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Developing, Validating, and Assessing the Feasibility of a Satvavajaya Chikitsa Module in Vishada (Mild to moderate depression).

Development,validation and feasibility of Satvavajaya Chikitsa module for Vishada. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072619
Enrollment
12
Registered
2024-08-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: F330- Major depressive disorder, recurrent, mild Health Condition 2: F331- Major depressive disorder, recurrent, moderate Health Condition 3: F320- Major depressive disorder, singleepisode, mild Health Condition 4: F321- Major depressive disorder, singleepisode, moderate

Interventions

Intervention1: Satvavajaya Chikitsa: Satvavajaya Chikitsa is one among the trividha chikitsa defined in Ayurveda. Satvavajaya Chikitsa has 5 key components -Jnana, Vijnana, Dhairya, Smruti, and Samadh
2) Problem assessment -- Vijnana and Jnana
3) Goal setting - Vijnana and Jnana
4) Intervention and observation - Vijnana, Dhairya, Smruti, Samadhi
5) Termination and Post assessment - Reinforcement of Dhairya and samadhi. Control Intervention1: NIL: NIL

Sponsors

Dr Divya T
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients who satisfy the clinical diagnostic criteria of Vishada who are on stable medication. 2) Mild and moderate depression diagnosed according to ICD-10. HAM – D (score 8-23)

Exclusion criteria

Exclusion criteria: 1) Patients currently undergoing any kind of structured psychotherapy. 2) Patients with attempts of deliberate self-harm in the last 1 month. 3) Patients with Kaphaja Unmada and other Manasa rogas. 4) Patients with HAM – D (score more than or equal to 24), substance abuse, and other major psychiatric illnesses.

Design outcomes

Primary

MeasureTime frame
Feasibility testingTimepoint: Pre-assessment at Baseline Post assessment after 6 weeks of intervention.

Secondary

MeasureTime frame
Symptoms reductionTimepoint: Pre-assessment at Baseline Post assessment after 6 weeks of intervention.

Countries

India

Contacts

Public ContactDr Kishore Kumar R

National Institute of Mental Health and Neurosciences (NIMHANS)

vddivyat@gmail.com8550006252

Outcome results

None listed

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