healthy participants
Conditions
Interventions
Group 1: investigation procedures: spiroergometry, recording physiological performance parameter
3 assessment points in 3 weeks, random order (seated, semi-recumbent, recumbent)
Group 2: Further implementation (amendment):
investigation procedures: spiroergometry, recording physiological perform
3 assessment points in 3 weeks, random order (ramp test, incremental test I, incremental test II)
Sponsors
Universitätsklinik Freiburg
Medizinische Klinik
Abt. Rehabilitative und Präventive Sportmedizin
Eligibility
Sex/Gender
All
Age
20 Years to 80 Years
Inclusion criteria
Inclusion criteria: healthy adults (age 20-80), signed informed consent
Exclusion criteria
Exclusion criteria: medical recommendation to avoid intensive load, acute or chronic restrictions on health or medical conditions, that argue against intensive load (infections, acute allergy, disease of the digestive system, of the cardiovasculare system or lungs, aches or fever)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| performance at the individual anaerobe threshold (IAS) in Watt | — |
Secondary
| Measure | Time frame |
|---|---|
| economy of movement on the basis of following parameters: blood lactate concentration (mmol/l), workload (watt, watt/kg), heart rate (bpm), maximal oxygen uptake (VO2max), Rates of perceived exertion (RPE, Borg scale) | — |
Countries
Germany
Contacts
Public ContactAnja Wehrle
Universitätsklinik Freiburg Medizinische Klinik Abt. Rehabilitative und Präventive Sportmedizin
Outcome results
None listed