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Online Yoga for Managing Covid-19 Induced Psychological Problems

Online Yoga Intervention as Tertiary Prevention of Psychological Comorbidities of Covid-19 Survivors - OYITPPCCOVID

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033793
Enrollment
66
Registered
2021-05-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: F063- Mood disorder due to known physiological condition

Interventions

Intervention1: Online Yoga Intervention: 22 participants are expected to go through one-month online yoga classes (5 classes/week) by covering the yogic practices as mentioned in yoga protocol. Asanas

Sponsors

Patnajli Ayurved Hospital
Lead Sponsor

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

MeasureTime 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

MeasureTime 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

Public ContactDr Velan

University of Patanjali

rbap@uop.edu.in9634510540

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026