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Effects of Moderate Exercise and Cyclic Sighing on Stress, Cognition and Physiological Markers in Young Adults

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07379606
Enrollment
30
Registered
2026-01-30
Start date
2026-07-31
Completion date
2026-10-30
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress

Brief summary

This study investigates the effects of moderate physical exercise and cyclic sighing (breathing training) on stress, cognition, and physiological markers in young adults. It is a randomized cross-over trial with two interventions. Each participant will take part in two intervention sessions: 1. Moderate-intensity physical activity (PA): 15 minutes of stationary cycling at 65-75% of maximum heart rate (HRmax). 2. Breathing training (CS): 15 minutes of cyclic sighing, a technique involving inhaling, pausing briefly, taking a deeper breath, and exhaling slowly. A one-week washout period between sessions is planned to minimise carry-over effects and to ensure participants' physiological state is similar before the next session. During this week, participants will wear Polar Ignite wrist-worn devices to monitor physical activity and sleep. A total of 30 participants (you adults) will be enrolled. Measurements performed before and after each intervention include: * EEG using Emotiv EPOC Flex Gel (32-channel device): 2 minutes with eyes open, 2 minutes with eyes closed, during the interventions, and while performing cognitive test (N-back). * Heart rate variability (HRV) using the Polar H10 sensor. * SUDS - Subjective Units of Disress Scale for perceived stress. * N-back test for cognitive performance using Emotiv App. * Blood pressure (systolic and diastolic) and heart rate. * Pain threshold measured with a dolorimeter. * PANAS-SF - Positive and Negative Affect Schedule. Baseline questionnaires completed by participants the day before the study: * PSS-10 - Perceived Stress Scale (Cohen, Kamarck, Mermelstein). * MAAS - Mindful Attention Awareness Scale * Psychological well-being - short version * Mini-COPE - Coping with Stress Inventory * Sleep quality and average sleep duration * Chronotype questionnaire (morningness-eveningness) * GPAQ - Global Physical Activity Questionnaire * Pittsburgh Sleep Quality Index The study aims to understand how brief interventions like moderate exercise and breathing techniques affect stress, cognitive performance, and physiological responses in young adults.

Interventions

BEHAVIORALModerate-Intensity Physical Activity (PA)

Participants perform 15 minutes of stationary cycling at moderate intensity.

BEHAVIORALBreathing Training - Cyclic Sighing (CS)

Participants perform 15 minutes of cyclic sighing (a breathing technique).

Sponsors

Poznan University of Physical Education
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

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).

Design outcomes

Primary

MeasureTime frameDescription
Mean EEG spectral power in theta, alpha, low beta, high beta, gamma frequency bands during resting-state (eyes-open and eyes-closed)Baseline: immediately before intervention; Post-intervention: immediately after completion of the intervention periodMean spectral power in theta, alpha, low beta, high beta, and gamma frequency bands derived from resting-state EEG recordings collected during eyes-open and eyes-closed conditions. Spectral power will be calculated separately for eyes-open and eyes-closed resting-state conditions.
Heart Rate Variability (HRV)Baseline (average over 5-minute resting-state immediately before intervention); During intervention (average over entire session, periprocedural); Post-intervention (average over 5-minute resting-state immediately after intervention).HRV will be recorded at three time points. Baseline HRV will be calculated as the average over a 5-minute resting-state period immediately before intervention. HRV during the intervention will be calculated as the average over the entire intervention session (periprocedural). Post-intervention HRV will be calculated as the average over a 5-minute resting-state period immediately after intervention.

Secondary

MeasureTime frameDescription
Mean EEG spectral power in theta, alpha, low beta, high beta, and gamma frequency bands during N-back taskBaseline (during N-back task immediately before each intervention session, periprocedural); Post-intervention (during N-back task immediately after each intervention session, periprocedural)Mean spectral power in theta, alpha, low beta, high beta, and gamma frequency bands derived from EEG recordings collected during performance of the N-back cognitive task. Spectral power will be calculated separately for each frequency band and averaged across all EEG channels.
Mean EEG spectral power in theta, alpha, low beta, high beta, and gamma frequency bands during intervention sessionDuring intervention session (periprocedural, averaged over entire session)Mean spectral power in theta, alpha, low beta, high beta, and gamma frequency bands derived from EEG recordings collected during the intervention session. Spectral power will be calculated separately for each frequency band and averaged across all EEG channels.
Perceived Stress measured with the Subjective Units of Distress Scale (SUDS)Baseline: immediately before each intervention session; Post-intervention: immediately after each intervention sessionParticipants rate their perceived stress using the Subjective Units of Distress Scale (SUDS), a self-reported scale ranging from 0 (no stress) to 100 (extreme stress), where higher scores indicate higher perceived stress.
Cognitive Performance (N-back)Baseline: immediately before each intervention session; Post-intervention: immediately after each intervention sessionWorking memory assessed using N-back test with Emotiv app.
Blood PressureBaseline: immediately before each intervention session; Post-intervention: immediately after each intervention sessionSystolic and diastolic blood pressure measured using standard protocols.
Pain ThresholdBaseline: immediately before each intervention session; Post-intervention: immediately after each intervention sessionPain threshold measured using a dolorimeter (algorimeter)
Positive and Negative Affect measured with the Positive and Negative Affect Schedule - Short Form (PANAS-SF)Baseline: immediately before each intervention session; Post-intervention: immediately after each intervention sessionParticipants complete the Positive and Negative Affect Schedule - Short Form (PANAS-SF), a self-reported scale assessing positive and negative affect. Each subscale contains 10 items rated from 1 (very slightly or not at all) to 5 (extremely), giving a possible score range of 10-50 for each subscale. Higher scores indicate higher levels of positive or negative affect, depending on the subscale.
Heart RateBaseline: immediately before each intervention session; Post-intervention: immediately after each intervention sessionHeart rate measured using standard protocols.

Countries

Poland

Contacts

CONTACTBeata Jóźwiak
b.jozwiak@awf.poznan.pl(61) 835 53 49
STUDY_DIRECTORIda Laudańska-Krzemińska

Poznan University of Physical Education

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 4, 2026