Simulated Microgravity by Head Down Tilt BedrestBRACENCT06544213
A 60 Days Head Down Tilt Bedrest With Artificial Gravity and Cycling Exercise on 24 Healthy Male (BRACE)
A study testing Countermeasure Supine Bike and Countermeasure AG-Bike in people with Simulated Microgravity by Head Down Tilt Bedrest and Weightlessness, run by Centre National d'Etudes Spatiales at 1 site in France.
Trial summary
The objective of this study is to investigate whether a cycling exercise coupled with artificial gravity via a short-arm human centrifuge helps to prevent and / or reduce the deleterious effects induced by 60 days of anti-orthostatic bedrest. Read more about this study
- Who is it for?
- Ages 20 to 45 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Simulated Microgravity by Head Down Tilt Bedrest, Weightlessness
- What is being tested?
- Countermeasure Supine Bike and Countermeasure AG-Bike
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 24 participants
- Where
- 1 siteFrance
- Study dates
- 6 Feb 2023to 6 Jun 2026
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 to 45 years
- Men only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Healthy male volunteer (see below the description of medical tests and laboratory analysis performed at the selection visit)
- Aged 20 to 45 years
- No overweight nor excessive thinness with BMI (weight kg/ height m2) between 20 and 27 kg/m2
- Height between 158 and 190 cm
- Certified as healthy by a comprehensive clinical assessment (detailed medical history and complete physical examination): in particular, free from any chronic disease or any acute infectious disease or cardiovascular, neurological, of the ear, nose, throat (especially orthostatic hypotension and vestibular disorders), orthopaedic or musculoskeletal disorders
- Good mental health: tests and psychological interview will be held by a specialist in extreme environment
Show all 12Show fewer
- Fitness level assessment: 35 mL/min/kg < VO2max < 55 mL/min/kg
- Non active smokers
- No alcohol or drug dependence, and no medical treatment
- Covered by a Health Insurance System
- Having signed the information consent
- Free of any engagement during the study
Who cannot join
- Any history or presence of clinically relevant cardiovascular, neurological or ear, nose, throat disease, any chronic disease; any acute infectious disease. Particularly:
- Symptomatic orthostatic hypotension whatever the decrease in blood pressure, or asymptomatic postural hypotension defined by a decrease in systolic blood pressure equal to or greater than 20 mmHg within 3 minutes when changing from the supine to the standing position,
- Cardiac rhythm disorders,
- Hypertension,
- Chronic back pains,
- Vertebral fracture, scoliosis, or herniated disc,
Show all 38Show fewer
- Glaucoma,
- Self-reported hearing problems,
- Vestibular disorders
- History of migraines,
- History of hiatus hernia or gastro-esophageal reflux,
- History of thyroid dysfunction, renal stones, diabetes,
- History of head trauma,
- Abnormal result for lower limbs echo-doppler,
- History of genetic muscle and bone diseases of any kind,
- Past records of thrombophlebitis, family history of thrombosis or positive response in thrombosis screening procedure (anti thrombin III, S-protein, C-protein, factor V Leiden mutation and the mutation 20210 of the prothrombin gene),
- Bone mineral density: T-score ≤ -1.5,
- Poor tolerance to blood sampling,
- Having given whole blood (more than 7 mL/kg) in a period of 8 weeks or less before the start of the experiment, or having given whole blood more than 2 times in the past year,
- Significant history of allergy, especially no dermatological or food allergy,
- Significant anomaly detected in the biological analysis,
- Positive reaction to any of the following tests: hepatitis A immunoglobulin, hepatitis B antigen, anti hepatitis C antibodies, anti Human Immunodeficiency Virus 1+2 antibodies,
- Vegetarian or vegan,
- Refusal to give permission to contact his general practitioner,
- Subject who, in the judgment of the investigator, is likely to be non-compliant during the study, or unable to cooperate because of a language problem or poor mental development,
- Subject already participating or in the exclusion period of a clinical research,
- Subject who has received more than 4500 Euros within 12 months for being a research subject,
- Subject who cannot be contacted in case of emergency,
- Subject who had the two knees injured
- MRI contraindications
- History or active claustrophobia
- Osteosynthesis material, presence of metallic implants or any other contra-indication for MRI
- Vulnerable persons according to French law (L1121-5 to L1121-8) :
- Persons deprived of their liberty by an administrative or judicial decision
- Persons under involuntary psychiatric care
- Persons admitted in a health or social establishment for purposes other than research
- Minors
- Adults subject to legal protection (subject under guardianship or trusteeship) or unable to express their consent
Trial locations and contacts
1 site in 1 country.
