Tele yoga v/s in-person yoga for persons with Common Mental Health Disorder
- Conditions
- Other nonpsychotic mental disorders,
- Registration Number
- CTRI/2022/07/044479
- Lead Sponsor
- DST Science and Technology of Yoga and Meditation DST SATYAM India
- Brief Summary
The primary objective of project is to compare the effect of Virtual Yoga and in-person yoga sessions in reducing the depressions and anxiety symptoms in participants. The secondary objectives are to effect of Virtual Yoga and in-person yoga sessions in improving the well-being, quality of life in participants. The total (n=60) patients with Common mental health Disorders will recruited from OPD of NIMHANS Bangalore. This patient will be randomized through the computer generated numbers and assigned into any two groups each (Virtual yoga=30) and (In-person-Yoga), as per the code. The inclusion criteria of is both gender both male and female participants with age group of 18-60 years will taken for the study. Patient diagnosed with Common Mental disorders diagnosed according to ICD-10 (Categories F32.0, F40, F41, F43, F44 and F45) and with less clinical global inventory (CGI) Score <= 4. The patients should also able to read, write and working knowledge of English. The patient should have the availability of high-speed internet access (512 Mbps and above) and high definition powerful web-camera facility at the therapist site and subject’s house. The *Exclusion Criteria is that patient should not have* Obsessive Compulsive Disorder (F 42) *or* Severe Depression with or without psychotic symptoms (F 32.3 onwards, and the participants who are already practicing yoga regularly for the past 3 months. Post recruitment, the participants will be explained the purpose of the study and their written informed consent will be obtained. The SRF who is conducting the assessments would hence be unaware of the group status of the participants. The validated Yoga for Psychiatric Disorders’ Module will be provided for 10 supervised session for 30-40 minutes per day over a period of one month
The assessments would be conducted at Baseline (Day 0), Post Intervention (Day 30), Day 60 (1st Follow-up) and Day 90 (2nd Follow-up). At each follow-up apart from the assessments, the participants would be provided a booster yoga session and their adherence of yoga practice at home would be checked for the previous month. The clinical assessments included in the projects are socio-demographic details and Hamilton Anxiety Rating Scale (HAM-A) : 14 and Hamilton Depression Rating Scale (HDRS): 17 to measures the anxiety and depression. The other assessment such as Edinburgh Mental Wellbeing Scale: 14 items, Quality of Life: (WHOQOL Brief) 26 items, Virtual Yoga Trainers Assessment (VYTA) Qualitative Feedback form. The yoga assessment will be conducted by yoga therapist based on Yoga performance Assessment Scale (YPA): Visual analog scale (VAS). The socio-demographic characteristics will be analyzed using the chi-square and t test. Based on the normality of the data, the differences among groups across timeline from baseline to the end of three months will be analyzed using the RMANOVA. The group differences at a particular follow-up will be analyzed using Independent Sample t test. Manual Content Analysis will be used to analyze the qualitative feedback data.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 60
- Inclusion criteria 1.
- Common mental health disorder diagnosed to ICD-10(Categories F32.0, F40,F41,F43,F44 and F45).
- Clinical Global Inventory (CGI)score less than or equal to 4 3.
- Availability of high internet access (512 Mbps and above) and high definition powerful web-camera facility at the therapist site and subjects house 4.
- able to read, write and working knowledge of english.
Exclusion Criteria: 1)Obsessive Compulsive Disorder (F 42) 2)Severe Depression with or without psychotic symptoms (F 32.3 onwards) 3)Participants who are already practicing yoga regularly for the past 3 months.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Depressions and anxiety symptoms Baseline, Day 30, Day 60 and Day 90
- Secondary Outcome Measures
Name Time Method Well-being Baseline, Day 30, Day 60 and Day 90 Improve quality of life Baseline, Day 30, Day 60 and Day 90
Trial Locations
- Locations (1)
Room no. 34, (OPD), Psychiatry, National Institute of Mental Health and Neurosciences
🇮🇳Bangalore, KARNATAKA, India
Room no. 34, (OPD), Psychiatry, National Institute of Mental Health and Neurosciences🇮🇳Bangalore, KARNATAKA, IndiaDr Aarti JagannathanPrincipal investigator9448150690jaganaarti@gmail.com