Comparison of physiological indices and students' fatigue index after cardiopulmonary resuscitation with and without personal protective equipment..
Conditions
Interventions
Intervention 1: "Intervention group:" In this group, 20 nursing intern students enter the clinical skills center of the nursing faculty in the form of groups of two. In the beginning, physiological in
Sponsors
Jahrom University of Medical Sciences
Eligibility
Sex/Gender
All
Age
21 Years to 30 Years
Inclusion criteria
Inclusion criteria: No history of respiratory diseases and heart disorders Body mass index 18 to 30 Not participating in regular and professional sports activities Passing the theoretical and practical unit of cardiopulmonary resuscitation in accordance with the educational curriculum of the field of nursing Resting heart rate greater than 50 beats per minute or less than 120 beats per minute At rest, oxygen saturation is more than 95% Resting breathing rate should be more than 10 or less than 20 beats per minute Do not have Covid 19 disease or have no symptoms at the time of the study Do not recover from Covid 19 Absence of pregnancy or menstruation in women at the time of the study Age 21 to 30 years
Exclusion criteria
Exclusion criteria: Students who did not pass the 7th nursing semester. Lack of access to participant prior to randomization
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fatigue score in Borg cr10 questionnaire. Timepoint: At the beginning of the study (before the start of cardiopulmonary resuscitation) and 12 minutes after the start of resuscitation in both intervention and control groups. Method of measurement: Pressure Borg CR10 Perception Scale Questionnaire.;Blood pressure score in mm Hg. Timepoint: At the beginning of the study (before the start of cardiopulmonary resuscitation) and 12 minutes after the start of resuscitation in both intervention and control groups. Method of measurement: Tensval digital blood pressure checker comfort model.;Arterial blood oxygen saturation percentage. Timepoint: At the beginning of the study (before the start of cardiopulmonary resuscitation) and 12 minutes after the start of resuscitation in both intervention and control groups. Method of measurement: New model blood oxygen check machine (onix Vantage).;The number of heartbeats per minute. Timepoint: At the beginning of the study (before the start of cardiopulmonary resuscitation) and 12 minutes after the start of resuscitation in both intervention and control groups. Method of measurement: Tensval digital blood pressure checker comfort model.;Degree of oral fever. Timepoint: At the beginning of the study (before the start of cardiopulmonary resuscitation) and 12 minutes after the start of resuscitation in both intervention and control groups. Method of measurement: Imperial digital thermometer model 301. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSaharTavan
Jahrom University of Medical Sciences
Outcome results
None listed