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A Study Of Resilience And Mental Well-Being Through Breathing Practice For Clinical Care Professionals

Enhancing Resilience And Mental Well-Being Through Breathing Practice For Clinical Care Professionals (Breathing Study-Burnout)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07218458
Enrollment
40
Registered
2025-10-20
Start date
2025-10-27
Completion date
2026-11-30
Last updated
2026-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breathing Exercises, Burnout, Healthcare Workers

Keywords

burnout, breathing

Brief summary

The purpose of this study is to assess the immediate and long-term effects of structured breathing on clinical symptoms related to mental health including anxiety, depression, perceived stress, and sleep quality.

Interventions

BEHAVIORALStructured Breathing

15, 30, or 36 minute structured breathing sessions based on personal skill level.

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants must be healthcare professionals at the above-mentioned 4 MCHS sites (Eau Claire, La Crosse, Mankato, Albert Lea). * Must score ≥40 on Copenhagen Burnout Inventory Q1-6. * Participants must be physically fit enough to perform light exercise. * Participants should read and understand English well enough to consent, complete measures, and follow instructions. * Participants must have access to a smartphone or tablet.

Exclusion criteria

* Active primary psychotic disorder or substance use disorder (except nicotine dependence) within the past year. * Severe or unstable medical condition that could interfere with participation or data collection. * Active neurological condition (including seizure disorder, traumatic brain injury, or stroke) that could affect cognitive functioning or brain imaging results. * Chronic lung disease (e.g., COPD, cystic fibrosis) or aneurysm. * Current pregnancy or planning to become pregnant during the study period

Design outcomes

Primary

MeasureTime frameDescription
Assess feasibility of the structured breathing-based intervention among healthcare professionals via ease of recruitmentEnrollment to end of study participation at 4 months.This outcome measure will assess whether the structured breathing-based intervention is feasible among healthcare professionals via ease of recruitment reported by study staff.
Assess feasibility of the structured breathing-based intervention among healthcare professionals via retention statisticsEnrollment to end of study participation at 4 monthsThis outcome measure will assess the feasibility of the structured breathing-based intervention among healthcare professionals by examining retention rates throughout study duration.
Assess feasibility of the structured breathing-based intervention among healthcare professionals via mobile app engagement metricsEnrollment to end of study participation at 4 monthsThis outcome measure will assess whether the structured breathing-based intervention is feasible among healthcare professionals by analyzing app usage metrics from participants.
Assess feasibility of structured breathing-based intervention among healthcare professionals via Feasibility of Intervention MeasureEnrollment to end of study participation at 4 monthsTo assess the feasibility of a structured breathing intervention among healthcare professionals using Feasibility of Intervention Measure (FIM). Feasibility of Intervention Measure is a four-item measure of implementation feasibility with scores ranging from 1-5, with higher scores indicating greater feasibility.
Assess appropriateness of structured breathing-based intervention among healthcare professionalsEnrollment to end of study participation at 4 monthsTo assess the appropriateness of a structured breathing intervention among healthcare professionals using Intervention Appropriateness Measure (IAM). Intervention Appropriateness Measure is a four-item measure with a scale of responses from 1-5, with higher scores indicating greater appropriateness.
Assess acceptability of structured breathing-based intervention among healthcare professionalsFrom enrollment to the end of study participation at 4 monthsTo assess the acceptability of a structured breathing intervention among healthcare professionals utilizing the Acceptability of Intervention Measure (AIM). Acceptability of Intervention Measure is a four-item measure with responses from 1-5, with higher scores equating to greater acceptability.
Assess participant satisfaction related to breathing-based interventionEnrollment to end of study participation at 4 months.Participant satisfaction will be assessed through a mixed-methods approach combining quantitative surveys (exit survey) and qualitative participant interviews (4 month in-person visit/interview).

Secondary

MeasureTime frameDescription
Evaluate intervention adherence, usability, and engagement metrics via mobile applicationEnrollment to end of treatment at 4 months.To evaluate the breathing intervention adherence, usability, and engagement metrics collected through the mobile application platform. These data will be used to identify barriers and facilitators to digital engagement, assess usability, and inform refinements to the intervention's delivery and technological infrastructure for future large-scale trials.

Countries

United States

Contacts

CONTACTDanielle Boos
boos.danielle@mayo.edu715-464-8173
CONTACTPaul Min, PhD
min.paul@mayo.edu507-255-2814
PRINCIPAL_INVESTIGATORPravesh Sharma, MD

Mayo Clinic

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 6, 2026