France1 site
MEDES-Institut de Médecine et Physiologie Spatiale
Toulouse, France, 31400
About this study
Official title: A Randomized Controlled Study on 24 Healthy Male Volunteers Evaluating the Effects of Centrifugation and Exercise to Prevent the Deconditioning Induced by 60 Days of Head-down Bedrest Used as a Ground-based Model to Mimic Weightlessness.
The objective of this study is to investigate whether a cycling exercise coupled with artificial gravity via a short-arm human centrifuge helps to prevent and / or reduce the deleterious effects induced by 60 days of anti-orthostatic bedrest.
The secondary objective is to investigate whether the combination of a supine cycling exercise with artificial gravity is more effective than the same supine cycling exercise alone in preventing or reducing the effects of head-down bedrest.
Read more
During a randomized, 60 day bed rest study, in 24 healthy male adults, the two following aims will be undertaken:
- Fourteen scientific protocols will assess the changes in the cardiovascular, metabolic, musculoskeletal, neuro-sensorial, haematological, and immunological systems.
- In the above-mentioned systems, the comparative potential beneficial effects of the two countermeasure protocols will also be investigated by the scientific protocols and bedrest standard measurements (BSM).
Read the detailed description
Space flights have shown the possibilities and limitations of human adaptation to space. For the last 60 years, results have shown that the space environment and microgravity in particular, cause changes that may affect the performance of astronauts. These physiological changes are now better known: prolonged exposure to weightlessness can lead to significant loss of bone and muscle mass, strength, cardiovascular and sensory-motor deconditioning, immune, hormonal and metabolic changes .
Moreover, recently a new suite of physiological adaptations and consequences of space flight has been acknowledged. Indeed, after long flights, some astronauts present persistent ophthalmologic changes, mostly a hyperopic shift, an increase in optic nerve sheath diameter and occasionally a papillary oedema now defined by National Aeronautics and Space Administration (NASA) as Spaceflight-Associated Neuro-ocular Syndrome (SANS). Some of these vision changes remain unresolved for years post-flight. This phenomenon has most likely existed since the beginning of human space flight but is just recently being recognized as a major consequence of adaptation to microgravity.
Overall, spaceflight induces physiological multi-system deconditioning which may impact astronauts' efficiency and create difficulties upon their return to normal gravity. Understanding the underlying mechanisms of these processes and developing efficient countermeasures to prevent, limit or reverse this deconditioning remain important challenges and major priorities for manned space programs.
The space agencies are actively engaged in studying the physiological adaptation to space environment through studies on board the International Space Station (ISS) but also on the ground. Indeed, considering the limited number of flight opportunities, the difficulties related to the performance of in-flight experiments (operational constraints for astronauts, limited capabilities of in-flight biomedical devices), ground-based experiments simulating the effects of weightlessness are used to better understand the mechanisms of physiological adaptation, design and validate the countermeasures.
Different methods are used to simulate microgravity on Earth. However, two approaches, -6° head-down bed rest (HDBR) and dry immersion (DI) have provided possibilities for long-term exposures with findings closest to those seen with a weightless state. They produce changes in body composition (including body fluid redistribution), cardiovascular and skeletal muscle characteristics that resemble the effects of microgravity. One of the advantages of the HDBR model is that it has now been used in a great number of studies internationally, and its effects have long been described and compared with those of microgravity and spaceflight. Long-term bedrest is the gold-standard method for studying the effects of weightlessness and to test countermeasures.
The HDBR, as the name implies, implicates a long (from several weeks to a year) stay in the supine position, the head tilted down by -6° from the horizontal plane. HDBR is the most frequently used ground-based simulation for gravitational unloading of the human body in western countries.
During human space missions, the current most effective countermeasure is physical exercise. However, it is both time-consuming and not completely satisfactory. One of the solutions for this is to combine physical exercise with artificial gravity, with the use of a short-arm human centrifuge (SAHC). This study proposes to test the effectiveness of a countermeasure protocol combining Artificial Gravity (AG) with a cycling exercise, and to compare it with only a cycling exercise, and with a complete lack of physical exercise.
- Being tested
- Control Group, Countermeasure Supine Bike, Countermeasure AG-Bike
- Keywords
- Simulation of microgravity, Weightlessness, Artificial Gravity, Bedrest, Countermeasure
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Control GroupBehavioural
60 days of strict head down tilt bed rest at all time. No countermeasure program is performed.
