Moral sensitivity and moral distress of operating room personnel.
Conditions
Interventions
Intervention 1: Intervention group: pre-prepared educational materials that include professional ethics training in the form of mobile phone software, which will be approved by the professors of the n
It will be provided to the intervention group and it will be installed on their mobile phone or tablet (equipped with Android operating system) and how to work with the software will be explained to t
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Having at least 6 months of experience in the operating room Having at least an associate's degree in the fields of operating room, intelligence and nursing Be able to use mobile software and their smartphone should be equipped with Android operating system Absence of mental disorder and non-use of antidepressants or drugs related to mental disorders by self-reporting method by personnel
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Moral sensitivity is the score given by respondents to the 25 item questions of Lutzen et al.'s Modified Moral Sensitivity Questionnaire (MMSQ). The score range of this questionnaire will be between 0 and 100, which is scored based on a 5-point Likert scale. The highest score is 100 and the lowest score is zero. Therefore, if the total score of each sample is between 0 and 50, it is considered as having low moral sensitivity, 50 to 75 as medium sensitivity, and 75 to 100 as high moral sensitivity. Moral distress will be used from the revised 21item questionnaire of Corley 2001, which is scored on a 5-point Likert scale. The minimum score is 0 and the maximum score is 336, a higher score indicates more moral distress of the person. Timepoint: The pre-test phase will be held at the beginning of the study for all the participants in the study, and the moral sensitivity and moral distress questionnaires will be provided to the participants of both groups as a pre-test. The intervention period will be 4 weeks. After the completion of the intervention, moral sensitivity and moral distress questionnaires will be collected again immediately and 2 months after the end of the intervention between the two intervention and control groups, distribution and data will be collected. Method of measurement: Moral sensitivity is the score given by the respondents to the 25 item questions of Lutzen et al.'s adjusted moral sensitivity questionnaire. Moral distress will be used from the revised 21 item questionnaire of Corley 2001, which is scored on a 5-point Likert scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAbbas Rezaee
Shiraz University of Medical Sciences
Outcome results
None listed