None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adults (age group :18 60 years) 2. Current users of smoked tobacco. 3. Participants in the precontemplation stage. 4. Participants who have consumed tobacco [smoking] within a past period of 6 months. 5. Participants who are willing to participate in the study and provided written informed consent. 6. Participants possessing a smartphone (Android or iOS), having regular access to e-mail services, and willing to provide valid contact details including postal address, telephone number, and e-mail address for follow-up purposes. 7. Available for further follow up visits or should be able to attend counselling sessions to be a part of intervention.
Exclusion criteria
Exclusion criteria: 1.Individuals with systemic or psychiatric illness affecting participation. 2.Patients currently undergoing any other tobacco cessation therapy or using any pharmacotheraphy for cessation. 3.Pregnant or lactating women. 4.Participants with acute or chronic illnesses, sensory impairments (such as blindness or deafness), or intellectual disabilities that could interfere with comprehension of instructions or participation in the study procedures were excluded. 5.Participants unwilling to comply with follow-up visits.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tobacco cessation with reduced CO levels and nicotine dependence Improved motivation and readiness to quit Better oral health (periodontal status & mucosal lesions) Combined intervention most effectiveTimepoint: baseline,1 week, 2 weeks ,4 weeks, 8 weeks, 3 months, 6 months, and 12 months | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Kalinga Institute of Dental Sciences (KIDS)