NCT06882226

Brief Summary

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

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Mar 2025

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2025

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2025

Completed
11 days until next milestone

First Submitted

Initial submission to the registry

March 12, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 18, 2025

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2025

Completed
Last Updated

March 18, 2025

Status Verified

March 1, 2025

Enrollment Period

Same day

First QC Date

March 12, 2025

Last Update Submit

March 12, 2025

Conditions

Burnout, Professional

Outcome Measures

Primary Outcomes (1)

  • Assessment of emotional burden on nursing staff

    Maslach burnout scale

    1 month

Interventions

Maslach burnout inventoryOTHER

Assessing the emotional burden on nursing staff

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

  • 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.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Burnout, Professional

Interventions

Maslach Burnout Inventory

Condition Hierarchy (Ancestors)

Occupational StressOccupational DiseasesBurnout, PsychologicalStress, PsychologicalBehavioral SymptomsBehavior

Study Officials

  • Fabio Lamberti

    FPG

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Fabio Lamberti

CONTACT

0630154132fabio.lamberti@policlinicogemelli.it

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 12, 2025

First Posted

March 18, 2025

Study Start

March 1, 2025

Primary Completion

March 1, 2025

Study Completion

April 1, 2025

Last Updated

March 18, 2025

Record last verified: 2025-03