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A clinical trial to study the effect on Mental Health of Brahmi Oil Head massage in Healthy College Students.

Evaluation of Mental Health Promotive Effect Of Brahmi Taila Shiroabhyanga in healthy College Students.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052633
Enrollment
30
Registered
2023-05-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

None listed

Interventions

None listed

Sponsors

Dr.Tripuri Takalkar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Newly admitted Ist year students to B. A. M. S. course 2) Either Sex

Exclusion criteria

Exclusion criteria: 1) Participants contra-indicated for Shiroabhyanga such as Ajeerna, Nava Jwara, etc. 2) Participants on anti-depressants, anxiolytic medications, or sedatives, etc. i.e., those suffering from severe Mental illness. 3) Participants of head trauma. 4) Participants suffering from any systemic or metabolic disorders. 5) Participants undergoing detox treatment for addiction. 6) Participants showing symptoms of Samaavastha such as Gaurava, Aalasya, etc.

Design outcomes

Primary

MeasureTime frame
Participants practicing Shiroabhyanga with Brahmi Taila are expected to show 1. Lower levels of ISMA score meaning they are least likely to suffer from stress-related illness. 2. Lower HAM-A score, indicating lesser severity of anxiety. 3. Lower PSQI score, which can be interpreted as overall improved sleep quality.Timepoint: Baseline, 7th, 14th & 21st day. and Post up follow up on 30th day.

Secondary

MeasureTime frame
Participants practicing Shiroabhyanga with Brahmi Taila are expected to show 1. Lower levels of ISMA score meaning they are least likely to suffer from stress-related illness. 2. Lower HAM-A score, indicating lesser severity of anxiety. 3. Lower PSQI score, which can be interpreted as overall improved sleep quality. These can provide a safer, cost effective alternative to the present conventional treatment, which can be useful in a country like India.Timepoint: Baseline, 7th, 14th & 21st day. and Post up follow up on 30th day.

Countries

India

Contacts

Public ContactDrSudeep Menon

Bharati Vidyapeeth (Deemed to Be University)

sudeep.menon@bharatividyapeeth.edu8007283293

Outcome results

None listed

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