Countermeasure Supine BikeBehavioural
60 days of strict head down tilt bed rest at all time. The exercise starts at 40% of VO2max for 5 minutes, followed by a series of 2-minute high- and low-intensity intervals for 20 minutes. 2-minute high-intensity intervals are at 65% VO2max, 70% VO2max, 80% VO2max, 80% VO2max, 70% VO2max and 65% VO2max. 2-minute low-intensity intervals are at 40% VO2max. 3 minutes at 40% of VO2max will end the exercise.
VO2max is measured for each volunteer in supine position.
Countermeasure AG-BikeBehavioural
60 days of strict head down tilt bed rest at all time. The exercise starts at 40% of VO2max for 5 minutes, followed by a series of 2-minute high- and low-intensity intervals for 20 minutes. 2-minute high-intensity intervals are at 65% VO2max, 70% VO2max, 80% VO2max, 80% VO2max, 70% VO2max and 65% VO2max. 2-minute low-intensity intervals are at 40% VO2max. 3 minutes at 40% of VO2max will end the exercise.
VO2max is measured for each volunteer in supine position.
The supine bike exercise is performed in a short arm centrifuge in rotation. Volunteers will start pedalling and the centrifuge will start at 0.15 Gz less than individual's threshold.
Every 4 minutes thereafter, the AG will be increased by 0.15 Gz, synchronized with the ramping up of cycle ergometer interval intensity. The AG will increase only up to 70 % of their tolerance level,.
It will then decrease by 0.15 Gz every 4 minutes, and until the 30-minute exercise is completed.
| Study group | Role | What they receive |
|---|---|---|
| Control Group | Experimental | Control group does not receive any countermeasure program during the head down tilt phase. Receives: Behavioral: Control Group |
| Artificial Gravity and Supine Bike | Experimental | The volunteers in this group receive countermeasure exercises during the head down tilt phase.
6 days over 7, they will perform a 30 minutes exercises on a supine bike (incremental steps) combined with artificial gravity generated with a short arm centrifuge. Receives: Behavioral: Countermeasure AG-Bike |
| Supine Bike | Experimental | The volunteers in this group receive countermeasure exercises during the head down tilt phase.
6 days over 7, they will perform a 30 minutes exercises on a supine bike (incremental steps). Receives: Behavioral: Countermeasure Supine Bike |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in orthostatic tolerance
Orthostatic tolerance will be assessed during a tilt test combined with Lower Body Negative Pressure test (LBNP test)
Measured: At baseline and first day of recovery
Changes in peak aerobic power (VO2max test)
Exercise capacity wil be assessed by graded cycling on sitting ergometer until exhaustion
Measured: At baseline and end of head down tilt phase at week 10
Changes in plasma volume
Plasma volume (L) will be assessed by the carbon monoxide-rebreathing method
Measured: At baseline and end of head down tilt phase at week 10
Changes in serum bone formation markers
Change in bone-specific Alkaline Phosphatase (bAP, µg/L) and procollagen type I N-terminal propeptide (P1NP, µg/L) will be assessed by chemiluminescence immunoassay
Measured: From baseline until the end of the volunteers' participation in the study at year 2
Change in serum bone resorption markers
Change in C-terminal cross-linked telopeptide of type I collagen (CTx, pmol/L) and N-terminal cross-linked telopeptide of type I collagen (NTX, pmol/L) will be assessed by chemiluminescence immunoassay.
Measured: From baseline until the end of the volunteers' participation in the study at year 2
Changes in Resting Metabolic Rate (RMR)
RMR will be measured by indirect calorimetry technique
Measured: At baseline and at recovery at week 12
Change in nitrogen balance
Nitrogen balance is a measure of nitrogen input minus nitrogen output. Nitrogen intake is calculated with a nutrition software. Protein oxidation measured in the 24-Hour urine collection estimates nitrogen output.
Measured: At baseline and at recovery at week 12
Change in muscle strength
Muscle strength will be assessed from single leg isometric maximal voluntary contraction on the knee extensors \& flexors, the plantarflexors and dorsiflexors. The Isometric Torque will be measured in Nm. The peak of the three maximal attempts will be recorded for strength measures
Measured: At baseline and at recovery at week 10
Change in fat and lean body mass measured by dual energy x-ray absorptiometry (DEXA)
Dual energy x-ray absorptiometry is a standard clinical technique to assess fat (g) and lean (g) body mass.
