None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients attending oral cancer screening campaign Those who use smokeless form of tobacco or mixed. Those willing to undergo oral examination and willing to participate in a two-month community-based behavioral intervention program on smokeless tobacco cessation. Patients aged 18 and above.
Exclusion criteria
Exclusion criteria: Volunteers who are not available during follow up. Participants with severe withdrawal symptoms
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate quit rates of smokeless-tobacco use after Community based behavioral intervention (Group A) at two months following oral cancer screening campaign. • To evaluate quit rates of smokeless-tobacco use after One time health advice (Group B) at two months following oral cancer screening campaign. • To compare quit rates of smokeless-tobacco use after Community based behavioral intervention (Group A) with One time health advice (Group B) at two months following oral cancer screening campaign.Timepoint: Two months | — |
Secondary
| Measure | Time frame |
|---|---|
| To estimate the prevalence of tobacco use, willingness to quit and associated oral lesions among those attending oral cancer screening campaign. ? To estimate the follow up rates for those identified with oral lesions at oral cancer screening campaign. ? To estimate the cost effectiveness of the program in terms of quit rates achieved. ? To evaluate the influence of demographic factors, type of tobacco used and degree of tobacco dependence on the quit rates.Timepoint: Two months | — |
Countries
India
Contacts
SDM College of Dental Sciences and Hospital, Shri Dharmasthala Manjunatheshwara University, Dharwad