NCT07536997

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2024

Completed
1.8 years until next milestone

Study Completion

Last participant's last visit for all outcomes

April 10, 2026

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

April 12, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

April 17, 2026

Completed
Last Updated

April 17, 2026

Status Verified

April 1, 2024

Enrollment Period

2 months

First QC Date

April 12, 2026

Last Update Submit

April 12, 2026

Conditions

Keywords

Arterial baroreflexAutonomic nervous systemSkin sympathetic nerve activityBlood pressureResonance intervention

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

EXPERIMENTAL

Participants 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.

Behavioral: Resonance BreathingBehavioral: Postural Resonance

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.

Intervention Arm

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

Intervention Arm

Eligibility Criteria

Age18 Years - 30 Years
Sexall(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Location

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

Locations