Jasmine impact on the levels of anxiety and cortisol exposure of patients to the operating room
Not Applicable
- Conditions
- Anxiety.Generalized anxiety disorder.
- Registration Number
- IRCT2015072510325N4
- Lead Sponsor
- Golestan University of Medical Sciences Vice Chancellor for research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 84
Inclusion Criteria
65-15 years old, patients who are candidate for laparotomy without a history of mental illness and no signs of trauma to the brain, alert to place, time and self orientation, no history of allergy to plants, no disorder in smell, having ability to read and response to questionnaire items, no history of using steroid during 3 months ago, or those disease that increase the level of blood Cortisol.
Exclusion criteria:
Patient's intolerance due to Jasmine extraction, patient transmission before the intervention, the patient withdraw from the study, and the patients with anxiety or depression disorders.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ??Anxiety. Timepoint: Before and one hour (60 minutes) after intervention the anxiety will be measured. Method of measurement: Spielberger questionnaire.;Blood Cortisol. Timepoint: Before and one hour after intervention the subjects' blood samples will be taken and the level of Cortisol will be measured. Method of measurement: Using ELISA monitors Cortisol IBl kit.
- Secondary Outcome Measures
Name Time Method Vital sign. Timepoint: Before and one hour after intervention. Method of measurement: Blood pressure of the subjects will be measured before and after the intervention by a Manometer ALPK2 that was manufactured by Japan. The subjects' pulse rate and respiratory rate will be counted.