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"Reducing Office Stress with Til Taila Abhyanga: An Evalution Study"

Evaluation of Efficacy of Tila Taila Abhyanga in Occupational Stress among Office Workers - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085445
Enrollment
40
Registered
2025-04-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: F419- Anxiety disorder, unspecified Health Condition 2: F419- Anxiety disorder, unspecified

Interventions

None listed

Sponsors

Rajiv Gandhi Government Postgraduate Ayurvedic College and Hospital Paprola 176115 india
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Individuals willing for trial. 2.Individuals having age between 25 to 60 years. 3.Office workers with scale score ranging from 31 to 45. 4.Participants must be employed as office workers, with defined job roles that involve desk-based work, prolonged sitting.

Exclusion criteria

Exclusion criteria: 1.Individuals unwilling for trial . 2.Individuals below 25 years and above 60 years. 3.Office workers with scale scores less than 31 or more than 45. 4.Individuals with chronic medical conditions such as cardiovascular diseases, diabetes, or autoimmune disorders etc. 5.Individuals who have experienced recent trauma, injuries, or surgeries. 6.Individuals who regularly engage in other relaxation techniques such as yoga, meditation, or acupuncture. 7.Individuals who are currently taking medications known to significantly affect stress levels such as sedatives, hypnotics,anxiolytics, antidepressants and beta blockers. 8.Pregnant and Lactating women.

Design outcomes

Primary

MeasureTime frame
Benefits of Til Taila Abhyanga in the reduction of stress among office going workersTimepoint: 4 weeks

Secondary

MeasureTime frame
Reduction in symptoms of Occupational stress such as Kleshsaho,Sharira-Dridhta,Sutwaka,VyayamsansahamaTimepoint: Follow up after 28 days and then after one month of completion of trial

Countries

India

Contacts

Public ContactDr Ankush Jagota

Rajiv Gandhi Government Postgraduate Ayuvedic College and Hospital Paprola

shalinidoctor48@gmail.com8628074932

Outcome results

None listed

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