Resonance Breathing and Postural Resonance: Acute Modulation of Autonomic and Hemodynamic Responses Via Arterial Baroreflex Mechanisms
Autonomic
2 other identifiers
interventional
30
1 country
1
Brief Summary
This study aimed to compare the acute autonomic and hemodynamic effects of two arterial baroreflex resonance interventions-Resonance Breathing (RB) and Postural Resonance (PR)-in healthy young adults. Methods: A randomized crossover design was conducted in 27 healthy participants (aged 18-25). Each participant completed three experimental sessions (control, RB, and PR) separated by a 5-day washout period. Each session included a 15-minute baseline, a 15-minute intervention, and a 5-min recovery phase. Continuous recordings of skin sympathetic nerve activity (SKNA) and heart rate variability (HRV) were collected throughout each session, while blood pressure (BP) and pulse wave velocity (PWV) were measured before and after the interventions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2024
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 15, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 10, 2026
CompletedFirst Submitted
Initial submission to the registry
April 12, 2026
CompletedFirst Posted
Study publicly available on registry
April 17, 2026
CompletedApril 17, 2026
April 1, 2024
2 months
April 12, 2026
April 12, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Skin sympathetic nerve activity
Skin sympathetic nerve activity (SKNA) was recorded non-invasively at the chest wall using a dedicated SKNA monitoring system. Measurements were obtained at baseline (pre-intervention) and immediately following completion of the resonance breathing and postural resonance intervention, to assess acute changes in sympathetic nervous system activity.
Baseline (pre-intervention) and immediately post-intervention (within 5 minutes of intervention completion)
Secondary Outcomes (2)
Changes in Resting Systolic and Diastolic Blood Pressure
Baseline (pre-intervention) and immediately post-intervention (within 5 minutes of intervention completion)
Changes in Pulse Wave Velocity (PWV)
Baseline (pre-intervention) and immediately post-intervention (within 5 minutes of intervention completion)
Study Arms (1)
Intervention Arm
EXPERIMENTALParticipants receive structured Resonance Breathing and Postural Resonance training aimed at modulating baroreflex function, autonomic balance, and hemodynamic responses. All measurements are conducted at baseline and following intervention.
Interventions
A structured intervention focusing on resonance breathing ( slow, rhythmic breathing at spontaneous resonance frequency ) . The protocol aims to acutely modulate autonomic nervous system activity and hemodynamic responses via stimulation of the arterial baroreflex.
A structured intervention focusing on postural resonance alignment. The protocol aims to acutely modulate autonomic nervous system activity and hemodynamic responses via stimulation of the arterial baroreflex. Sessions include guided breathing practice, postural adjustment, and feedback on breathing mechanics
Eligibility Criteria
You may qualify if:
- years old
You may not qualify if:
- No history of systematic professional sports training; Right-hand dominance (as assessed by the Edinburgh Handedness Inventory). Participants were excluded from the study if they had any of the following: Smoking, chronic alcohol consumption, or the use of psychotropic drugs or other substances affecting the nervous system; Irregular menstrual cycle; History of peripheral neuropathy or other autonomic nervous system disorders; Pre-existing cardiovascular diseases or abnormal electrocardiograms (ECG); Use of hormonal contraceptives; Uncontrolled hypertension or hypotension; Recent major life stressors; Regular practice of meditation or participation in psychotherapy; Presence of any movement disorders or inability to comprehend the experimental instructions.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
No. 11, Gongyi Road, Dongcheng District, Beijing
Beijing, Dongcheng, 100010, China
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 12, 2026
First Posted
April 17, 2026
Study Start
May 1, 2024
Primary Completion
June 15, 2024
Study Completion
April 10, 2026
Last Updated
April 17, 2026
Record last verified: 2024-04