A randomized double blind placebo controlled clinical trial on Ayurvedic intervention in the management of Occupational stress among I T professionals - AYUSH-SR

CCRAS MINISTRY OF AYUSH0 个研究点目标入组 0 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•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.

发起方

CCRAS MINISTRY OF AYUSH