Measured: From baseline until the end of the volunteers' participation in the study at year 2
Change in walking balance
Functional mobility test (such as sit and walk, heel to toe steps with eyes closed and open) will assess walking balance
Measured: At baseline and at recovery at week 10
Changes in jump performance
Jump performance will be assessed on a platform and height of the jump will be evaluated
Measured: At baseline and at recovery at week 12
Change in standing balance
Standing balance will be assessed by posturography eyes open and eyes closed on a platform covered with 12-cm thick medium density foam
Measured: At baseline and at recovery at week 10
Changes in leg muscle volume and fat
MRI of the lower extremity will assess the degree of atrophy and changes in fat content in the musculature
Measured: At baseline and at recovery at week 10
Changes in bone density (by DEXA and High Resolution Peripheral Computed Tomography (HR-pQCT))
Bone density is measured at lumbar and hip level with DEXA and at tibia and radius level with HR-pQCT
Measured: From baseline until the end of the volunteers' participation in the study at year 2
Change in the optic nerve fibers thickness
Thickness of the optic nerve fibers will be measured by Optical Coherence Tomography (OCT)
Measured: At baseline and at recovery at week 12
Change in intraocular pressure (IOP)
IOP is measured with air tonometry
Measured: At baseline and at recovery at week 12
Change in visual acuity
Far and near visual acuity are tested uncorrected, or if applicable with own correction with digital acuity system
Measured: At baseline and at recovery at week 12
Change in visual field
Visual field measured by standard automated perimetry
Measured: At baseline and at recovery at week 12
Change in the anatomical characteristics of the eye (optical biometry)
Optical biometry measured by partial coherence interferometry
Measured: At baseline and at recovery at week 12
Change in the central corneal thickness
Central corneal thickness on a single point on the cornea measured by Ultrasonic pachymetry
Measured: At baseline and at recovery at week 12
Change in the retina by non-mydriatic fundus retinography
Non-mydriatic fundus retinography allows a fundus photography to be taken and thus a color image of the papilla, retinal vessels and macula
Measured: At baseline and at recovery at week 12
Change in the cornea topography
Cornea topography measured by corneal topography equipment (like Pentacam). The elevation topography allows the mapping of the anterior and posterior surface of the cornea.
Measured: At baseline and at recovery at week 12
Change in motion sickness susceptibility
Assessed by the Motion Sickness Susceptibility Questionnaire Short form (MSSQ-Short). MSSQ-Short scores possible range from minimum 0 to maximum 54, the maximum being unlikely. Higher scores means a higher motion sickness susceptibility
Measured: At baseline and at recovery at week 12
Change in fluid shift distribution towards the cardiac and cephalic region
The consequences of the fluid shift on the cardiac and cephalic area will be assessed by quantifying the right and left Jugular veins volumes (mL), as well as the left ventricle diastolic/systolic volumes (mL) by ultrasound.
Measured: At baseline and until year 1
Change in mood
Change in mood is assessed using the Profile of Mood States (POMS) questionnaire. POMS questionnaire gives 6 measures of mood:
Tension/anxiety, Depression, Anger/hostility Dynamism, Fatigue, Confusion A Total Mood Disturbance (TMD) score is calculated by summing the totals for the negative subscales (tension, depression, fatigue, confusion, anger) and then subtracting the totals for the positive subscale (vigor /esteem-related affect).
Measured: At baseline and until week 12
Change in affective states
Positive and Negative Schedule (PANAS) questionnaire will be used to assess the intensity of positive and negative affective states. PANAS self-report questionnaire consists of two 10-item scales to measure both positive and negative affects
Each item is rated on a five-point Likert Scale, ranging from 1 = Not at all to 5 = Extremely, to measure the extent to which the affect has been experienced in a specified time frame.
Positive affects: scores can range from 10 - 50 with higher scores representing higher levels of positive affect.
Negative affects: scores can range from 10 - 50 with higher scores representing higher levels of negative affect.
Measured: At baseline and until week 12
Change in sleep quality
Pittsburgh Sleep Dairy (PghSD) will be used to assess sleep perceived quality. The PghSD is an instrument with separate components to be completed at bedtime and wake time. The following parameters are registered or assessed:
Bedtime, wake time, sleep latency, wake after sleep onset, total sleep time, mode of awakening and ratings of sleep quality, mood, and alertness on wakening, as well as daytime information on naps, exercise, meals and caffeine, tobacco and medications use.
Measured: At baseline and until week 12
Change in psychological state: mental health
General Health Questionnaire-28 (GHQ-28) will be used to assess psychological well-being and capture distress
GHQ-28 gives an overall total score and 4 scores for 4 subscales:
Somatic symptoms, Anxiety/insomnia, Social dysfunction, Severe depression. Higher scores indicate higher levels of distress
Measured: At baseline and until week 12
Measurement of changes in subjective sleep quality
Changes in subjective sleep quality will be measured using the Karolinska sleepiness scale (KSS) two times per day (bed time) every week.
