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NCT Number: NCT07650279

Coherence Breathing Before Cardiopulmonary Exercise Testing

This randomized crossover trial will examine the acute effects of pre-exercise coherence breathing on cardiopulmonary exercise responses in recreationally active adults. Participants will complete two experimental conditions in randomized order: 5 minutes of guided coherence breathing and 5 minutes of quiet seated spontaneous breathing. Following each condition, participants will perform a standardized treadmill warm-up and a maximal cardiopulmonary exercise test. Outcomes will include oxygen consumption, heart rate, heart rate recovery, perceived exertion, time to completion, and heart rate variability. The findings may help determine whether coherence breathing can serve as an effective autonomic priming strategy before a bout of maximal exercise

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Key information

Age range

19 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Slow-paced breathing performed at approximately six breaths per minute has been shown to influence autonomic nervous system activity and heart rate variability. Coherence breathing may improve physiological regulation by enhancing cardiorespiratory synchronization and vagal modulation. However, little is known about whether a brief bout of coherence breathing performed immediately before exercise can influence cardiopulmonary exercise performance. The purpose of this study is to investigate the acute effects of pre-exercise coherence breathing on cardiopulmonary exercise performance and autonomic responses in recreationally active adults. This study will utilize a randomized, counterbalanced crossover design. Recreationally active adults aged 19 to 45 years will complete two experimental conditions in random order separated by a minimum of 48 hours (maximum of 7 days). In one condition, participants will perform 5 minutes of guided coherence breathing using a visual breathing pacer at approximately 6 breaths per minute while seated. In the comparison condition, participants will sit quietly for 5 minutes with spontaneous breathing. Following each condition, participants will complete a standardized treadmill warm-up and a maximal cardiopulmonary exercise test (CPET). Heart rate variability will be assessed during baseline seated rest and during the breathing intervention. Cardiopulmonary variables collected during CPET will include oxygen consumption, heart rate, respiratory responses, and ratings of perceived exertion. Recovery responses over 5 minutes seated include heart rate and blood pressure will also be assessed following exercise.

Findings from this study may improve our understanding of breathing strategies for athletic performance. Specifically, whether slow paced breathing through coherence breathing can serve as a practical autonomic priming strategy before maximal exercise. Moreover, insights from this study may provide insight into the acute interaction between breathing regulation, autonomic function, and exercise responses.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 19 to 45 years.
  • Any biological sex.
  • Recreationally active, defined as accumulating at least 3 hours per week of moderate-to-vigorous physical activity.
  • Able to perform maximal cardiopulmonary exercise testing on a treadmill.
  • Able to provide informed consent.
  • Cleared for moderate-to-vigorous physical activity based on the PAR-Q+ (or PAR-Q 2023).

Exclusion criteria

  • Accumulate less than 3 hours per week of moderate-to-vigorous physical activity.
  • Presence of a health condition that contraindicates maximal exercise testing, including:

Cardiovascular disease. Pulmonary disease. Metabolic disorders. Neuromuscular disorders. Orthopedic limitations that impair exercise performance.

  • Acute illness that would interfere with participation or exercise testing.
  • Inability or unwillingness to complete study procedures.
  • Inability or unwillingness to provide informed consent.
  • Not cleared for moderate-to-vigorous physical activity based on the PAR-Q+ (or PAR-Q+ 2023).

Treatment and study plan

Coherence Breathing

Behavioral

Participants complete 5 minutes of guided coherence breathing which consists or around 6 breathing cycles (5 seconds inhale and 5 seconds exhale)

Other names: slow-paced breathing, resonance breathing

Spontaneous Breathing

Behavioral

Participants sit quietly for 5 minutes with their regular spontaneous breathing

Primary outcomes

  1. Peak Oxygen consumption

    Time frame: during each maximal exercise test immediately after the breathing condition

    Peak oxygen consumption measured during the maximal cardiopulmonary exercise test (CPET) using a portable metabolic analyzer (Vo2 Master)

Secondary outcomes

  1. rating of perceived exertion (RPE)

    Time frame: measured at baseline, during the exercise test and after recovery

    using the RPE borg scale (from 1-10)

  2. Heart Rate Recovery

    Time frame: difference between peak HR during CPET and HR at minute 1, minute 2 and minute 5 of recovery.

    Heart Rate (bpm) immediately after completing the CPET over a period of 5 minutes

  3. Time to completion of maximal exercise test

    Time frame: during the exercise test

    total duration of the exercise test since test starts to voluntary termination

  4. Peak Heart Rate

    Time frame: measured during the maximal exercise test

    maximal heart rate achieved during the maximal exercise test

Study contacts

Contact information is provided by the study sponsor or research team.

Jaime Pigman, PhD

CONTACT

[email protected]

732-749-0160

Tamara Rial-Faigenbaum, PhD

CONTACT

[email protected]

2159878984

Sponsors and collaborators

Lead sponsor

Human Performance Lab of Monmouth University

Other

Registry information

Official study title

Acute Effects of Coherence Breathing on Cardiopulmonary Exercise Responses in Recreationally Active Adults: A Randomized Crossover Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 16, 2026
Registry last updated
Jun 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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