anxiety
Conditions
Interventions
Experimental group:Tanxiang Prescription was used as intervention method for 28 days, and two health education sessions were conducted
Control group: two health education sessions were conducted
Sponsors
Zhejiang Chinese Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 27 Years
Inclusion criteria
Inclusion criteria: 1. Meet the diagnostic criteria for anxiety. 2. Female college students, aged 18-35 years old. 3. The self-rating anxiety Scale score was evaluated as mild to moderate anxiety. 4. Sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Received medication (anti-anxiety medication) in the previous 3 months. 2. Patients with other mental disorders, such as unstable periodic mood disorder, bipolar disorder or suicidal ideation, etc. 3. Complicated with serious primary diseases such as cardiovascular, cerebrovascular, liver, kidney and hematopoietic system. 4. Patients who were allergic to any component of the study drug. 5. Pregnant and lactating women. 6, patients who are participating in clinical trials of other drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Self-Rating Anxiety Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Self-Rating Depression Scale;Pittsburgh Sleep Quality Index; | — |
Countries
China
Contacts
Public ContactXiaqiu Wu
College of Public Health, Zhejiang Chinese Medical University
Outcome results
None listed