Designing and Testing a Stress Relief Program Before Operation

Designing, Validation, and Feasibility of a Yoga-Based Intervention for Pre Operative Stress - NA

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/07/091815

Enrollment

Registered

2025-07-28

Start date

Unknown

Completion date

Unknown

Last updated

2025-08-18

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

Conditions

Health Condition 1: F06- Other mental disorders due to known physiological condition

Interventions

Intervention1: Two Arm Compare Study: Daily 25-minute sessions (20-22 days pre-surgery) including Om Chanting, asanas (Vajarasana, Makrasana), pranayama (Bhramari ), and mindfulness meditation (Yoga-N

Eligibility

Inclusion criteria

Inclusion criteria: 1. People who must undergo surgery. 2. For people who can read at least as well as a sixth grader. 3. Both genders. 4. Willing to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Individuals with a history of neurologic disease. 2. Known case of psychiatric disease. 3. Those who are unable to perform yogic practices 4. Emergency surgery. 5. Known cases of Renal failure, Paralysis, Parkinson s disease, severe Anemia, and Malignancy, Pregnant and Lactating females, Syphilis, AIDS, Leprosy, and Bleeding disorder. Those who are unable to perform yogic practices.

Design outcomes

Primary

Measure	Time frame
Dass Questionnaire (Stress) 42 BP GSR Reading SPo2Timepoint: 20-22 Days	—

Secondary

Measure	Time frame
NATimepoint: NA	—

Countries

India

Contacts

Public ContactMohit

Dept. of Sangya haran FoA IMS BHU

mohitkumar.dsvv@gmail.com08958066049

Outcome results

None listed

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