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Effectiveness Of Yogic Interventions

A Randomized Controlled Trial Of The Feasibility And Initial Effectiveness Of Yogic Interventions In Tertiary Cancer Care For Tobacco Cessation: Pilot Study - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074352
Enrollment
110
Registered
2024-09-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

None listed

Interventions

Intervention1: Yogic Intervention: Experimental group- Participants Involving Technique 10 Deep Breaths When Craving Tobacco Only Experimental group- 20 min of 3HZ frequency music using app (morni

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Current Tobacco Users (smoker or Smokeless Tobacco) Willingness to participate in the study

Exclusion criteria

Exclusion criteria: Severe medical conditions contraindicating yoga practice Cognitive impairment or inability to provide informed consent

Design outcomes

Primary

MeasureTime frame
The study will assess the practicality and acceptability of implementing yogic interventions in a tertiary cancer care setting, including factors such as patient and healthcare provider engagement, program adherence, and any challenges encountered during the trial. Timepoint: 6 MONTH

Secondary

MeasureTime frame
Initial Effectiveness: The study will evaluate the immediate impact of yogic interventions on tobacco cessation outcomes, such as: Quit rates: The proportion of participants who successfully quit smoking or using tobacco products during the trial period. Cigarette consumption: The average number of cigarettes smoked per day or other tobacco products consumed reduces after the intervention. Craving: The frequency and intensity of tobacco cravings experienced by participants can reduced after the intervention. Stress and anxiety: The levels of stress and anxiety reported by participants can be reduced after the intervention.Timepoint: 6 MONTH

Countries

India

Contacts

Public ContactJyotiben Somabhai Patel

Tata Memorial Hospital

jyotitmh21@gmail.com9167092270

Outcome results

None listed

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