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Набира участници Не е приложимо NCT07529379

Breathwork and Stress: Investigating the Mechanisms of Action and Effectiveness of Breathing Interventions in Modulating the Psychophysiological Response to Acute Stress Test

Не е приложима фаза (напр. обсервационно)
Заболявания: Healthy Adult Participants Acute Stress Reaction Stress Biomarkers Healthy

Спонсор: Medical University of Bialystok

Налично на: БГ
Обобщение
This study investigates whether the psychophysiological benefits of breathing exercises are driven by a specific physiological rhythm (6 breaths per minute) or by the general psychological experience of performing a structured, mindful activity. Researchers aim to determine if "coherent breathing", which is hypothesized to synchronize heart and respiratory rhythms, offers unique physiological protection against stress compared to breathing at a natural pace or simple resting. The main questions it aims to answer are: * Does slow, steady breathing at 6 breaths per minute lower physical stress markers (like heart rate variability and cortisol) better than faster, but structured breathing or just sitting still? * Is the calming effect caused by the specific breathing rhythm or simply by performing a structured, relaxing activity? Researchers will compare three groups to see if the specific rhythm of "coherent breathing" offers unique benefits: 1. Group (Interventional): Coherent Breathing: Slow breathing at 6 breaths per minute. 2. Group (Sham Breathing): Regular breathing at 15 breaths per minute (matching a natural pace). 3. Spontaneous Breathing (Control Group): Natural, unguided breathing. Participants will: * Complete a one-day preparation phase to become familiar with the breathing technique. * Visit the research center for one experimental session. * Perform their assigned breathing method before and after a stress test. * Take the Maastricht Acute Stress Test (MAST), which involves putting a hand in cold water and doing mental math. * Provide saliva samples and have their heart rate variability, and mood measured multiple times.
Описание
This three-arm randomized controlled trial is designed to investigate whether the therapeutic benefits of slow-paced breathing stem from specific physiological mechanisms (cardiorespiratory resonance) or non-specific psychological factors, such as attention, expectancy, and structured relaxation. The study directly compares resonant-frequency breathing against a structurally identical sham intervention and a passive control group. Experimental Protocol: The study utilizes the Maastricht Acute Stress Test (MAST) as a highly structured and validated laboratory stressor to capture the dynamic psychophysiological response to acute distress. The protocol consists of the following phases: Baseline Phase (BASE): A 5-minute measurement of baseline physiological (HRV - Heart Rate Variability) and psychological (STAI-S - State-Trait Anxiety Inventory-State, VAMS - Visual Analogue Mood Scales) parameters. First Intervention (10 min): Participants perform their assigned breathing technique or sit quietly to assess the preventive "buffering" effect of the intervention. Acute Stress Induction (MAST): A 15-minute structured stressor combining periods of hand immersion in cold water and mental arithmetic under social-evaluative pressure. The water temperature is strictly maintained within the range of 4.5 - 5.5 °C using a TECO chiller to ensure consistent stress induction across all participants. Post-Stress Recovery (POST): Immediate 5-minute measurement following the conclusion of the MAST protocol. Second Intervention (10 min): A repeat of the breathing/control protocol to evaluate its impact on psychophysiological recovery. Final Assessments (END \& FOLLOW): Measurements are taken immediately after the second intervention and following a 15-minute recovery phase to capture the peak glucocorticoid (cortisol) response. Data Collection and Analysis: * Heart Rate Variability: RR interval (time duration between successive heartbeats, specifically the time intervals between each R-wave peak) data is collected using a Polar H10 heart rate monitor. To ensure data integrity and redundancy, the signal is recorded simultaneously through two mobile applications: Elite HRV and Kubios HRV. All subsequent advanced HRV analyses, including time-domain, frequency-domain, and non-linear indices (e.g., PNS/SNS Index \[Parasympathetic Nervous System Index and Sympathetic Nervous System Index\], RMSSD \[Root Mean Square of Successive Differences\]), are performed using Kubios HRV Scientific software. * Biochemical Markers: Salivary cortisol levels are measured to assess the hypothalamic-pituitary-adrenal (HPA) axis response using ELISA kits. * Psychological Scales: Subjective stress and anxiety are tracked using the STAI-VAMS. Adherence Check: Participant adherence to the paced breathing protocols is verified using the Kubios RESP (respiratory rate estimation) algorithm. This software-based solution extracts respiratory frequency from the RR interval data to confirm
Кой може да участва
Inclusion Criteria: * Healthy adults * Aged 18 to 60 years * Willingness to participate in all study phases, including preparation and laboratory session. * Professionally active individuals or university students. Exclusion Criteria: * Severe chronic diseases, including metabolic disorders (e.g., diabetes) and mental disorders. * Cardiac arrhythmia, history of heart attacks, strokes, or heart surgery. * Regular use of medications such as anxiolytics or beta-blockers (excluding hormonal contraception) * Pregnancy. * Current participation in other scientific experiments. * Significant previous experience with breathing techniques or current independent breathwork/meditation practice (defined as regular practice for more than 7 days in total within the last 12 months). * Professional sports practice. * Raynaud's disease * Inability to abstain from alcohol, caffeine, and nicotine for the required periods before the experiment
Интервенции
Coherent Breathing (6 bpm)
BEHAVIORAL
Sham Breathing (15 bpm)
BEHAVIORAL
Места на провеждане 1
Полша (1)
Medical University of Bialystok. Department of Physiology.
Bialystok , Podlaskie Voivodeship
Department of Physiology, Medical University of Bialystok
Технически детайли
Статус
Набира участници
Фаза
Не е приложимо
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Максимална възраст
60 Years
Здрави доброволци
Не
Начална дата
01.04.2026
Крайна дата
01.11.2026
Регистрационен номер
NCT07529379
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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