Health Condition 1: F063- Mood disorder due to known physiological condition
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)An email address, an internet-connected computer with camera and sound system/ tablet or 4G and/or Wi-Fi enabled Smartphone (running Google chrome). 2)Symptomatic medical history of at least 2 month back and BDI Score=10 or Hamilton Anxiety Scale Score greater than or equal to 17. 3)Faith on mind body practices and Ayurveda, no involvement in other exercises and interest for voluntary participation in the study.
Exclusion criteria
Exclusion criteria: Participants with medical health issues as under before the onset of clinical symptoms of Covid-19 infection: Neurological, hypertension, diabetes mellitus, Cardiovascular disease, renal complications, liver disorders, locomotors disabilities, glaucoma, hernia, ulcers of the stomach or intestine, recent abdominal or spinal surgery, pregnancy/lactating phase, addictive behaviors (smoking, alcoholism, tobacco chewing) and age below 15 and above 60 years.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1)Proposed OYI with and without herbal concoction is expected to improve the PTSD, Anxiety, Depression and Quality of Life of COVID-19 survivors in Experimental groups as compared to the controls. 2)If this OYI protocol proves to be effective, then it may be a good option for over millions global COVID-19 survivors to overcome comorbidities, boost immunity and restore health. Timepoint: Staff Recruitment & training: 01-15 July 2021 Recruitment of Participants, Randomization: 15 July- 15 August 2021 Baseline scoring of instruments: 15-30 August 2021 (4 weeks) Final scoring of instruments after intervention: 01-05 September 2021 (one week) Data Entry and Analysis: 15-30 September 2021 Compilation of annual report: October-November 2021 | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety, Post Traumatic Stress Disorder and Quality of Life Timepoint: Baseline and Post Intervention Measurement of Secondary Outcome Variables will be completed in 4 weeks and one week respectively | — |
Countries
India
Contacts
University of Patanjali