Clinical trial Recruiting at 1 site Interventional Ages 18 to 50

Sleep extension to reduce performance loss from sleep deprivation

Official title: Effect of Sleep Extension in Prevention to Sleep Deprivation on Running Endurance Performance

Run by Centre Hospitalier Universitaire de Saint Etienne · NCT06928168 · Data updated 2026-11-12

This trial tests whether adding extra sleep in the days before long runs helps healthy adult runners resist the fatigue and performance decline caused by partial or total sleep deprivation.

Quick facts

Study typeInterventional
Ages18 Years to 50 Years
SexAll
Enrollment69 (estimated)
SponsorCentre Hospitalier Universitaire de Saint Etienne
Academic / other
Locations1 site (Saint-Etienne)
StatusRecruiting
StartedJune 12, 2025
Main results expectedJanuary 1, 2028
Study endsMarch 1, 2028
Registry record updatedOctober 9, 2026
Trial IDNCT06928168 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Healthy men and women aged 18–50 who run at least one session longer than one hour per week, normally sleep 6–8 hours per night, have no chronic medical conditions, and are not shift workers or currently in competition.

Probably not a fit

People with chronic illnesses, night-shift workers, those with sleep disorders or excessive daytime sleepiness, or those whose usual sleep falls outside 6–8 hours may not be represented and therefore may not benefit from the results.

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

What this trial studies

Healthy adults who run regularly will follow a period of either their usual sleep or prescribed sleep extension in the days before a prolonged running exercise. Participants will then be exposed to partial or total sleep deprivation and complete endurance running tests while researchers record performance, rate of perceived exertion (RPE), and fatigue measures. The protocol explicitly examines reproducibility of effects and individual differences in resistance to sleep loss. Outcomes will compare whether prior sleep extension lessens the negative impact of sleep deprivation on sustained running performance.

Why it matters

Potential benefit: If successful, this could provide a simple, low-risk strategy—getting extra sleep before events—to reduce fatigue and help preserve endurance performance during sleep-deprived competitions.

How similar studies have gone: Small prior studies suggest sleep extension before endurance events can reduce perceived exertion and partly protect performance under sleep loss, but published evidence is limited and reproducibility remains uncertain.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Volunteer who signed the written consent form.
* Man or woman.
* Aged 18-50.
* Physically active and running at least one session of more than one hour per week.
* Haven't participated in any competition in the month before the first visit.
* Not participating in any competition during the study.
* Usual sleep time between 6h-8h per night.

Exclusion Criteria:

* \- Any chronic pathology.
* Working night shift.
* Having sleep disorders: score \> 5 at Pittsburg Sleep Quality Index.
* Excessive sleepiness: score \>10 at Epworth Sleepiness scale.

Where it's running

  • FEASSON Léonard
    Saint-Etienne, France
    Recruiting

Study contacts

  • Principal investigator: Frédéric ROCHE, PhD — Centre Hospitalier Universitaire de Saint Etienne
  • Study coordinator: Diana RIMAUD, science Doctor
  • Email: Diana.Rimaud@chu-st-etienne.fr
  • Phone: 0477120467

Similar studies

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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.