Health Condition 1: K088- Other specified disorders of teethand supporting structures
Conditions
Interventions
Intervention1: BEHAVIOURAL COUNSELLING: Participants will be given a brief advice on harmful effect of tobacco and enrolled in the National Tobacco Quitline Services (NTQLS) through the designated tol
Sponsors
Dr SATYAPRABHA ROUT
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients of all age groups referred to TCC of SCB Dental College and Hospital, Cuttack will be included in the study. 2.Individuals who are current users of smokeless tobacco products (such as gutkha, khaini, pan masala with tobacco, snuff, or other forms). 3.Individuals who are willing to quit smokeless tobacco. 4.Individuals willing to participate in the cessation intervention.
Exclusion criteria
Exclusion criteria: 1.Individuals who consume or use smoked tobacco products only (cigarettes/bidis) without smokeless tobacco use. 2.Individuals who are currently enrolled in any other tobacco cessation program or clinical trial. 3.Individuals receiving pharmacotherapy for tobacco cessation (nicotine replacement therapy, bupropion, varenicline, or other medications) at the time of recruitment. 4.Individuals with serious medical illnesses or unstable systemic conditions that may interfere with participation or follow-up (e.g., severe cardiac disease, uncontrolled diabetes, or malignancy). 5.Individuals with psychiatric disorders or cognitive impairment that limit their ability to provide reliable information or informed consent. 6.Individuals who are not willing to provide informed consent or unable to comply with the study protocol and scheduled follow-up visits. 7.Participants who plan to relocate or are unlikely to be available for the 24-week follow-up period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Point prevalence abstinence from smokeless tobacco use at 4,8,12,24 weeksTimepoint: 4,8,12,24 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Prolonged abstinence (continuous cessation) over a period of 24 weeks 2.Number and frequency of quit attempts 3.Proportion of participants with relapse 4.Salivary cotinine level assessment at the end of 24 weeks. Timepoint: 6 MONTHS | — |
Countries
India
Contacts
Public ContactDr HEMAMALINI RATH
SCB DENTAL COLLEGE AND HOSPITAL,CUTTACK,ODISHA, Odisha
Outcome results
None listed