Influence of Training Session Duration on Improvements in Physiological Resilience to Exercise

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-45
SponsorCentre Hospitalier Universitaire de Saint Etienne

About this trial

During prolonged endurance exercise, certain physiological variables deteriorate depending on the duration of the exercise. Physiological resilience has therefore been defined as the ability to resist these changes and appears to be an important performance factor in endurance sports. For example, most studies in this field have investigated changes in cycling power output associated with the first ventilatory threshold (VT1), a marker of an individual's endurance capacity, after prolonged endurance exercise. To date, only two studies have examined the effects of training on resilience. The first compared the effectiveness of two training programs, one with low-intensity sessions and the other with high-intensity sessions, with no difference between the conditions. The second study showed that incorporating strength training into a running training program was more effective at improving resilience than running alone. However, the influence of training session duration on resilience remains unknown. Only one observational study has shown that in a group of runners of similar ability, those who were used to doing long sessions had better resilience than those who only did short sessions.

Eligibility criteria

Qualifiers

Subjects who engage in rigorous cardiovascular activity (e.g., endurance sports, team sports, combat sports, etc.) for a maximum of two hours per week

Ability to understand, speak, read, and write French

Affiliated with or beneficiaries of a social security system

Having freely given their written consent after being informed of the purpose, procedure, and potential risks involved

Disqualifiers

Subjects with chronic joint conditions (e.g., recurrent sprains, patellar or ligament problems).

Subjects with one or more heart conditions, including ischemic, valvular, arrhythmic, hypertensive, congenital, or hypertrophic heart disease.

Participants under guardianship or conservatorship.

Subjects with chronic or central neurological conditions.

Trial design

Treatments tested in this trial

  • Long sessions
  • Short sessions

Treatment groups

40 Participants
are divided into 2 treatment groups