Clinical trial Recruiting at 1 site Interventional Ages 18 to 35

Effects of Moderate Exercise and Cyclic Breathing on Stress and Cognition in Young Adults

Official title: A Comparison of Psychophysiological Effects Between Relaxation Techniques and Physical Exercise in Young Adults

Run by Poznan University of Physical Education · NCT07379606 · Data updated 2026-11-12

This study tests whether 15 minutes of moderate exercise or 15 minutes of cyclic sighing can affect stress, thinking skills, and body signals in healthy young adults.

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Quick facts

Study typeInterventional
Ages18 Years to 35 Years
SexAll
Enrollment30 (estimated)
SponsorPoznan University of Physical Education
Academic / other
Locations1 site (Poznan, Wielkopolska)
StatusRecruiting
StartedJuly 31, 2026
Main results expectedApril 30, 2027
Study endsApril 30, 2027
Registry record updatedNovember 2, 2026
Trial IDNCT07379606 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are healthy adults aged 18–35 without chronic diseases, psychiatric disorders, or regular use of psychotropic medications, and with stable sleep in the week before participation.

Probably not a fit

Individuals with contraindications to moderate physical activity, EEG incompatibilities, active psychiatric conditions, or recent substance use or caffeine intake near the study sessions may not benefit.

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

What this trial studies

This randomized cross-over trial compares two 15-minute interventions in 30 healthy adults aged 18–35: moderate-intensity stationary cycling and a breathing training called cyclic sighing. Each participant experiences both interventions with a one-week washout period between sessions. Physiological data will be collected via wearable activity trackers and EEG measurements before and after each intervention to explore short-term effects on stress markers and cognitive function. The study is conducted at the Poznan University of Physical Education with each participant serving as their own control to reduce variability.

Why it matters

Potential benefit: If successful, the study could identify simple, nonpharmacological strategies to help manage stress and support cognitive function.

How similar studies have gone: Previous research has shown short-term stress and cognitive responses to exercise and breathing techniques, but this exact cross-over design with EEG and wearables is relatively novel in this population.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* male or female participants,
* age 18-35,
* without chronic somatic diseases,
* no current episode of psychiatric disorder (no active depression, mania, or psychosis),
* regular sleep schedule in the week prior to the study,
* not taking psychotropic drugs or medications,
* non-smoker,
* not working nightshifts.

Exclusion Criteria:

* consumption of alcohol or psychoactive substances the day before or on the day of the study,
* intense physical activity less than 2 hours before the study,
* consuming coffee, black tee, energy drinks less than 2 hours before the study,
* contraindications to moderate-intensity physical activity on cycle ergometer (e.g., recent injuries),
* contraindications to EEG (e.g., scalp skin conditions preventing proper electrode placement, hypersensitivity to conductive gels or pastes).

Where it's running

  • Poznan University of Physical Education
    Poznan, Wielkopolska, Poland
    Recruiting

Study contacts

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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.