A Study on Visual Vs. Standard Nicotine Replacement Therapy for Smokeless Tobacco Users
Not Applicable
- Conditions
- Health Condition 1: F172- Nicotine dependence
- Registration Number
- CTRI/2024/07/070901
- Lead Sponsor
- Dr Aman Rajput
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Adult patients having age between 18 years to 55 years.
2.Patients willing to give consent for the study.
3.Patients fulfilling the diagnosis of tobacco dependence as per ICD 10 17.24 criteria.
4.Patients having availability of smartphone.
Exclusion Criteria
1.Patients having serious medical conditions requiring priority treatment.
2.Patients having history of using smokeless tobacco since the last 1 year.
3.Women who are pregnant, or intending to become pregnant or lactating mothers.
•Patient having comorbid psychiatric disorder.
•Patients who are unwilling to take NRT or are already on NRT.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Tobacco Cessation Status <br/ ><br> - Measured by Importance Readiness and Confidence (IRC) scale at 2 weeks and 6 weeks <br/ ><br> - Self-reported outcomes: <br/ ><br> - Reduced use <br/ ><br> - Quit attempt (24-hour point period abstinence) <br/ ><br> - Point period abstinence (7-day point period abstinence) <br/ ><br> - Complete abstinence (28-day/4-week point period abstinence) <br/ ><br> - Lapse (slip between abstinence) <br/ ><br> - Relapse <br/ ><br>Timepoint: at Baseline, 2th week, 4th week & 12th week
- Secondary Outcome Measures
Name Time Method rine Cotinine levelTimepoint: After 12 weeks