Clinical trial Recruiting at 1 site Interventional Ages 18 to 30

Morning versus late-afternoon aerobic exercise: effects on sleep in endurance athletes and inactive people

Official title: Effects of Exercise Timing and Physical Activity Level on Sleep Quality and Body Temperature

Run by Centre Hospitalier Universitaire de Saint Etienne · NCT07322276 · Data updated 2026-11-12

This trial will test if doing aerobic exercise in the morning versus the late afternoon changes deep sleep, how quickly you fall asleep, and core body temperature in endurance athletes and inactive adults.

Quick facts

Study typeInterventional
Ages18 Years to 30 Years
SexAll
Enrollment42 (estimated)
SponsorCentre Hospitalier Universitaire de Saint Etienne
Academic / other
Locations1 site (Saint-Etienne)
StatusRecruiting
StartedJanuary 23, 2026
Main results expectedJanuary 31, 2029
Study endsMay 31, 2029
Registry record updatedJune 3, 2026
Trial IDNCT07322276 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Healthy adults who are either endurance-trained athletes (specializing in aerobic exercise with >300 minutes/week for at least 6 months and regional-level participation) or inactive/sedentary adults who do not meet WHO exercise recommendations, and who do not have excluded medical or sleep conditions.

Probably not a fit

People with diagnosed sleep disorders, significant medical conditions (renal, respiratory, cardiovascular, neuromuscular), current mental health conditions requiring treatment, or who are pregnant or breastfeeding are excluded and unlikely to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Participants who are either endurance-trained athletes or inactive, sedentary adults will be assigned to perform standardized aerobic exercise sessions in the morning or late afternoon. The study will record sleep architecture with emphasis on deep sleep and sleep onset latency, and will continuously monitor core body temperature and autonomic markers such as heart rate variability. Investigators will compare effects of exercise timing within and between the two participant groups to determine whether training status modifies these responses. The protocol involves supervised in-person exercise sessions and physiological monitoring at a single center.

Why it matters

Potential benefit: If positive, the findings could guide when people should schedule aerobic workouts to improve deep sleep and recovery.

How similar studies have gone: Previous research shows regular exercise can improve sleep overall, but evidence about the specific effects of exercise timing on deep sleep and core temperature is mixed and relatively limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Group "Inactive" :No regular exercise practice (inactive people that don't follow the WHO recommendations) and have sedentary behaviors
* Group "Active": Regular exercise (athletes that are specialized in aerobic exercise, with more than 300 minutes per-week over 6 months and practice at regional level).

Exclusion Criteria:

* Have sleep disorders medically diagnosed or detected by sleep forms cutoffs (clinical insomnia by ISI, severe risk of obstructive sleep apnea by Stop-Bang, bad sleep quality by PSQI.
* Have a diagnosed mental health condition requiring treatment
* Have renal, respiratory, cardiovascular or neuromuscular disease medically diagnosed.
* Be pregnant or breastfeeding

Where it's running

  • Chu Saint-Etienne
    Saint-Etienne, France
    Recruiting

Study contacts

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.