Measured: At baseline and until week 12
Secondary outcomes (4)
Change in vertebral bone marrow fat fraction.
This will be performed by using MR scanning sequences that specifically measure water and fat signals then calculate the respective content.
Measured: At baseline and until year 1
Changes in myokinins.
Mass spectrometry will be performed on proteins obtained from muscle biopsies, microdialysis and serum. The generated peptides will be analysed using high resolution mass shot-gun mass spectrometry.
Measured: At baseline and until week 12
Changes in brain structure
Both structural and functional brain changes associated with head-down bedrest will be examined by 3 Tesla MRI. Imaging sequence parameters will be selected to maximize sensitivity to effects of interest.
Measured: At baseline and until week 12
Change in pulse wave velocity in carotid and femoral arteries
Change in pulse wave velocity in carotid and femoral arteries will be assessed by non-invasive ultrasound measurements.
Measured: At baseline and until year 1
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Aug 2024
- Study start6 Feb 2023
- Primary completion20 Apr 2024
- Study completion6 Jun 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Simulated Microgravity by Head Down Tilt BedrestStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Volunteers are divided in three groups (8 volunteers each), one control group, one group with supine bike as countermeasure, one group with artificial gravity and supine bike as countermeasure
- Masking
- None (open label)
- Enrolment
- 24 participants (actual)
Sponsor and investigators
- Lead sponsor
- Centre National d'Etudes Spatiales
- Sponsor type
- Other government
- Collaborators
- European Space Agency, MEDES - IMPS
- Responsible party
- Sponsor
- Investigators
- Rebecca Billette de Villemeur, Principal investigator, MEDES - Institut de Médecine et Physiologie Spatiale
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06544213
- Sponsor's protocol ID
- 20-242
- Other IDs
- 2022-A02074-39
- Acronym
- BRACE
- Status last verified
- Jul 2026
- First submitted
- 25 Jul 2024
- Last updated
- 10 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized Controlled Study on 24 Healthy Male Volunteers Evaluating the Effects of Centrifugation and Exercise to Prevent the Deconditioning Induced by 60 Days of Head-down Bedrest Used as a Ground-based Model to Mimic Weightlessness.
- ClinicalTrials.gov ID
- NCT06544213
- Acronym / sponsor ID
- BRACE / 20-242
- Keywords
- Simulation of microgravity, Weightlessness, Artificial Gravity, Bedrest, Countermeasure
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 24 participants (actual)
- Lead sponsor
- Centre National d'Etudes SpatialesOther government
- Collaborators
- European Space Agency, MEDES - IMPS
- Study start
- 6 Feb 2023 (actual)
- Primary completion
- 20 Apr 2024 (actual)
- Study completion
- 6 Jun 2026 (actual)
- First posted
- 9 Aug 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The objective of this study is to investigate whether a cycling exercise coupled with artificial gravity via a short-arm human centrifuge helps to prevent and / or reduce the deleterious effects induced by 60 days of anti-orthostatic bedrest.
The secondary objective is to investigate whether the combination of a supine cycling exercise with artificial gravity is more effective than the same supine cycling exercise alone in preventing or reducing the effects of head-down bedrest.
During a randomized, 60 day bed rest study, in 24 healthy male adults, the two following aims will be undertaken:
- Fourteen scientific protocols will assess the changes in the cardiovascular, metabolic, musculoskeletal, neuro-sensorial, haematological, and immunological systems.
- In the above-mentioned systems, the comparative potential beneficial effects of the two countermeasure protocols will also be investigated by the scientific protocols and bedrest standard measurements (BSM).
Detailed description
Space flights have shown the possibilities and limitations of human adaptation to space. For the last 60 years, results have shown that the space environment and microgravity in particular, cause changes that may affect the performance of astronauts. These physiological changes are now better known: prolonged exposure to weightlessness can lead to significant loss of bone and muscle mass, strength, cardiovascular and sensory-motor deconditioning, immune, hormonal and metabolic changes .
Moreover, recently a new suite of physiological adaptations and consequences of space flight has been acknowledged. Indeed, after long flights, some astronauts present persistent ophthalmologic changes, mostly a hyperopic shift, an increase in optic nerve sheath diameter and occasionally a papillary oedema now defined by National Aeronautics and Space Administration (NASA) as Spaceflight-Associated Neuro-ocular Syndrome (SANS). Some of these vision changes remain unresolved for years post-flight. This phenomenon has most likely existed since the beginning of human space flight but is just recently being recognized as a major consequence of adaptation to microgravity.
