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. Who have tried quitting for atleast one week in past two months and failed and still willing to quit. Those who have responded during the follow up phone calls after enrolling in the camps. Patients from Tobacco cessation center at the hospital who have tried quitting for atleast one week in past two months and failed and still willing to quit. Patients aged 18 and above.
Exclusion criteria
Exclusion criteria: Who use exclusively smoking form of tobacco. Who are not willing to quit the habit. Patients with pre cancerous oral lesions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate quit rates of smokeless-tobacco use after tobacco cessation cunselling and Nicotine replacement therapy intervention.Timepoint: To evaluate quit rates of at the end of 12 weeks after the intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| To estimate the prevalence of tobacco use, willingness to quit and associated oral lesions among those attending oral cancer screening camps/ hospital visit for habit cessation - To estimate the follow up rates for those identified with oral lesions at oral cancer screening campaign/ hospital visit for habit cessation - 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: three months | — |
Countries
India
Contacts
SDM College Of Dental science and Hospital