Compassion Fatigue
Conditions
Interventions
This is an experimental study, of the randomized controlled clinical trial type, with parallel groups, double blind, with three arms. The materials and methods for the RCT will follow the provisions o
Wrist stitch and cheek stitch. Control group - waiting list: 16 nursing professionals who meet the inclusion criteria will be kept on the waiting list for later comparison of results.
E02.190.204
E02.190.044.133
Sponsors
Hospital Universitário Júlio Muller
Hospital Universitário Júlio Muller
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: nursing professionals with at least 6 months of practical experience; who work in sectors that provide direct care to patients; that you have answered all the questions in the questionnaires; who have available time to participate in the stages of the research, and who agree to participate in the research by signing the Free and Informed Consent Term
Exclusion criteria
Exclusion criteria: having a previously diagnosed severe psychiatric disorder in continuous use of psychotropic medications; being pregnant, on vacation, or on leave during the intervention period; act only in administrative functions; presenting skin lesions, infection, inflammation or injury to the ear; allergic to adhesive tape in the pavilion; excessive oiliness in the ear; use a hearing aid; use steroidal anti-inflammatory drugs or opioid analgesics; to have coagulation disorders, or to use anticoagulants
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to observe a decrease in the general average of compassion fatigue, measured using the ProQol-IV scale, in the real auriculotherapy group, at the end of the 8 sessions of auriculotherapy and 15 days after the end of the sessions. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to observe a decrease in the general averages of depression, anxiety and stress, measured by the DASS-21 scale, at the end of the 8 sessions of auriculotherapy and after 15 days of the end of the sessions. | — |
Countries
Brazil
Contacts
Public ContactMargani Weis
Universidade Federal de Mato Grosso
Outcome results
None listed