Overall, spaceflight induces physiological multi-system deconditioning which may impact astronauts' efficiency and create difficulties upon their return to normal gravity. Understanding the underlying mechanisms of these processes and developing efficient countermeasures to prevent, limit or reverse this deconditioning remain important challenges and major priorities for manned space programs.
The space agencies are actively engaged in studying the physiological adaptation to space environment through studies on board the International Space Station (ISS) but also on the ground. Indeed, considering the limited number of flight opportunities, the difficulties related to the performance of in-flight experiments (operational constraints for astronauts, limited capabilities of in-flight biomedical devices), ground-based experiments simulating the effects of weightlessness are used to better understand the mechanisms of physiological adaptation, design and validate the countermeasures.
Different methods are used to simulate microgravity on Earth. However, two approaches, -6° head-down bed rest (HDBR) and dry immersion (DI) have provided possibilities for long-term exposures with findings closest to those seen with a weightless state. They produce changes in body composition (including body fluid redistribution), cardiovascular and skeletal muscle characteristics that resemble the effects of microgravity. One of the advantages of the HDBR model is that it has now been used in a great number of studies internationally, and its effects have long been described and compared with those of microgravity and spaceflight. Long-term bedrest is the gold-standard method for studying the effects of weightlessness and to test countermeasures.
The HDBR, as the name implies, implicates a long (from several weeks to a year) stay in the supine position, the head tilted down by -6° from the horizontal plane. HDBR is the most frequently used ground-based simulation for gravitational unloading of the human body in western countries.
During human space missions, the current most effective countermeasure is physical exercise. However, it is both time-consuming and not completely satisfactory. One of the solutions for this is to combine physical exercise with artificial gravity, with the use of a short-arm human centrifuge (SAHC). This study proposes to test the effectiveness of a countermeasure protocol combining Artificial Gravity (AG) with a cycling exercise, and to compare it with only a cycling exercise, and with a complete lack of physical exercise.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- Volunteers are divided in three groups (8 volunteers each), one control group, one group with supine bike as countermeasure, one group with artificial gravity and supine bike as countermeasure
| Arm | Type | Receives |
|---|---|---|
| Control Group | Experimental | Behavioral: Control GroupControl group does not receive any countermeasure program during the head down tilt phase. |
| Artificial Gravity and Supine Bike | Experimental | Behavioral: Countermeasure AG-BikeThe volunteers in this group receive countermeasure exercises during the head down tilt phase. 6 days over 7, they will perform a 30 minutes exercises on a supine bike (incremental steps) combined with artificial gravity generated with a short arm centrifuge. |
| Supine Bike | Experimental | Behavioral: Countermeasure Supine BikeThe volunteers in this group receive countermeasure exercises during the head down tilt phase. 6 days over 7, they will perform a 30 minutes exercises on a supine bike (incremental steps). |
Who may qualify
- Ages
- 20 to 45 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (12 listed)
- Healthy male volunteer (see below the description of medical tests and laboratory analysis performed at the selection visit)
- Aged 20 to 45 years
- No overweight nor excessive thinness with BMI (weight kg/ height m2) between 20 and 27 kg/m2
- Height between 158 and 190 cm
- Certified as healthy by a comprehensive clinical assessment (detailed medical history and complete physical examination): in particular, free from any chronic disease or any acute infectious disease or cardiovascular, neurological, of the ear, nose, throat (especially orthostatic hypotension and vestibular disorders), orthopaedic or musculoskeletal disorders
Key exclusion criteria (38 listed)
- Any history or presence of clinically relevant cardiovascular, neurological or ear, nose, throat disease, any chronic disease; any acute infectious disease. Particularly:
- Symptomatic orthostatic hypotension whatever the decrease in blood pressure, or asymptomatic postural hypotension defined by a decrease in systolic blood pressure equal to or greater than 20 mmHg within 3 minutes when changing from the supine to the standing position,
- Cardiac rhythm disorders,
- Hypertension,
- Chronic back pains,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Control Group60 days of strict head down tilt bed rest at all time. No countermeasure program is performed. | Behavioural | Control Group |
| Countermeasure Supine Bike60 days of strict head down tilt bed rest at all time. The exercise starts at 40% of VO2max for 5 minutes, followed by a series of 2-minute high- and low-intensity intervals for 20 minutes. 2-minute high-intensity intervals are at 65% VO2max, 70% VO2max, 80% VO2max, 80% VO2max, 70% VO2max and 65% VO2max. 2-minute low-intensity intervals are at 40% VO2max. 3 minutes at 40% of VO2max will end the exercise. VO2max is measured for each volunteer in supine position. | Behavioural | Supine Bike |
