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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03946215
Other study ID # 7038
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2018
Est. completion date December 17, 2018

Study information

Verified date May 2019
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is: i) to determine if maximal oxygen uptake in downhill running is significantly different versus flat or uphill running, and ii) to compare cardiorespiratory and muscle fatigue responses to uphill vs flat and downhill running at similar running velocity and similar metabolic power. The investigators hypothesized that maximal oxygen uptake will be lower in downhill running. The investigators also anticipate attenuated cardiorespiratory and muscle fatigue responses to downhill running when compared to flat or uphill running performed at similar velocity but not when the comparison is done at similar metabolic power.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date December 17, 2018
Est. primary completion date December 17, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- to be a well-trained runner with a VO2max > à 55 ml/kg/min

- nonsmoker or stopped smoking for 5 years

- BMI < 25

- affiliation to the social health insurance scheme

- signing an informed consent form.

Exclusion criteria:

- impossibility to give the subject enlightened information (subject in emergency situation, difficulties in understanding the study, ...);

- subject under the protection of justice

- subject under guardianship or curatorship

- contraindication to the practice of physical and sport activities

- lower limbs musculotendinous or articular problems

- respiratory, cardiovascular or metabolic pathology

- drug treatment in progress and impossibility to stop it within 7 days before the beginning of the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Each participant will perform:
Part 1: Maximal incremental tests will require running at fixed slopes (+15%, 0% -15%) for stages (2min duration) of increasing velocities (0.5, 1 and 1.5 km/h) Part two: submaximal running tests will require running at constant velocity (80% VO2max uphill; 80%VO2max downhill and downhill at similar velocity as uphill)

Locations

Country Name City State
France Les Hôpitaux Universitaires de Strasbourg Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Peak oxygen The peak oxygen uptake will be collected during downhill, flat and uphill running 15 minutes
See also
  Status Clinical Trial Phase
Completed NCT04075929 - Short or Long High Intensity Training N/A