Nursing Alarm Fatigue. Diagnostic and monitoring general hospital and personal-use devices associated with adverse incidents
Conditions
Interventions
Intervention 1: Intervention Group: First, the informed consent form will be completed. In the next stage, all participants in the intervention group will complete the pre-test. Based on the results o
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
23 Years to 60 Years
Inclusion criteria
Inclusion criteria: Willingness to participate in the study Be a permanent nurse in an adult intensive care unit Have a minimum of 6 months of work experience in an adult intensive care unit No self-reported history of chronic mental illness No self-reported history of disabling chronic physical illness Having the ability to express feelings and experiences
Exclusion criteria
Exclusion criteria: Participation in psychotherapy programs or receipt of psychological counseling within the past six months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nursing Alarm Fatigue. Timepoint: Before the intervention, immediately after, and two months following the implementation of the intervention. Method of measurement: Alert fatigue Questionnaire developed by Tarabizadeh et al. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohsen Ranjbar
Shiraz University of Medical Sciences
Outcome results
None listed