| Countermeasure AG-Bike60 days of strict head down tilt bed rest at all time. The exercise starts at 40% of VO2max for 5 minutes, followed by a series of 2-minute high- and low-intensity intervals for 20 minutes. 2-minute high-intensity intervals are at 65% VO2max, 70% VO2max, 80% VO2max, 80% VO2max, 70% VO2max and 65% VO2max. 2-minute low-intensity intervals are at 40% VO2max. 3 minutes at 40% of VO2max will end the exercise. VO2max is measured for each volunteer in supine position. The supine bike exercise is performed in a short arm centrifuge in rotation. Volunteers will start pedalling and the centrifuge will start at 0.15 Gz less than individual's threshold. Every 4 minutes thereafter, the AG will be increased by 0.15 Gz, synchronized with the ramping up of cycle ergometer interval intensity. The AG will increase only up to 70 % of their tolerance level,. It will then decrease by 0.15 Gz every 4 minutes, and until the 30-minute exercise is completed. | Behavioural | Artificial Gravity and Supine Bike |
Primary outcome
Changes in orthostatic tolerance
Time frame: At baseline and first day of recovery
Orthostatic tolerance will be assessed during a tilt test combined with Lower Body Negative Pressure test (LBNP test)
Changes in peak aerobic power (VO2max test)
Time frame: At baseline and end of head down tilt phase at week 10
Exercise capacity wil be assessed by graded cycling on sitting ergometer until exhaustion
Changes in plasma volume
Time frame: At baseline and end of head down tilt phase at week 10
Plasma volume (L) will be assessed by the carbon monoxide-rebreathing method
Changes in serum bone formation markers
Time frame: From baseline until the end of the volunteers' participation in the study at year 2
Change in bone-specific Alkaline Phosphatase (bAP, µg/L) and procollagen type I N-terminal propeptide (P1NP, µg/L) will be assessed by chemiluminescence immunoassay
Change in serum bone resorption markers
Time frame: From baseline until the end of the volunteers' participation in the study at year 2
Change in C-terminal cross-linked telopeptide of type I collagen (CTx, pmol/L) and N-terminal cross-linked telopeptide of type I collagen (NTX, pmol/L) will be assessed by chemiluminescence immunoassay.
Changes in Resting Metabolic Rate (RMR)
Time frame: At baseline and at recovery at week 12
RMR will be measured by indirect calorimetry technique
Change in nitrogen balance
Time frame: At baseline and at recovery at week 12
Nitrogen balance is a measure of nitrogen input minus nitrogen output. Nitrogen intake is calculated with a nutrition software. Protein oxidation measured in the 24-Hour urine collection estimates nitrogen output.
Change in muscle strength
Time frame: At baseline and at recovery at week 10
Muscle strength will be assessed from single leg isometric maximal voluntary contraction on the knee extensors \& flexors, the plantarflexors and dorsiflexors. The Isometric Torque will be measured in Nm. The peak of the three maximal attempts will be recorded for strength measures
Change in fat and lean body mass measured by dual energy x-ray absorptiometry (DEXA)
Time frame: From baseline until the end of the volunteers' participation in the study at year 2
Dual energy x-ray absorptiometry is a standard clinical technique to assess fat (g) and lean (g) body mass.
Change in walking balance
Time frame: At baseline and at recovery at week 10
Functional mobility test (such as sit and walk, heel to toe steps with eyes closed and open) will assess walking balance
Changes in jump performance
Time frame: At baseline and at recovery at week 12
Jump performance will be assessed on a platform and height of the jump will be evaluated
Change in standing balance
Time frame: At baseline and at recovery at week 10
Standing balance will be assessed by posturography eyes open and eyes closed on a platform covered with 12-cm thick medium density foam
Changes in leg muscle volume and fat
Time frame: At baseline and at recovery at week 10
MRI of the lower extremity will assess the degree of atrophy and changes in fat content in the musculature
Changes in bone density (by DEXA and High Resolution Peripheral Computed Tomography (HR-pQCT))
Time frame: From baseline until the end of the volunteers' participation in the study at year 2
Bone density is measured at lumbar and hip level with DEXA and at tibia and radius level with HR-pQCT
Change in the optic nerve fibers thickness
Time frame: At baseline and at recovery at week 12
Thickness of the optic nerve fibers will be measured by Optical Coherence Tomography (OCT)
Change in intraocular pressure (IOP)
Time frame: At baseline and at recovery at week 12
IOP is measured with air tonometry
Change in visual acuity
Time frame: At baseline and at recovery at week 12
Far and near visual acuity are tested uncorrected, or if applicable with own correction with digital acuity system
Change in visual field
Time frame: At baseline and at recovery at week 12
Visual field measured by standard automated perimetry
Change in the anatomical characteristics of the eye (optical biometry)
Time frame: At baseline and at recovery at week 12
Optical biometry measured by partial coherence interferometry
Change in the central corneal thickness
Time frame: At baseline and at recovery at week 12
Central corneal thickness on a single point on the cornea measured by Ultrasonic pachymetry
Change in the retina by non-mydriatic fundus retinography
Time frame: At baseline and at recovery at week 12
Non-mydriatic fundus retinography allows a fundus photography to be taken and thus a color image of the papilla, retinal vessels and macula
Change in the cornea topography
Time frame: At baseline and at recovery at week 12
Cornea topography measured by corneal topography equipment (like Pentacam). The elevation topography allows the mapping of the anterior and posterior surface of the cornea.
