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Effects of Different Exercise Training Regimens on Visceral Fat Dynamic and Resting Energy Expenditure in Obese Patients

U

University of Leipzig

Status

Unknown

Conditions

Abdominal Obesity

Treatments

Procedure: exercise training

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

In this project, the investigators will test the hypothesis that predominant (two to three times a week 60 min) strength training is more effective in reducing visceral fat mass than endurance training in obese patients.

Full description

Strength training (ST) was shown to be more effective than endurance training (ET) in improving glycemic control in the treatment of type 2 diabetes. However, it is unknown, whether different training strategies have different effects on the preferential visceral adipose tissue reduction and changes in resting energy expenditure in a population with abdominal obesity. We will therefore compare ST and ET (two to three times a week, 60 minutes per training session) in addition to a restricted energy intake of 1500kcal per day for women and 1800kcal per day for men in a prospective study of 200 individuals with abdominal obesity defined by a waist circumference > 102 cm for males and > 88 cm for females and a BMI > 35 kg/m² with regard to:

  1. Abdominal visceral adipose tissue area dynamic (MRI studies)
  2. Abdominal subcutaneous adipose tissue area dynamic (MRI studies)
  3. Total body fat mass changes (bioelectrical impedance analysis)
  4. Changes in resting energy expenditure (indirect calorimetry)
  5. Changes in parameters of glucose metabolism, insulin sensitivity and lipid profile
  6. Changes in circulating adipokines and markers of inflammation In addition, we will search for novel serum parameters, which predict the individual training response by a serum metabolomics/ proteomics approach.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • BMI >= 35 kg/m2
  • waist circumference >102cm (men), >88cm (women)
  • age 18 - 60 years
  • written informed consent

Exclusion criteria

  • type 1 or type 2 diabetes
  • fasting plasma glucose >= 6.0 mmol/l
  • 2h-OGTT (oral glucose tolerance test) glucose >= 11.1 mmol/l
  • any chronic inflammatory or malignant disease
  • medical treatment which influences glucose metabolism
  • drug or alcohol abuse
  • psychiatric disorders
  • untreated thyroid dysfunction
  • cardiac pacemaker or other contraindication for MRI
  • attendant therapy with oral antidiabetic medication, GLP-1 mimetics or analoga, Insulin, anti-obesity medication (orlistat, sibutramine), Falithrom, antipsychotic drugs, any chemotherapeutics
  • pregnant or nursing women
  • expected low compliance
  • current participation in another investigational trial
  • last exercise training <= 6 months ago

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

endurance training
Active Comparator group
Description:
Endurance training: Supervised, twice a week, each training session consists of a 20 min warm up and cool down period and a minimum of 40min tread mill, rawing device or bicycle training. During the study period of 24 months, we will perform an open randomized, prospective training intervention study comparing the effects of three times a week either strength or endurance training on reduction of visceral fat area as determined by MRI scans at the level of L4-L5.
Treatment:
Procedure: exercise training
strength training
Active Comparator group
Description:
Strength training: Supervised, twice a week, each training session consists of a 20 min warm up and cool down period and a minimum of 40min circle training During the study period of 24 months, we will perform an open randomized, prospective training intervention study comparing the effects of two to three times a week either strength or endurance training on reduction of visceral fat area as determined by MRI scans at the level of L4-L5.
Treatment:
Procedure: exercise training

Trial contacts and locations

1

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Central trial contact

Matthias Blüher, prof., MD; Nicole Bauernfeind

Data sourced from clinicaltrials.gov

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