Clinical trial for High Intensity Interval Training (HIT) after bariatric surgery
Not Applicable
- Conditions
- E66.0Obesity due to excess calories
- Registration Number
- DRKS00024939
- Lead Sponsor
- niversitätsklinikum Mannheim
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
Planned Roux-en-Y Gastric bypass or sleeve gastrectomy as bariatric surgery at University Hospital Mannheim
- Male and female patients between the ages of 18 and 80 years
- written consent
- physical ability to complete a bicycle ergometry test
- BMI >/= 35 kg/m^2 in combination with a relevant comorbidity as mentioned in the S3 guidelines for obesity or BMI >/= 40kg/m^2
Exclusion Criteria
- Participation in another clinical trial interfering with this trial
- physical disability not allowing training sessions (e.g. Arthritis, muscular disease)
- Pregnancy and breastfeeding
- severe cardiac or pulmonary disease
- expected non-compliance
- language barrier or failed consent
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Feasibility of a training protocol defined via completion of all trainings with a missing out or early termination of a maximum of four training units in total
- Secondary Outcome Measures
Name Time Method Chance in lactate tolerance, Change in bicycle ergometry maximum strength and heart rate, Change in Borg's scale, Change of nutritional status and inflammatory markers measured in peripheral blood draws