Intervention study to find the Nicotine dependence among Smokeless Tobacco users
Phase 3
- Registration Number
- CTRI/2024/01/061447
- Lead Sponsor
- Mrs.Chaithra Nayak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
It includes
1.Participants who use smokeless Tobacco
2. Participants who are in the age group from 18 to 40 years
3. Participants who are willing to take part in the study
4. Participants who knows to read and write Kannada
5. Participants who are available at the time of Intervention
Exclusion Criteria
It includes
1. Participants who have medical illness
2. Participants who have any psychiatric disorders
3.Participants who are taking treatment for any other disorders
4.Participants who are available at the time of Intervention
5.Participants who those who have not come for Intervention after three weeks
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcomes <br/ ><br>To evaluate the effectiveness of Behavioural Intervention to reduce the level of Nicotine dependence among Smokeless Tobacco users <br/ ><br>Timepoint: The experimental group will be subjected to Behavioural Intervention for a period of 3 weeks as one session per week. Baseline outcome measures & nicotine dependence using FTND before Intervention for all the participants. <br/ ><br>Post-test will be taken up after the 3rd Week by follow up & assessing Nicotine dependence. The effectiveness will be assessed at 3rd & 6th Month through FTND <br/ ><br>
- Secondary Outcome Measures
Name Time Method To evaluate the Nicotine dependance among Smokeless tobacco users <br/ ><br>To find the association between the smokeless tobacco users with a selected sociodemographic profile <br/ ><br>aware about the ill effects of SLT Consumption & attempt to quit.Timepoint: 3 weeks