Breathing Practice to Improve Resilience and Mental Well-Being in Healthcare Professionals Experiencing Burnout
Led by Mayo Clinic · Updated on 2026-11-02
40
Participants Needed
4
Research Sites
N/A
Total Duration
AI-Summary
What This Trial Is About
This study evaluates the immediate and long-term effects of structured breathing exercises on mental health symptoms such as anxiety, depression, perceived stress, and sleep quality in healthcare professionals. The research aims to understand how breathing practices might support mental well-being and resilience in this population.
Participants will engage in self-guided structured breathing sessions lasting 15, 30, or 36 minutes, tailored to their personal skill level. These sessions are designed to improve brain circulation and mental well-being. The study uses a single group design without a comparison group, focusing on this breathing intervention over a four-month period.
Throughout the study, participants will use a mobile app to track adherence, engagement, and satisfaction with the breathing exercises. Researchers will assess feasibility through recruitment ease, retention rates, and intervention acceptability. Mental health outcomes and participant feedback will be collected at regular intervals during the four months of study participation.
CONDITIONS
Brief Title
A Study Of Resilience And Mental Well-Being Through Breathing Practice For Clinical Care Professionals
Research Team
D
Danielle Boos
P
Paul Min, PhD
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This table compares participation in this trial with other options available for this condition. The information is drawn from published research and the trial’s study details and is provided for educational purposes only.
Factors
Structured Breathing Intervention
Mobile or Online Mindfulness-Based Programs
What the intervention is
A structured breathing-based behavioral program delivered mainly online via a mobile application with sessions of 15, 30, or 36 minutes chosen by participants.
Mobile or online mindfulness-based programs that use guided exercises to reduce stress and burnout among healthcare professionals.
Role in the study
The single investigational intervention tested in a feasibility study design.
Serves as a non-randomized external comparator based on existing digital mindfulness tools used in clinical contexts.
Primary purpose
Feasibility and acceptability of a breathing-based intervention to support resilience and well‑being among clinicians.
Widely used to reduce burnout, build resilience, and improve psychological well‑being among healthcare staff.
How it is delivered
Self‑guided structured breathing sessions via a mobile app, lasting 15 to 36 minutes, over a 4‑month period.
Delivered online or via mobile platforms through guided audio or video mindfulness sessions, often over several weeks.
Evidence for efficacy or feasibility
Feasibility and acceptability are being evaluated; effectiveness outcomes not yet reported.
Evidence from randomized trials shows significant reductions in burnout and related psychological stress among nurses and healthcare professionals.
Important risks
General behavioral intervention risks only; no specific safety concerns identified at this stage.
Generally considered low‑risk as non‑invasive wellness tools with minimal safety issues.
Limitations
Single‑group design without comparator limits conclusions about effectiveness beyond feasibility.
Findings derive from varied programs and are not tied to a standardized structured breathing protocol.
Disclaimer: This comparison is created with the help of artificial intelligence(AI) and may contain errors or missing information. It is not medical advice and does not mean one option is better or safer than another. Clinical trials are still being studied, and joining a trial is your choice. Please consult your healthcare professional before making any decisions.
Who Can Participate
Age: 18Years - 85Years
All Genders
Healthy Volunteers
Eligibility Criteria
You may qualify if you...
Participants must be healthcare professionals at the specified four Mayo Clinic Health System sites.
Must have a Copenhagen Burnout Inventory score of 40 or higher.
Must be physically fit enough to perform light exercise.
Must read and understand English to consent, complete measures, and follow instructions.
Must have access to a smartphone or tablet.
You will not qualify if you...
Active primary psychotic disorder or substance use disorder (except nicotine dependence) within the past year.
Severe or unstable medical condition interfering with participation or data collection.
Active neurological condition such as seizure disorder, traumatic brain injury, or stroke affecting cognition or brain imaging.
Chronic lung disease like COPD or cystic fibrosis, or aneurysm.
Current pregnancy or planning to become pregnant during the study period.
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or virtual)
Breathing Intervention
Duration - 4 months
Participants engage in self-guided structured breathing sessions designed to improve mental well-being and brain circulation.
Regular mobile app engagement and periodic assessments
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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Published Research Related To This Trial
Evaluation of a structured breathing-based intervention to reduce burnout and enhance mental well-being among healthcare professionals in community-based practice settings: study protocol for a single-arm pilot feasibility trial.