Menu
Not yet recruiting NCT06882226

Evaluation of the Emotional Burden of the Nurse

Observational Burnout, Professional

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Maslach burnout inventory.
Who it may be relevant to
Registry conditions: Burnout, Professional. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

Detailed description

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

Interventions

  • Other Maslach burnout inventory
    Assessing the emotional burden on nursing staff

Primary outcome measures

  • Assessment of emotional burden on nursing staff [Time frame: 1 month]

Eligibility criteria

Inclusion criteria

  • 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.

Exclusion criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06882226 · 7360

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