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OpenTrials
Completed

NCT Number: NCT04858815

Using Yogic Breathing to Reduce Stress in Anesthesia Personnel As Measured by Hair Cortisol

Mind body exercises have long been used as a way for individuals to reduce stress and improve well-being. Recent studies indicate that yogic breathing (YB, also known as pranayama) could potentially impact both the mind and body by engaging both the physiological and neural elements and can thus be a specific tool that can be utilized by healthcare workers to combat burnout and decrease perceived levels of stress. Our aim is to understand and measure both subjectively and objectively the effects of long-term yogic breathing on stress levels in anesthesia personnel. This will be a single arm longitudinal trial designed to evaluate the feasibility and estimate the efficacy of implementing a yogic breathing program for stress reduction among anesthesiology practitioners at one academic medical center. The primary aim of the trial is to estimate the correlation between participant stress with average duration of yogic breathing over time. Secondarily the feasibility of implementing yogic breathing practices among anesthesiology practitioners will be evaluated. Feasibility measures will include recruitment rates, retention at 1year follow-up, and adherence to the yogic breathing program at 12 months.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Medical University of South Carolina

Charleston, South Carolina, 29425, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • All clinical members of the MUSC anesthesia department (Attending physicians, resident physicians, and CRNAs)

Exclusion criteria

  • Pregnancy (or anticipated pregnancy)
  • chronic steroid use
  • inadequate hair length for testing (less than 3cm at the back of the head)
  • residents with anticipated graduation within the next one year.

Treatment and study plan

yogic breathing

Behavioral

participation in yogic breathing

Primary outcomes

  1. Correlation of participant stress with average duration of yogic breathing over time

    Time frame: baseline & 12 month visit

    The study will estimate the efficacy of self-administered yogic breathing on participant stress over time using (a) cortisol levels measured in hair and (b) using validated survey instruments estimated as the change in stress from baseline to 12 months. The primary measure of efficacy is correlation between cortisol/stress levels with average weekly duration of yogic breathing in minutes.

Sponsors and collaborators

Lead sponsor

Medical University of South Carolina

Other

Registry information

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Apr 26, 2021
Registry last updated
Oct 24, 2024

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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