Evaluation of the effect of crocus sativus tea on anxiety level
Not Applicable
- Conditions
- F41.9Anxiety level.Anxiety disorder, unspecified
- Registration Number
- IRCT20210501051142N4
- Lead Sponsor
- Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 68
Inclusion Criteria
Nurses who attend the ward only for 175 hours per month (mandatory hours).
Not taking any sedative and anti-anxiety drugs
Exclusion Criteria
Unwillingness to participate in the study
Allergic to saffron
Complications caused by the consumption of saffron
The presence of any underlying disease
Pregnancy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anxiety rate. Timepoint: Before the intervention and 40 days after the start of the first intervention, the anxiety level of each patient is measured. Method of measurement: At the beginning and end of the study, the demographic questionnaire and the Spiel Berger questionnaire were completed by the nurses of both groups and based on this, the anxiety level of nurses is determined.
- Secondary Outcome Measures
Name Time Method