Health Condition 1: F438- Other reactions to severe stress
Conditions
Interventions
Intervention1: AYUSH SR - A coded drug: 1. AYUSH - SR(In tablet form)
Dose 500 mg X 2 tab b i d
Dosage form Tablet
Route of Administration Oral
Time of Administration Twice a day after fo
Sponsors
CCRAS MINISTRY OF AYUSH
Eligibility
Inclusion criteria
Inclusion criteria: 1. Software professionals with a work experience of more than one year 2. Subjects screened with OSI (Occupational Stress Index) (Manual of Occupational Stress Index, Dr. A. K Srivastava & Dr. A.P Singh (1982), Department of Psychology, BHU) and those who scored above 46 areincluded. 3. Subjects who are willing to participate in the clinical trial and signing the consent form. 4. Subjects in the age group 25 - 40 years irrespective of gender and socioeconomic status. 5. Subjects fulfilling the diagnostic criteria.
Exclusion criteria
Exclusion criteria: 1. Patients suffering from other psychiatric disorders and using anti psychiatric therapy 2. Subjects with history of Alcoholism and substance abuse 3. Patients with Hypothyroidism and Hyperthyroidism 4. Patients with concurrent serious Hepatic Dysfunction (defined as AST and/or ALT > 2 times of the upper normal limit) or Renal Dysfunction (defined as S. creatinine > 1.2mg/dl), uncontrolled Pulmonary Dysfunction (asthmatic and COPD patients) or other concurrent severe disease. 5. Diabetic patients with HbA1c value above 8 6. Patients whose blood pressure systolic above 160 mm of Hg and diastolic more than 100 mm of Hg 7. Women who are planning to conceive, Pregnant or lactating woman. 8. H/o hypersensitivity to any of the trial drugs or their ingredients. 9. Patients who have completed participation in any other clinical trial during the past 3 months. 10. Any other condition which the investigator thinks may jeopardize the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary Outcome Measure - Change in Occupational Stress Index (OSI) score Timepoint: 3 years - study duration 90 days - Intervention period | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary Outcome Measure - Changes in the scores of WHO Well- Being Index (1998 version) - Changes in the scores of ManasaBhavaPareeksha Timepoint: 3 years - study duration 90 days - Intervention period | — |
Countries
India
Contacts
Public ContactG V RAMANA
CCRAS MINISTRY OF AYUSH
Outcome results
None listed