Change in motion sickness susceptibility
Time frame: At baseline and at recovery at week 12
Assessed by the Motion Sickness Susceptibility Questionnaire Short form (MSSQ-Short). MSSQ-Short scores possible range from minimum 0 to maximum 54, the maximum being unlikely. Higher scores means a higher motion sickness susceptibility
Change in fluid shift distribution towards the cardiac and cephalic region
Time frame: At baseline and until year 1
The consequences of the fluid shift on the cardiac and cephalic area will be assessed by quantifying the right and left Jugular veins volumes (mL), as well as the left ventricle diastolic/systolic volumes (mL) by ultrasound.
Change in mood
Time frame: At baseline and until week 12
Change in mood is assessed using the Profile of Mood States (POMS) questionnaire. POMS questionnaire gives 6 measures of mood: Tension/anxiety, Depression, Anger/hostility Dynamism, Fatigue, Confusion A Total Mood Disturbance (TMD) score is calculated by summing the totals for the negative subscales (tension, depression, fatigue, confusion, anger) and then subtracting the totals for the positive subscale (vigor /esteem-related affect).
Change in affective states
Time frame: At baseline and until week 12
Positive and Negative Schedule (PANAS) questionnaire will be used to assess the intensity of positive and negative affective states. PANAS self-report questionnaire consists of two 10-item scales to measure both positive and negative affects Each item is rated on a five-point Likert Scale, ranging from 1 = Not at all to 5 = Extremely, to measure the extent to which the affect has been experienced in a specified time frame. Positive affects: scores can range from 10 - 50 with higher scores representing higher levels of positive affect. Negative affects: scores can range from 10 - 50 with higher scores representing higher levels of negative affect.
Change in sleep quality
Time frame: At baseline and until week 12
Pittsburgh Sleep Dairy (PghSD) will be used to assess sleep perceived quality. The PghSD is an instrument with separate components to be completed at bedtime and wake time. The following parameters are registered or assessed: Bedtime, wake time, sleep latency, wake after sleep onset, total sleep time, mode of awakening and ratings of sleep quality, mood, and alertness on wakening, as well as daytime information on naps, exercise, meals and caffeine, tobacco and medications use.
Change in psychological state: mental health
Time frame: At baseline and until week 12
General Health Questionnaire-28 (GHQ-28) will be used to assess psychological well-being and capture distress GHQ-28 gives an overall total score and 4 scores for 4 subscales: Somatic symptoms, Anxiety/insomnia, Social dysfunction, Severe depression. Higher scores indicate higher levels of distress
Measurement of changes in subjective sleep quality
Time frame: At baseline and until week 12
Changes in subjective sleep quality will be measured using the Karolinska sleepiness scale (KSS) two times per day (bed time) every week.
4 secondary outcomes
Change in vertebral bone marrow fat fraction.
Time frame: At baseline and until year 1
Changes in myokinins.
Time frame: At baseline and until week 12
Changes in brain structure
Time frame: At baseline and until week 12
Change in pulse wave velocity in carotid and femoral arteries
Time frame: At baseline and until year 1
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Jul 2026.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Rebecca Billette de Villemeur principal investigator
MEDES - Institut de Médecine et Physiologie Spatiale
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Countermeasure Supine Bike and Countermeasure AG-Bike in people with Simulated Microgravity by Head Down Tilt Bedrest and Weightlessness, run by Centre National d'Etudes Spatiales at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 12 inclusion and 38 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 10 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in orthostatic tolerance (time frame: At baseline and first day of recovery). The study lists 29 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jul 2026.