NCT07218458 A Study Of Resilience And Mental Well-Being Through Breathing Practice For Clinical Care Professionals
| NCT ID | NCT07218458 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Mayo Clinic |
| Condition | Burnout, Healthcare Workers |
| Study Type | INTERVENTIONAL |
| Enrollment | 40 participants |
| Start Date | 2025-10-27 |
| Primary Completion | 2026-09-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 40 participants in total. It began in 2025-10-27 with a primary completion date of 2026-09-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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.
Eligibility Criteria
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
Contact & Investigator
Pravesh Sharma, MD
PRINCIPAL INVESTIGATOR
Mayo Clinic
Frequently Asked Questions
Who can join the NCT07218458 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 85 Years, studying Burnout, Healthcare Workers. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07218458 currently recruiting?
Yes, NCT07218458 is actively recruiting participants. Contact the research team at boos.danielle@mayo.edu for enrollment information.
Where is the NCT07218458 trial being conducted?
This trial is being conducted at Albert Lea, United States, Mankato, United States, Eau Claire, United States, La Crosse, United States.
Who is sponsoring the NCT07218458 clinical trial?
NCT07218458 is sponsored by Mayo Clinic. The principal investigator is Pravesh Sharma, MD at Mayo Clinic. The trial plans to enroll 40 participants.