Chronic fatigue syndrome. Postviral fatigue syndrome
Conditions
Interventions
Intervention 1: Intervention group: Intervention group: In this study, the root extract extracted in hydroalcoholic form is prepared by Barij-Essance company in 500 mg capsules and will be given to th
Sponsors
Kashan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Have criteria for chronic fatigue syndrome. 20 to 50 years old. A nurse working in a hospital. Willingness to participate in the study
Exclusion criteria
Exclusion criteria: Unwillingness to continue participating in the study Not taking medicine for 4 consecutive days Lack of access to samples receiving anticoagulants (warfarin-aspirin-coumadin ) Blood pressure drop (systole less than 100 and diastole less than 60) during study continuously or intermittently during the day
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Chronic fatigue syndrome. Timepoint: At the beginning of the study (before the start of the intervention), the end of the intervention, one month after the end of the intervention. Method of measurement: DePaul Symptom Questionnaire - Short Form (DSQ-SF). | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety. Timepoint: At the beginning of the study (before the start of the intervention), the end of the intervention, one month after the end of the intervention. Method of measurement: Beck Anxiety Inventory.;Sleep quality. Timepoint: At the beginning of the study (before the start of the intervention), the end of the intervention, one month after the end of the intervention. Method of measurement: Pittsburgh Sleep Quality Index. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Ismail Azizi-Fini
Kashan University of Medical Sciences
Outcome results
None listed