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Vibration Bed Rest Study

Vibration Bed Rest Study - VBR

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00000140
Enrollment
8
Registered
2009-07-13
Start date
2004-06-08
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

muscle atropy, bone resorption, deconditioning of the cardio vascular system, deconditioning of the balance ability, cartilage degeneration

Interventions

Group 1: Subject are immoblized for 14 days using 6° head down tilt bed rest. Twice a day they walk to the training room and stand for 5 x 1 minute on the turned off vibration platform. Inbetween the

Sponsors

Deutsches Zentrum für Luft- und Raumfahrt
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: - healthy male subject - between 18 and 35 years - body weight: 75+/-10 kg - height: 180+/-10 cm - subjects that are willing and have the ability to participate in the whole study - negative skin prick test for sinistrin hypersensitivity - successfully pass the psychological and medical screening

Exclusion criteria

Exclusion criteria: -Abuse of drugs, medicine or alcohol (regular consumption of more than 20 - 30g alcohol / day) -Hyperlipidemia - Adipositas - kidney disorders -Participation in another study within 30 days before study onset -Blood donors in the past three months before the onset of the study -Smoker - Diabetes mellitus - Disposition for keloid -Rheumatic deseases - positive skin prick test for sinistrin hypersensitivity -Bone fractures or severe ligament injuries within one year prior to study onset -Use of metallic implants -Shoe size > 44 -No signed consent form before the onset of the experiment -Every other condition that, in the opinion of the head medical doctor, does not allow a participation in the study

Design outcomes

Primary

MeasureTime frame
Is vibration training able to decelerate or prevent muscle atrophy during 14 days of bed rest? || Changes in Biomarkers of bone metabolism (PINP, bone TRAP, bAP, Osteocalcin, CTX, NTX, Calcitriol) in blood and urine samples Data points: days -3 and -1 befor bed rest, days 2, 6, 8, 11, and 14 during bed rest, days R2 and R3 after bed rest. Blood sampling was performend after overnight fasting each morning at 7:00 am. 24-hour urine samples were collected for each study day || Changes in cartilage thickness of femur and tibia and concentration of biomarker cartialge oligometric matrix protein (COMP) in blood samples; Methods: magnet resonance imaging of the knee joint, biomarkers of cartilage metabolism in blood samples, Data points magnet resonance imaging: study days -1 before bed rest and R1 after bed rest. Data points blood samples: study days -3 and -1 before bed rest, study days 2, 6, 8, 11 and 14 during bed rest, study days R2, R3 and R5 after bed rest. Blood sampling was performed at 7:00 am after overnight fasting. || Changes in balance performance; Method: Investigation of the balance performance using the Posturomed device; Data points: day -4 before bed rest and day R 1 after bed rest.

Countries

Germany

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 2, 2026