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

NCT ID: NCT04858815

Last Updated: 2024-10-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

57 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-04-26

Study Completion Date

2022-07-07

Brief Summary

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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.

Detailed Description

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Conditions

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Stress Burnout, Professional

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

single arm longitudinal trial
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Administration of yogic breathing program

This will be a single arm longitudinal trial designed to evaluate the feasibility and estimate the efficacy of implementing a self-administered yogic breathing program for stress reduction among anesthesiology practitioners at one academic medical center.

Group Type EXPERIMENTAL

yogic breathing

Intervention Type BEHAVIORAL

participation in yogic breathing

Interventions

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yogic breathing

participation in yogic breathing

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Medical University of South Carolina

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Grayce Davis, MD

Role: PRINCIPAL_INVESTIGATOR

Medical University of South Carolina

Locations

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Medical University of South Carolina

Charleston, South Carolina, United States

Site Status

Countries

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United States

Other Identifiers

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Pro00105235

Identifier Type: -

Identifier Source: org_study_id

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