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Burnout, Healthcare WorkersBSAFENCT07773168

Burnout and Safety Assessment in Home Hospital Versus Brick-and-Mortar Hospital

An observational study of Burnout, Healthcare Workers and Workplace Violence, run by Brigham and Women's Hospital at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The goal of this observational study is to learn about burnout and workplace violence among frontline clinicians working in Home Hospital programs compared with traditional brick-and-mortar hospitals. The main questions it aims to answer are: 1. Read more about this study

Who is it for?
Ages 18 years and older
How many people
500 participants
Where
1 siteUnited States
Study dates
4 Jul 2026to Jul 2027
Phase
Observational
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
  • No healthy volunteers
  • Adult, Older adult

Study population: Frontline clinicians who provide at least 25% of their clinical effort in either a Home Hospital program or a traditional brick-and-mortar inpatient hospital setting (including nurses, physicians, advanced practice providers, paramedics, social workers, physical therapists, occupational therapists, and speech therapists.)

Who may be able to join

None listed.

Who cannot join

  • None

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

David M Levine, MD, MPH, MA contact

617-732-7063

dmlevine@bwh.harvard.edu

Fernando Chavarria, MD, MSc contact

857-307-2673

fchavarria@bwh.harvard.edu

United States1 site, 1 recruiting
  • Brigham and Women's Hospital

    Boston, Massachusetts, 02120

    David M Levine, MD, MPH, MA

    Recruiting

Other trials in United States

About this study

Official title: Burnout and Safety Assessment for Frontline Clinical Employees in Home Hospital and Brick-and-Mortar Hospital

The goal of this observational study is to learn about burnout and workplace violence among frontline clinicians working in Home Hospital programs compared with traditional brick-and-mortar hospitals. The main questions it aims to answer are:

  1. Do Home Hospital clinicians experience different levels of burnout than clinicians working in traditional inpatient hospital settings?
  2. Do Home Hospital clinicians experience different rates of workplace violence and harassment than clinicians working in traditional inpatient hospital settings?
Read more

Researchers will compare clinicians working primarily in Home Hospital settings with clinicians working primarily in brick-and-mortar hospitals to assess differences in burnout, workplace safety, and work experience.

Participants will:

  • Complete a one-time anonymous online survey through REDCap.
  • Answer questions about their demographic and professional background.
  • Complete validated questionnaires assessing burnout, workplace safety culture, and experiences with workplace violence or harassment.
  • Provide optional free-text feedback about their work experience.
Medical subject headings
Burnout, Psychological

What participants receive

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

Study groups in NCT07773168
Study groupRoleWhat they receive
Home hospital cliniciansNot described
Brick-and-mortar hospital cliniciansNot described

What is being measured

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

  1. Mini Z Burnout Score

    Burnout will be assessed using the single-item burnout measure from the Mini Z. Responses range from 1 to 5, with higher scores indicating greater burnout.

    Measured: Baseline (at time of survey completion; single time point)

  2. % reporting physical or verbal violence at work

    Percentage of participants who report ever experiencing physical or verbal violence while working in their particular unit. Participants will indicate whether they have experienced physical violence, verbal violence, or both in that unit. The outcome will be reported as the percentage of participants reporting any physical or verbal violence, with a higher percentage indicating a worse outcome.

    Measured: Baseline (at time of survey completion; single time point)

Secondary outcomes (1)
  1. Net promoter score

    Net Promoter Score measures participants' likelihood of recommending the program or service. Participants rate their likelihood of recommending it from 0 (not at all likely) to 10 (extremely likely). Respondents are classified as detractors (0-6), passives (7-8), or promoters (9-10). Net Promoter Score is calculated as the percentage of promoters minus the percentage of detractors and ranges from -100 to 100. Higher scores indicate a better outcome.

    Measured: Baseline (at time of survey completion; single time point)

Timeline

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

  1. First posted19 Aug 2026
  2. Study start4 Jul 2026
  3. Primary completionDec 2026 (estimated)
  4. Study completionJul 2027 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07773168
Sponsor's protocol ID
2026P001405
Acronym
BSAFE
Status last verified
Jul 2026
First submitted
12 Aug 2026
Last updated
20 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Burnout, Healthcare Workers and Workplace Violence, run by Brigham and Women's Hospital at 1 site in United States.

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 0 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: looking for participants now, as of the sponsor's last update on 20 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

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 David M Levine, MD, MPH, MA (617-732-7063, dmlevine@bwh.harvard.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mini Z Burnout Score (time frame: Baseline (at time of survey completion; single time point)). The study lists 2 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 20 Aug 2026.

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