Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
48 participants
INTERVENTIONAL
2023-04-01
2024-01-31
Brief Summary
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Participants will complete an inclusion questionnaire and, if eligible, be invited to visit the exercise laboratory 4-5-hours. We will collect questionnaire data and body measurements before participants undertake exercise on a treadmill. Biological samples (blood from adults only and saliva from everyone) will be collected at three time points (before, right after and one hour after exercise).
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Detailed Description
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The in-person part of the study will take place at the University Of East London SportsDock (4-6 University Way, London E16 2RD) and last 4-5 hours. No breakfast or coffee/tea should be consumed on the day of the visit, but the investigators will offer the participants breakfast. The participants will also need to not have had any alcohol, recreational drugs, or exercise for 24 hours.
On the day, the investigators will first measure their resting heart rate and blood pressure, collect body measurements (weight, height, waist circumference, hip circumference), and measure their body composition. The last thing the investigators will do before breakfast is to collect some samples. The investigators will collect two separate saliva samples using synthetic cotton swabs. After this, the investigators will collect a blood sample by venepuncture ("needle prick") from the adults only. This first part of the study will take 45-60 minutes.
Along with breakfast, the investigators will ask the participants to consume a dose of deuterium-labelled water: an odourless, tasteless, and safe water that will allow us to measure their total body water content. The investigators will also ask the participants to complete two short questionnaires assessing their mood, appetite, feeling of tiredness as well as verbal learning. This part will take approximately 30 minutes.
The researcher will then help the participants familiarise with the treadmill and associated equipment. The participants will wear a chest strap under their clothes and a special face mask which will be held in place by a head strap. These will measure their heart rate and everything the participants breathe in and out throughout the exercise challenge, respectively. The treadmill will start slowly to help the participants warm up and familiarise with the feeling of walking on it. After 2 minutes, the exercise challenge will begin. This will last for approximately 20 minutes, during which the treadmill will increase the speed and/or the incline every 2 minutes. It will feel like the participants are walking more briskly and more uphill, but it will not be too fast. The researcher will encourage the participants to complete the exercise challenge, as this will get the best response from their metabolism and give us the most accurate results. The participants will be able to stop the treadmill if the participants feel too exhausted to continue, feel faint or develop chest pain.
Right after the participants complete the exercise challenge, the investigators will collect a saliva sample using a synthetic cotton swab and a blood sample by venepuncture (adults only). The investigators will then ask the participants to complete the same two short questionnaires as before. This part will take approximately 30 minutes.
Finally, the researcher will allow the participants to relax and rest for about an hour. The investigators will then collect the last saliva samples using synthetic cotton swabs and blood samples by venepuncture (adults only). The participants will then complete the last iteration of the two short questionnaires.
Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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Single arm
Study participants are asked to undertake the Cornell treadmill exercise protocol which they complete to voluntary exhaustion.
Cornell treadmill exercise protocol
Study participants are asked to undertake the Cornell treadmill exercise protocol which they complete to voluntary exhaustion.
Interventions
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Cornell treadmill exercise protocol
Study participants are asked to undertake the Cornell treadmill exercise protocol which they complete to voluntary exhaustion.
Eligibility Criteria
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Inclusion Criteria
2. Considered healthy without a disease, disability or other condition that would impair participation in physical activity.
3. Considered active.
4. A body mass index within the ranges of 19 to 24.5 (adults) or the 2nd and 99th percentile (children)
Exclusion Criteria
2. Having a disease, disability or other condition that would impair participation in physical activity.
3. Having an implanted cardiac pacemaker, defibrillator, or other electronic medical devices.
4. Receiving prescription medication one or more days every week over the past 3 months (some medications are permitted).
5. Related by blood to another participant.
6. Not willing at the time of recruitment to undergo blood sampling (adults only).
7. Pregnancy/breastfeeding (adults only).
8. Being a professional athlete.
9. Not being physically active.
10. Being a shift worker (night shift work for three or more days per week on more than two occasions in the six months before the visit day; adults only).
11. Recent weight loss of more than 5% of weight in the last 6 months.
12. Having a body mass index outside the range of 19 to 24.5 (adults) or outside the 2nd and 99th percentile (children)
13. Smoking/vaping.
14. Alcohol intake above a UK National Health Service (NHS) questionnaire cut-off.
15. Regular use of recreational drugs.
16. Not having reached menopause (for women aged 53-57 only).
8 Years
57 Years
ALL
Yes
Sponsors
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University of East London
OTHER
Imperial College London
OTHER
University College, London
OTHER
Responsible Party
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Principal Investigators
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Jonathan Wells, Professor
Role: PRINCIPAL_INVESTIGATOR
University College, London
Locations
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University of East London SportsDock
London, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Provided Documents
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Document Type: Informed Consent Form
Other Identifiers
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Metabex
Identifier Type: -
Identifier Source: org_study_id
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