Muscular atrophy, bone loss, deconditioning of the cardiovascular system, deterioration of the vestibular system, deterioration of cognitive performance, fluid shifts, eye changes, SANS
Conditions
Interventions
Group 1: 2x6 subjects are immobilised for 30 days in a 6° head-down position. They complete 6 x weekly supine bicycle ergometry (45 minutes each, plus warm-up and cool-down) and then another 6 hours w
Sponsors
DLR- Deutsches Zentrum für Luft- und Raumfahrt / Institut für Luft- Und Raumfahrtmedizin
Eligibility
Sex/Gender
All
Age
24 Years to 55 Years
Inclusion criteria
Inclusion criteria: - Male and female, healthy volunteers aged 24-55 years with a body mass index (BMI) of 19-30 kg/m2 and a height of 153-190 cm. - Non-smokers, smoking cessation at least six months prior to study entry - Subjects who are willing and able to participate in the entire study - Present certificate from a health insurance company and police clearance certificate - Successful completion of the medical and psychological inclusion examination - Informed consent available at the beginning of the study - Presentation of a dental certificate
Exclusion criteria
Exclusion criteria: - Any illnesses, injuries or medical conditions that could prevent safe participation in the study or result in a significant bias in the scientific results - Drug, medication or alcohol abuse (regular consumption of more than 30 g alcohol/day). - Need for any form of prescription medication. Exception: hormonal contraceptives, which do not cause a significant increase in the risk of thrombosis. In this case, hormonal contraception must be used for the entire duration of the study. - Smoker (also e-cigarettes, shisha, e-shisha etc.) - Vegetarianism, veganism during the study - Claustrophobia (fear of actual or perceived confinement, fear of confined spaces) - Increased intraocular pressure - Eye problems with a significant impact on vision - Laser eye surgery to correct visual acuity - Severe long-sightedness > +5 dpt. - Astigmatism (astigmatism of the cornea) > 3 dpt. - Significant chronic complaints due to gastro-oesophageal reflux ("heartburn") - Current or past disc herniation - Chronic back pain - Kidney stones, current or past - Increased risk of thrombosis * - Pronounced orthostatic intolerance (blood pressure regulation disorder occurring when changing to an upright position (orthostasis) ) - Current or past bleeding tendency or coagulation disorders. - In female candidates: - Existing pregnancy or breastfeeding - Menopause or post-menopause - Any medical or orthopaedic condition that would interfere with participation in the bed rest or any of the examinations to be performed (e.g. diabetes, severe rheumatism, hypertension requiring treatment, etc.). The decision is up to the study doctor. - Bone density of femur and lumbar spine (L1-4) < -2.0 SD t-score - Metal implants, other osteosynthesis materials, implants, tattoos or permanent make-up which are not MRI compatible or which interfere with examinations due to their location. - Participation in another clinical trial within the last 3 months prior to the start of this study, if the study design conflicts with this study (e.g. certain drug trials) - Chronic tinnitus, severe hearing loss or implanted hearing aid - Allergies to an extent that requires the constant presence of an emergency kit - Any other condition that, in the opinion of the investigator, makes the subject unsuitable for inclusion in the study - Entry in EU and US counter-terrorism databases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Aim of the study: Maintaining the safety and well-being of astronauts is essential for successful future long-term missions aboard the International Space Station (ISS), on the Moon and eventually on Mars. | — |
Countries
Germany
Contacts
Public ContactEdwin Mulder
DLR - Institut für Luft- und Raumfahrt
Outcome results
None listed