effect of non pharmacological (5A)intervention in smokeless tobacco userS
- Conditions
- Health Condition 1: F172- Nicotine dependence
- Registration Number
- CTRI/2023/11/060208
- Lead Sponsor
- AIIMS New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Age 18 to 60 years.
Male
Current (last 1 month) users of Smokeless tobacco and those who report daily use of smokeless
tobacco in the past 1 year.
Diagnosed with nicotine dependence as per ICD-11 criteria.
Currently receiving dental treatment in CDER. Patients who have to follow up for dental treatment at CDER (center for dental education and research).
Willing to participate in telephonic follow up at 4 weeks and in-person follow up at 12 weeks.
History of co-morbid psychiatric illnesses (as assessed by WHO self-report questionnaire)
Patient unable to chew tobacco and or smoke due to oral lesions
Smoked tobacco in the past 1 year
WHO- ASSIST scores more than or equal to 10 for alcohol or more or equal to 4 for other substances except tobacco.
Has ever received tobacco cessation intervention (except simple advice from a health care professional) in the past
Presence of any terminal condition for e.g. malignancy
Unwilling to give informed consent for the study
Unable to understand and communicate with the interviewer
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 7 day point prevalence of abstinence Ascertained by screening for the salivary cotinine. Reduction in smokeless tobacco use as measured by the number of chews per day <br/ ><br> <br/ ><br>Timepoint: 4 weeks and 12 weeks
- Secondary Outcome Measures
Name Time Method Change in the stage of motivation <br/ ><br>Number of quit attempts <br/ ><br> <br/ ><br>lasting more than 24 hours <br/ ><br>Timepoint: 4 weeks,12 weeks