offered an individual training program. Physical performance and surrogate parameters of liver inflammation will assessed in physical examinations before and after the training phase.

Group Type EXPERIMENTAL

individual training program

Intervention Type OTHER

Training period of 8 weeks: Independently running exercises for 30-45 minutes two to three times a week. Every two weeks group training sessions are offered accompanied by a sports physician.

Interventions

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individual training program

Training period of 8 weeks: Independently running exercises for 30-45 minutes two to three times a week. Every two weeks group training sessions are offered accompanied by a sports physician.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* histologically proven NASH or fatty liver disease

Exclusion Criteria

* bariatric surgery within the last 5 years
* BMI\< 18,5 kg/m2 or \> 45 kg/m2
* heart attack or stroke within the last 6 months
* higher-grade coronary artery disease (CAD III-IV)
* chronic obstructive pulmonary disease (asthma , COPD)
* renal insufficiency
* uncontrolled hypertension or metabolic abnormalities
* alcohol consumption \> 30 g / day (male) and \> 20 g / day (female)
* pregnancy
* concomitant medication able to cause a secondary NASH (eg tamoxifen , corticosteroids )
* concomitant medication able to affect inflammation (eg TNF antagonists)
* concomitant anticoagulant medication (eg phenprocoumon, NOAC)
* other immunological or inflammatory diseases (eg, systemic lupus erythematosus)
* musculoskeletal disorders, preventing sport physiological investigations
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Priv.-Doz. Dr. J. Schattenberg

OTHER

Sponsor Role lead

Responsible Party

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Priv.-Doz. Dr. J. Schattenberg

Prov.-Doz. Dr. med.

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Peter R Galle, MD

Role: STUDY_DIRECTOR

I. Medizinische Klinik und Poliklinik, Universitätsmedizin Mainz

Locations

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University Medical Center of the Johannes Gutenber Univeristy

Mainz, , Germany

Site Status

Countries

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Germany

References

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Huber Y, Pfirrmann D, Gebhardt I, Labenz C, Gehrke N, Straub BK, Ruckes C, Bantel H, Belda E, Clement K, Leeming DJ, Karsdal MA, Galle PR, Simon P, Schattenberg JM. Improvement of non-invasive markers of NAFLD from an individualised, web-based exercise program. Aliment Pharmacol Ther. 2019 Oct;50(8):930-939. doi: 10.1111/apt.15427. Epub 2019 Jul 25.

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Pfirrmann D, Huber Y, Schattenberg JM, Simon P. Web-Based Exercise as an Effective Complementary Treatment for Patients With Nonalcoholic Fatty Liver Disease: Intervention Study. J Med Internet Res. 2019 Jan 2;21(1):e11250. doi: 10.2196/11250.

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Pfirrmann D, Haller N, Huber Y, Jung P, Lieb K, Gockel I, Poplawska K, Schattenberg JM, Simon P. Applicability of a Web-Based, Individualized Exercise Intervention in Patients With Liver Disease, Cystic Fibrosis, Esophageal Cancer, and Psychiatric Disorders: Process Evaluation of 4 Ongoing Clinical Trials. JMIR Res Protoc. 2018 May 22;7(5):e106. doi: 10.2196/resprot.8607.

Reference Type DERIVED
PMID: 29789277 (View on PubMed)

Other Identifiers

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2015_04_001_HELP

Identifier Type: -

Identifier Source: org_study_id

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