Sleep Disturbance Clinical Trial
Official title:
The Effects of Whole Body Unloading on Physiological Function
This study is a collaboration between the Centre of Human & Aerospace Physiological Sciences (CHAPS) and the Sleep and Brain Plasticity Centre (Department of Neuroimaging) at King's College London and the Sleep Disorders Centre at Guy's Hospital.The main purpose of the study is to evaluate the effects of a 7 day unloading period (simulating micro gravity) on muscle mass using three independent methods; two scanning techniques (magnetic resonance imaging (MRI) and dual x-ray absorptiometry (DXA)) and one that involves swallowing a capsule that contains a harmless chemical called creatine (D3-Creatine (D3-cr)) and then measuring its concentration in urine. In order to induce muscle loss, participants will be required to lie flat on their back on a water bed filled with water and salt (called hyper-buoyancy flotation (HBF)). As this situation is similar to that experienced in space, the investigators will also measure the effect of HBF on sleep, brain and physiological function - all things known to change in astronauts. Sixteen male subjects (18-40 yrs) will be recruited to participate in the study that will require physiological testing before, during and following both 7 days of normal conditions and 7 days of HBF bed-rest. Each subject will be exposed to the same conditions and assessments over the study period. As some loss of muscle is expected, participants will be offered an exercise rehabilitation programme upon completion of HBF with self-monitored and/or guided sessions based on those provided by the Space Medicine Office of the European Space Agency to returning astronauts.
The rapid loss of skeletal muscle occurs in extreme physiological conditions, most notably
within intensive care, hypoxia and during spaceflight. The cause of this accelerated loss is
unknown; however, interventions aiming to slow the decline may have profound effects on
quality of life post-surgery and, in space expedition terms, the ability to complete mission
critical tasks. In addition, the current methodologies available to measure total skeletal
muscle mass have limitations, lack accuracy (anthropometry and Bioelectrical Impedance
Analysis (BIA)) or are immobile and costly (dual x-ray absorptiometry (DXA) and magnetic
resonance imaging (MRI)).
The primary aim of this study is to investigate whole body skeletal muscle loss induced
through 7 consecutive days of whole-body immobilisation using three independent methods; dual
x-ray absorptiometry (DXA), magnetic resonance imaging (MRI) and D3-Creatine dilution
(D3-cr). A number of secondary aims are also targeted, which have the shared objective to
measure the impact of 7-days of immobilisation on HBF; 1. Muscular, neuromuscular and
cardiovascular adaptation; 2. Neurophysiology, sleep architecture and cognition; 3. A range
of spaceflight specific measures, aiming to characterise the intervention proposed within
this study (hyper-buoyancy flotation (HBF) bed rest) as an alternative ground-based analogue
to observe the physiological response to microgravity.
The muscular, neuromuscular and cardiovascular research is performed by King's College London
Centre of Human & Aerospace Physiological Sciences (KCL CHAPs) and ranges from measurement of
whole-body change, to cellular adaptation. Total skeletal muscle mass will be measured using
DXA, MRI and D3-cr as well as the cross-sectional area of a single muscle group (quadriceps)
using ultrasound. A biopsy will be taken from the same muscle group (quadriceps) in order to
investigate changes in muscle protein synthesis (MPS), myofibre size, force and protein: DNA
ratio. Muscle performance will also be measured, from whole-body power output using a
countermovement jump, to force expressed by the trunk, quadriceps, calf and handgrip. Muscle
tone will be measured in three flexor and three extensor muscles in the calf, forearm and
lower back. The plantarflexion muscles in the calf will be further assessed, with ankle
proprioception, maximal strength and surface EMG of the medial gastrocnemius measured. Blood
samples will be taken in order to distinguish changes in immunity and bone markers. The
subject's height will be measured and intervertebral disc morphology distinguished using
ultrasound and MRI.
The neuromuscular and muscle performance measurements will be obtained concurrently.
Electrical activity produced by the skeletal muscles will be recorded and evaluated using
electromyography (EMG). Prior to the force expression of the quadriceps being tested, pads
will also be positioned for the muscle to be electrically stimulated and for a maximal
involuntary force to be measured. Lastly, a cycle ergometer assessment will be undertaken,
where power is ramped gradually and maximal aerobic utilisation (VO2max) determined.
The neurophysiology, sleep architecture and cognition investigation will be in collaboration
with the Sleep and Brain Plasticity Centre (Department of Neuroimaging, IoPPN) and the Sleep
Disorders Centre at Guy's Hospital. This study will look at any ensuing changes in sleep
architecture and neurophysiology. Any associated cognitive or brain structural changes, which
may be induced through 1 week of whole-body immobilisation, will also be investigated.
The procedures outlined are designed to assess known physiological adaptations occurring as a
consequence of a micro-gravity environment, and therefore prove useful comparative tools from
which the HBF model can be evaluated.
Sixteen male subjects (18-40 yrs) will be recruited to undertake test procedures pre- and
post- a 7-day control period, where they will continue their habitual activities and be
provided with their total (controlled) calorie intake, and pre- and post- a 7-day unloading
period, where subjects will be required to remain on a hyper-buoyancy flotation (HBF) bed.
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