Skip to content

FACEFI : Cardiac Fatigue During Intense Exercises - Pilot Study

FACEFI : Cardiac Fatigue During Intense Exercises - Pilot Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02126891
Acronym
FACEFI
Enrollment
23
Registered
2014-04-30
Start date
2014-01-31
Completion date
Unknown
Last updated
2015-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle; Fatigue, Heart

Keywords

Cardiac functions, Endurance training, Senior athletes

Brief summary

To attest if a cardiac fatigue appears (and to measure it if it does) during intense physical exercises in two groups of subjects: * Canoeists from a training center of the French canoeing team during an intensive session of three weeks of endurance training; * Young recruits in military school of officers in ground forces of the French army during an intensive.

Interventions

PROCEDURETests

Individual parameters of echocardiography and heart rate variability

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy men between 18 and 35 years old; * Giving their writing informed consent; * And affiliated to the French social security.

Exclusion criteria

* To be a smoker. * To present any known pathology that forbids the realisation of any test, or that can alter the measurements: cardiovascular risk factors treated or not (diabetes, dyslipidaemia, arterial hypertension, obesity), cardiac arrhythmia, coronary disease, heart failure, cardiac pacemaker or defibrillator, valvular disease after surgery or not, kidneys failure with dialyse or not, kidney pulmonary cardiac or liver transplantation, chronic bronchopneumopathy, asthma, etc. * To take any medication that could alter autonomic nervous system or cardiovascular adaptation to maximal exercise (anti-arrhythmia, anti-hypertensive, anti-inflammatory,…). * Drinking exciting drinks (coffee or tee for example) in the 12h before the tests. * To be under legal protection (trusteeship, guardianship) or to be deprived of liberty.

Design outcomes

Primary

MeasureTime frameDescription
Measure of classical echocardiographic parameters to attest systolic and diastolic functionsday 8 (canoeists) / day 5 (military)Speckle tracking will also be used to get strain parameters of the left ventricle. Measure will by recording daily before, during, and after a period of intensive training, in order to attest possible cardiovascular effects of such periods. Echocardiographic data will be recorded at rest and during a submaximal exercise.

Secondary

MeasureTime frameDescription
Measure of classical heart rate variability parametersday 8 (canoeists) / day 5 (military)Measure will by recording daily before, during, and after a period of intensive training, in order to attest possible cardiovascular effects of such periods. Measure will be recorded during 5 min resting and 5 min standing.

Countries

France

Contacts

Primary ContactFrançois FC Carré
francois.carre@chu-rennes.fr33-2-9928-3750

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026