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Burnout, ProfessionalEMOCARENCT06882226

Evaluation of the Emotional Burden of the Nurse

An observational study of Burnout, Professional, run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS.

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

Asses the emotional burden on nursing staff and how much they are at risk for burnout. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Burnout, Professional
What is being tested?
Maslach burnout inventory
How many people
20 participants
Where
No sites listed yet
Study dates
Mar 2025to Apr 2025
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
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Nurse attached to uoc 1E hematology and TCSE and uoc 5E geriatric hematology and rare diseases.

Who may be able to join

  • Nursing personnel afferent to the OU of hematology and stem cell transplantation hematopoietic and the uoc geriatric hematology and rare hemapathies with more than 2 years of experience in the above departments.
  • Signature of informed consent.
  • Ability to understand and complete.

Who cannot join

  • Nursing staff not belonging to the departments of hematology
  • Failure to sign informed consent

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: Evaluation of the Emotional Burden of the Nurse in Onco-hematology

Asses the emotional burden on nursing staff and how much they are at risk for burnout.

Read the detailed description

The study involves the administration of a questionnaire paper questionnaire (maslach burnout scale) in the presence.

Being tested
Maslach burnout inventory
Medical subject headings
Burnout, Professional

What participants receive

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

  • Maslach burnout inventoryOther

    Assessing the emotional burden on nursing staff

What is being measured

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

  1. Assessment of emotional burden on nursing staff

    Maslach burnout scale

    Measured: 1 month

Timeline

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

  1. First posted18 Mar 2025
  2. Study startMar 2025 (estimated)
  3. Primary completionMar 2025 (estimated)
  4. Study completionApr 2025 (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
Prospective
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06882226
Sponsor's protocol ID
7360
Acronym
EMOCARE
Status last verified
Mar 2025
First submitted
12 Mar 2025
Last updated
18 Mar 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Burnout, Professional, run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS.

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 3 inclusion and 2 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 18 Mar 2025. 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 Fabio Lamberti (0630154132, fabio.lamberti@policlinicogemelli.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assessment of emotional burden on nursing staff (time frame: 1 month). 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 18 Mar 2025.

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