The goal of this pilot trial is to evaluate the feasibility of a mobile-assisted brief intervention for smoking cessation in community-based individuals in Singapore. Specific aims include: 1. To assess how many eligible individuals accept the invitation to participate in the trial 2. To assess the retention of the participants through 6 months after treatment initiation 3. To assess the acceptability of the intervention in terms of participants' engagement and ratings 4. To examine the intervention effect on abstinence outcomes Participants will be randomly assigned to either the intervention group or control group and followed for 6 months from randomisation.
Age range
21 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Biochemically validated smoking abstinence rate
Timeframe: 6 months
Recruitment rate
Timeframe: 6 months
Retention rate
Timeframe: 6 months