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Effects of Exercise Timing on Sleep Quality (SLEEPCORE)

C

Centre Hospitalier Universitaire de Saint Etienne

Status

Enrolling

Conditions

Healthy Endurance Athlet
Inactive People

Treatments

Other: Aerobic Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT07322276
25CH122
2025-A00957-42 (Other Identifier)

Details and patient eligibility

About

Modern lifestyles are marked by a prevalence of sedentary behaviors and physical inactivity, which have been linked to numerous adverse health effects. While regular physical exercise is a well-established countermeasure, exercising in the late afternoon may paradoxically disrupt deep sleep due to increased core body temperature. Inactive and sedentary individuals, who often have impaired autonomic function compared to endurance-trained athletes, may be particularly susceptible to these negative effects, potentially resulting in compromised thermoregulation and exacerbated disruptions to deep sleep, a critical stage of sleep essential for overall recovery. Therefore, this study aims to investigate the impact of aerobic exercise performed in the late afternoon versus morning on: 1) deep sleep and sleep onset latency; and 2) core body temperature and its autonomic regulatory mechanisms on endurance-trained and inactive-sedentary people.

Enrollment

42 estimated patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

42 participants in 2 patient groups

"Inactive-sedentary" group
Active Comparator group
Description:
inactive participants that realize 3 experimental conditions: evening exercise, morning exercise and control (no-exercise).
Treatment:
Other: Aerobic Exercise
"Active" group
Experimental group
Description:
endurance athletes that realize 3 experimental conditions: evening exercise, morning exercise and control (no-exercise).
Treatment:
Other: Aerobic Exercise

Trial contacts and locations

1

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Central trial contact

Frédéric ROCHE, PhD

Data sourced from clinicaltrials.gov

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