Condition 1: Sleep quality. Condition 2: Anxiety. Condition 3: Depression. Sleep disorders Generalized anxiety disorder Major depressive disorder, single episode
Conditions
Interventions
Intervention 1: Intervention group: Elderly individuals receive one capsule containing 750 mg of rosemary (the drug is safe at this dose) every evening for 4 weeks. Intervention 2: Control group: Elde
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Age
65 Years to No maximum
Inclusion criteria
Inclusion criteria: People = 65 years of age residing in nursing homes
Exclusion criteria
Exclusion criteria: People with rosemary allergies People taking sleeping pills, anti-anxiety medications, and sedatives
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Score of sleep quality. Timepoint: At the beginning (before the intervention) and 4 weeks after the start of rosemary consumption. Method of measurement: Pittsburgh Sleep Quality Inventory (PSQI).;Anxiety score. Timepoint: At the beginning (before the intervention) and 4 weeks after the start of rosemary consumption. Method of measurement: Hospital Anxiety and Depression Scale (HADS).;Depression score. Timepoint: At the beginning (before the intervention) and 4 weeks after the start of rosemary consumption. Method of measurement: Hospital Anxiety and Depression Scale (HADS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Dabaghzadeh
Kerman University of Medical Sciences
Outcome results
None listed