Ayurvedic intervention for stress in IT professionals
- Conditions
- Health Condition 1: F438- Other reactions to severe stress
- Registration Number
- CTRI/2019/08/020798
- Lead Sponsor
- CCRAS MINISTRY OF AYUSH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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.
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Outcome Measure <br/ ><br>- Change in Occupational Stress Index (OSI) score <br/ ><br>Timepoint: 3 years - study duration <br/ ><br>90 days - Intervention period
- Secondary Outcome Measures
Name Time Method Secondary Outcome Measure <br/ ><br>-Changes in the scores of WHO Well- Being Index (1998 version) <br/ ><br>-Changes in the scores of ManasaBhavaPareeksha <br/ ><br>Timepoint: 3 years - study duration <br/ ><br>90 days - Intervention period