Actively Recruiting
Use of Velocity Monitoring to Prescribe Flywheel-based Inertial Training Workloads for Exercise During Space Flight Simulation
Led by Lance Bollinger · Updated on 2025-10-24
16
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
L
Lance Bollinger
Lead Sponsor
U
University of Louisville
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating how flywheel-based inertial training (FIT), applied using velocity-based training (VBT) and high-intensity interval training (HIIT), impacts physical decline caused by disuse. This includes examining muscle strength loss, aerobic capacity reduction, and balance problems. The study focuses on healthy adults aged 35 to 45 who will experience 30 days of unilateral lower limb suspension (ULLS) to simulate muscle disuse. Participants will wear a specially modified shoe and use crutches to unload one leg during daily activities. They will be randomly assigned to either a control group with no exercise or an exercise group performing FIT leg press and upright squats three times weekly. The FIT exercises use a flywheel device adjusted for specific movement speeds and include resistance training and high-intensity intervals. The study duration for the suspension and exercise intervention is 30 days. Throughout the study, participants will undergo multiple assessments before, during, and after the intervention. These include body composition measurements, balance testing with force platforms, aerobic capacity tests using cycling with gas exchange monitoring, muscle imaging with diffusion tensor imaging, and muscle strength evaluations. Researchers will measure muscle activation, twitch properties, motor unit behavior, muscle size, and physiological changes at baseline, day 13, and day 30. Secondary outcomes include heart rate, blood pressure, and postural sway. The entire participation lasts about one month with repeated testing sessions.
CONDITIONS
Brief Title
FIT Exercise in 30d of ULLS-induced Muscle Disuse
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Regularly engaging in aerobic exercise (> 150 minutes per week) and resistance exercise (at least once weekly) for the past 12 months
- Education level of bachelor's degree or higher in any field
- Age between 35 and 45 years
- Healthy, physically active individuals
You will not qualify if you...
- Female waist circumference less than 55 cm or greater than 90 cm
- Male waist circumference less than 75 cm or greater than 100 cm
- Body mass index less than 18.5 or greater than 29.9
- Shoe size less than 25 cm or greater than 29 cm
- Not regularly engaging in exercise during the past 12 months
- Tobacco use within the past 6 months
- Blood clotting disorders
- Heart arrhythmia
- Implanted devices affected by electrical impulses or magnetic fields (e.g., pacemaker, defibrillator, cochlear implant)
- Diagnosed cardiovascular, pulmonary, renal, or metabolic disease
- Pregnancy within the past 6 months
- Oral contraceptive use within the past 3 months
- High resting blood pressure (systolic >140 or diastolic >90)
- Current or previous gender-affirming therapy (hormone or surgical)
- Low back or leg injury in the past 6 months
- Use of medication to assist with sleep
- Muscle, bone, or joint injuries limiting physical activity in the past 6 months
- Neurological disorders affecting balance such as multiple sclerosis or Parkinson's disease
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
2 testing sessions prior to the intervention
Duration - 30 days
Participants undergo 30 days of Unilateral Lower Limb Suspension (ULLS) during daily living activities, ambulating with a specially modified shoe and forearm crutches. Participants assigned to the exercise group perform Flywheel-based Inertial Training (FIT) leg press exercises three times per week, including high-intensity resistance and aerobic training.
1 testing session at day 13 during the intervention
Duration - Immediately following the 30-day intervention
Participants complete two testing sessions at the end of the study to assess muscle function, balance, aerobic capacity, and body composition after the intervention period.
2 testing sessions post-intervention
Trial Site Locations
Total: 1 location
1
University of Kentucky
Lexington, Kentucky, United States, 40506
Actively Recruiting
Research Team
L
Lance Bollinger, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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