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Burn OutNCT07018609

Mitigating Burnout in Nursing and Associated Healthcare Staff

A study testing Zen Den Experience and Music Therapy Experience in people with Burn Out and Nurses, run by Milton S. Hershey Medical Center.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Workplace stress for healthcare workers is at an all-time high and the COVID-19 Pandemic magnified and amplified the impact of stress and burnout on health care workers, especially for frontline staff such as nurses. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Burn Out, Nurses
What is being tested?
Zen Den Experience and Music Therapy Experience
Could I receive a placebo?
No, everyone receives an active treatment
How many people
300 participants
Where
No sites listed yet
Study dates
1 Sep 2027to 30 Apr 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • English-speaking employees or students at Penn State Health and College of Medicine.

Who cannot join

  • Non-English speaking individuals

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

About this study

Official title: The Zen Den - Mitigating Burnout in Nursing and Associated Healthcare Staff

Workplace stress for healthcare workers is at an all-time high and the COVID-19 Pandemic magnified and amplified the impact of stress and burnout on health care workers, especially for frontline staff such as nurses. There are multiple external and individual factors that affect clinician well-being, and organizational factors are an important aspect to address when attempting to mitigate nurse burnout and improve well-being. This project seeks to expand two interventions that were piloted in the last few years since the Covid-19 Pandemic, validated to show improvement in staff well-being and decreased feelings of burnout following the interventions, and are easily implemented to benefit nurses and other multidisciplinary health care workers and students in both the inpatient and outpatient settings.

Conditions
Burn Out, Nurses
Being tested
Zen Den Experience, Music Therapy Experience
Keywords
Burnout, Nurses, Music Therapy
Medical subject headings
Burnout, Psychological

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Zen Den ExperienceBehavioural

    The Zen Den is a dedicated safe space for healthcare staff to decompress and recharge during shifts, addressing the growing issue of workplace stress. It has soft warm lighting, sound machines and aroma therapy, relaxing furnishings centered around a faux fireplace to create a stress-free environment.

  • Music Therapy ExperienceBehavioural

    The music therapy experience will consist of either Music Minutes which have music therapists available on specific units and circulating amongst staff across flexible shift times. Intervention choices will include relaxation songs, motivation songs, music, mindfulness, breathing to music, dance-a-minute, and brief song rewrites. Notes for Resilience will be scheduled group sessions that follow a more structured format and are 30 to 60 minutes in length. Involvement and coping will be emphasized through active forms of music participation, including drum circles, unit playlist creation, song writing, jam sessions, and song discussion.

Study groups in NCT07018609
Study groupRoleWhat they receive
Zen DenActive comparatorZen Den
Receives: Behavioral: Zen Den Experience
Music TherapyActive comparatorNot described
Receives: Behavioral: Music Therapy Experience

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The number of subjects who state preference for having long-term access to the intervention.

    This will be measured on a Likert scale where 0 is strongly disagree and 5 is strongly agree

    Measured: Survey data will be collected at the end of the intervention up to 30 minutes post intervention.

  2. The number of subjects who report improvement of subject's energy level needed to complete immediate job responsibilities.

    This will be measured on a Likert scale where 0 is strongly disagree and 5 is strongly agree

    Measured: Survey data will be collected at the end of the intervention up to 30 minutes post intervention.

  3. The number of subjects who report improvement of subject's understanding of what is needed in the moment to overcome challenges.

    This will be measured on a Likert scale where 0 is strongly disagree and 5 is strongly agree

    Measured: Survey data will be collected at the end of the intervention up to 30 minutes post intervention.

  4. The number of subjects who report improvement navigating challenging or difficult situations in the workplace

    This will be measured on a Likert scale where 0 is strongly disagree and 5 is strongly agree

    Measured: Survey data will be collected at the end of the intervention up to 30 minutes post intervention.

  5. The number of subjects who report improvement in expressing thoughts, questions and feelings with colleagues situations in the workplace.

    This will be measured on a Likert scale where 0 is strongly disagree and 5 is strongly agree

    Measured: Survey data will be collected at the end of the intervention up to 30 minutes post intervention.

  6. The number of subjects who report improvement in feeling less isolated at work.

    This will be measured on a Likert scale where 0 is strongly disagree and 5 is strongly agree

    Measured: Survey data will be collected at the end of the intervention up to 30 minutes post intervention.

Secondary outcomes (1)
  1. The number of subjects reporting the intervention was well facilitated.

    This will be measured on a Likert scale where 0 is strongly disagree and 5 is strongly agree

    Measured: Survey data will be collected at the end of the intervention up to 30 minutes post intervention.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Jun 2025
  2. Study start1 Sep 2027 (estimated)
  3. Primary completion30 Apr 2028 (estimated)
  4. Study completion30 Apr 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07018609
Sponsor's protocol ID
Study00026654
Status last verified
Jun 2026
First submitted
4 Jun 2025
Last updated
5 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Zen Den Experience and Music Therapy Experience in people with Burn Out and Nurses, run by Milton S. Hershey Medical Center.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 5 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact ERIC R MESSNER, PhD (7175318348, emessner@pennstatehealth.psu.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The number of subjects who state preference for having long-term access to the intervention. (time frame: Survey data will be collected at the end of the intervention up to 30 minutes post intervention.). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Jun 2026.

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