To test the effectiveness of the Gain Frame and Loss Frame model for tobacco cessatio
Not Applicable
Completed
- Conditions
- Health Condition 1: K135- Oral submucous fibrosis
- Registration Number
- CTRI/2023/07/055468
- Lead Sponsor
- Dr. D.Y.Patil Dentl College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 104
Inclusion Criteria
1.Subjects that are willing to participate in the study.
2.Participants for Group IA and Group IIA individuals who are exclusively smoking tobacco users and for Group IB and Group IIB individuals who are exclusive smokeless tobacco users.
3.The participant is a current tobacco user.
4.Participants who are literate and able to read and write.
Exclusion Criteria
1.Subjects who are users of both the forms of tobacco.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tobacco cessation using Gain Frame and Loss frame modelTimepoint: Data will be recorded at baseline and after 6 months.
- Secondary Outcome Measures
Name Time Method To evaluate which group showed increased improvement after the tobacco cessation intervention.Timepoint: Data will be collected at baseline and then after 6 months.