Anxiety level. Anxiety disorder, unspecified
Conditions
Interventions
Intervention 1: Intervention group: The intervention group is given tea containing 100 mg of saffron and 100 ml of water for 40 days. At the beginning of the study, demographic questionnaire and Spiel
Sponsors
Arak University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahbobeh Sajadi
Arak University of Medical Sciences
Outcome results
None listed