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Healthy Subjects (HS)ExHypNCT07671638

Methodological Study of Exercise and Hypoxic Conditions in Healthy Subjects

A study testing Exercise and hypoxia in people with Healthy Subjects (HS) and Exercise, run by University Hospital, Grenoble at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

The aim of this protocol is to assess physiological responses during various physical exercise protocols (whole-body exercise such as cycling or treadmill running, or localised exercise such as knee extension) and during inhalation of a gas mixtures with various oxygen contents (similar to exposure at high altitude). Read more about this study

Who is it for?
Ages 18 to 55 yearsHealthy volunteers can take part
Conditions the study is for
Healthy Subjects (HS), Exercise, Hypoxia
What is being tested?
Exercise and hypoxia
Could I receive a placebo?
No, everyone receives an active treatment
How many people
305 participants
Where
1 siteFrance
Study dates
19 Oct 2026to 31 Mar 2032
Phase
Interventional

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 18 to 55 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Healthy male or female volunteers
  • Aged 18-55
  • Body Mass Index <30 kg/m²
  • Participants covered by a social security scheme
  • Participants capable of signing an informed consent form
  • Negative pregnancy test and highly effective contraception for women of childbearing age

Who cannot join

  • Cardiorespiratory, metabolic and neurological disorders, or other conditions assessed during the inclusion consultation that may affect physiological responses to exercise or hypoxia
  • Pharmacological treatment taken during the study, other than oral or implantable contraceptive medication for female volunteers of childbearing age

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

France1 site, 1 recruiting
  • CReSI (centre de recherche en santé intégrée)

    La Tronche, 38700

    Samuel VERGES, +33456589900, SVerges@chu-grenoble.fr

    Recruiting

Other trials in France

About this study

The aim of this protocol is to assess physiological responses during various physical exercise protocols (whole-body exercise such as cycling or treadmill running, or localised exercise such as knee extension) and during inhalation of a gas mixtures with various oxygen contents (similar to exposure at high altitude).

Being tested
Exercise and hypoxia
Medical subject headings
Motor Activity, Hypoxia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Exercise and hypoxiaCombination product

    Subjects will perform an exercise test while inhaling a hypoxic gas mixture

Study groups in NCT07671638
Study groupRoleWhat they receive
Exercise and hypoxiaExperimentalExercise test performed while inhaling a gas mixture
Receives: Combination Product: Exercise and hypoxia

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Muscle oxygenation

    Measured by NIRS in % saturation

    Measured: During 5 minutes before starting the exercise test, continuously during the exercise test and during 10 minutes immediatly after the end of the exercise test

Secondary outcomes (3)
  1. Gas exchange

    Oxygen consumption and cardon dioxide production measured at the mouth, measured in ml/min

    Measured: During 5 minutes before starting the exercise test, continuously during the exercise test and during 10 minutes immediatly after the end of the exercise test

  2. Heart rate

    Measured by ECG in bpm

    Measured: During 5 minutes before starting the exercise test, continuously during the exercise test and during 10 minutes immediatly after the end of the exercise test

  3. Limb blood flow

    Measured by Doppler ultrasound in ml/min

    Measured: During 5 minutes before starting the exercise test, continuously during the exercise test and during 10 minutes immediatly after the end of the exercise test

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jun 2026
  2. Study start19 Oct 2026
  3. Primary completion15 Oct 2031 (estimated)
  4. Study completion31 Mar 2032 (estimated)

Resources

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
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
305 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07671638
Sponsor's protocol ID
ExHyp
Acronym
ExHyp
Status last verified
Oct 2026
First submitted
26 May 2026
Last updated
23 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Mazzeo RS. Physiological responses to exercise at altitude : an update. Sports Med. 2008;38(1):1-8. doi: 10.2165/00007256-200838010-00001.

    PubMed 18081363
  • Hansford HJ, Wewege MA, Cashin AG, Hagstrom AD, Clifford BK, McAuley JH, Jones MD. If exercise is medicine, why don't we know the dose? An overview of systematic reviews assessing reporting quality of exercise interventions in health and disease. Br J Sports Med. 2022 Jun;56(12):692-700. doi: 10.1136/bjsports-2021-104977. Epub 2022 Feb 15.

    PubMed 35168956

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