The primary objective is to show that energy expenditure of the body, during moderate physical activity on a bike ergometer, can become higher in response to high altitude simulation. The secondary objetive is to show that an increase in energy…
ID
Source
Brief title
Condition
- Other condition
Synonym
Health condition
overweight (25 < BMI < 30)
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
As parameter of energy expenditure whole body oxygen consumption is measured
via indirect calorimetry (ventilated hood).
A work load of 85 Watt on a bike ergometer (the maximum in this study) requires
at sea level an energy expenditure of 20.4 kJ/min.
We expect that the same work load under high altitude simulation requires an
energy expenditure of 28.6 kJ/min, an increase of about 40%.
In other words a work load of 85 Watt under high altitude simulation is
associated with an energy expenditure for which under sea level conditions a
work load of 115 Watt has to be applied.
Secondary outcome
The CO2 production of the subjects is also measured via the ventilated hood
system. In combination with the oxygen consumption the Respiratory Quotient (RQ
= CO2/O2) can be determined. Changes in RQ are indicative for for changes in
substrate use. During the exercise protocols at regular time intervals 10 ul
blood samples are taken from the middle finger to detect changes in glucose and
lactate levels in peripheral blood. During the exercise protocols the lactate
level should be higher compared to rest and may increase slightly.
The physiological condition of the subjects is continuously monitored via
oxygen saturation of the blood (SpO2), the heart rate (HR) and a RPE (Rate of
Perceived Exertion) questionaire. The protcol is stopped when the subject wants
to do so and when the pre-determined endpoint values are reached; SpO2 < 90% en
HR > 80% HRmax.
Background summary
An unintended loss of body weight is not uncommon for mountaineers and for
people otherwise exposed to high altitude conditions (thin air) for a longer
period of time. COPD patients may experience similar effects because of their
respiratory problems. The nature of the weight loss is not always clear and is
supposed to be multifactorial. A reduction in body weight can be caused by a
loss of body water, body fat or lean body mass (protein). The size of the
weight loss seems to be related to the level and the duration of the high
altitude exposure, to the level of physical activity at altitude as well as to
the individual tolerance to high altitude conditions. Dehydration, reduced
appetite, a change in metabolic substrates and an increase in energy
expenditure have been suggested as potential mechanisms for weight loss under
high altitude conditions. The evidence for high altitude weight loss suggests
that exercise programmes for weight management could benefit from high altitude
simulation at sea level. An innovative approach of exercise programmes that
make use of high altitude simulation to increase energy expenditure provides in
our view the best perspective voor weight management. An acute increase in
energy expenditure, in response to high altitude simulation, has to be expected
when lactate, produced as residual product of anaerobic glycolysis,is cleared
by gluconeogenesis. It is well known that energy expenditure of the body
increases upon an increase in the level of gluconeogenesis.
Study objective
The primary objective is to show that energy expenditure of the body, during
moderate physical activity on a bike ergometer, can become higher in response
to high altitude simulation. The secondary objetive is to show that an increase
in energy expenditure can be linked to the clearance of lactate produced under
high altitude simulation as by product of as anaerobic glycolyis.
Study design
The study has a 'Randomised controlled single blind cross-over design'
Intervention
The study consists of a exercise protocol of 30 min. This exercise protocol is
executed twice, once under sea level conditions and once under high altitude
simulation (2000 m). For each individual the level of exercise is predetermined
by means of a LSSH (Lactate steady State - Hypoxia) screening protocol.
Study burden and risks
In order to participate in the study subjects have to fill in a questionairre
and will be subjected to a sport medical screening (a.o. ECG at max work load,
long function test). Based on this information obtained the sports physician
decides about in- or exclusion of the subjects. A LSSH (Lactate Steady State -
Hypoxia) screening is used to determine the highest word load (stages of 15
Watt) under which the subject is able to maintain a constant lactate level
under high altitude simulation. The exercise protocols will be performed under
sea level conditions and under high altitude simulation condition at a work
load 3 stages (= 45 Watt) lower. During the exercise protocols oxygen
consumption will be measured by indirect calorimetry (ventilated hood). During
the LSSH screening and the exercise protocols subjects have to behave s quite
as possible (no talking etc). On the morning of the sport medical screening,
the LSSH screening and the exercise sessions subjects have to come to the test
facilcity (HAN - SENECA) in an overnight fasting condition. During the LSSH
screening and the exercise session at max 12 small blood samples are taken from
the middle finger. At certain time intervals subjects are asked about their
'Rate of Perceived Exertion' (RPE).
Verlengde Groenestraat 75
6525 EJ Nijmegen
NL
Verlengde Groenestraat 75
6525 EJ Nijmegen
NL
Listed location countries
Age
Inclusion criteria
Women
Self reported healthy
20 - 40 years
25 < BMI < 30
Non - smoking
Activity level < Dutch 'Fitnorm'
Exclusion criteria
Extreme sensitive to hypoxia (oxygen saturation < 90 % at pO2 = 129 mm Hg)
• Anaemia (Hb < 7.5 mmol/L, Hc < 41%)
• Diabetes (fasting plasma glucose > 5.8 mmol/L and/or glucosuria)
• Following weight-reduction programme or medically prescribed diet
• Weight change > 2 kg during the last 2 months
• Medication that may influence energy metabolism, weight or food intake
• Gastrointestinal disorders (blood in stool, constipation and diarrhoea)
• History of medical or surgical events that may affect the study outcome
• Blood donation in the last month before the study or during the study
• Abnormal ECG or impaired lung function
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL29211.091.09 |