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Community-based Mobile-assisted Brief Intervention for Smoking Cessation

Mobile-assisted Brief Intervention for Smoking Cessation in Community-based Setting: a Pilot Randomised Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07375459
Enrollment
100
Registered
2026-01-29
Start date
2026-02-04
Completion date
2027-03-31
Last updated
2026-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking &Amp; Tobacco Cessation

Keywords

mHealth, WhatsApp, smoking cessation, chat-based intervention, Singapore

Brief summary

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.

Interventions

BEHAVIORALBrief cessation advice + self-help booklet

Participants will receive brief cessation advice following the AWARD (ask, warn, advise, refer, do-it-again) model and a 24-page self-help booklet.

BEHAVIORALOpt-out referral

Research personnel will assist the participant in signing up for the I Quit Programme to receive additional cessation support, unless they decline

Participants will receive personalised chat-based support delivered by a live counsellor for 3 months via WhatsApp. The message will incorporate behaviour change techniques for smoking cessation and mindfulness principles to strengthen participants' capacity to quit smoking.

Sponsors

National University of Singapore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 21 to 80 years * Smoked at least one cigarette daily * Able to communicate and read in English or Chinese * Own a smartphone with WhatsApp installed

Exclusion criteria

* Exposed to any smoking cessation treatment in the past 3 months * Pregnant women

Design outcomes

Primary

MeasureTime frameDescription
Biochemically validated smoking abstinence rate6 monthsDefined as an exhaled carbon monoxide level of \<5 parts per million or a negative salivary cotinine test (cut off 30ng/mL)
Recruitment rate6 monthsNumber of participants divided by the number of eligible subjects
Retention rate6 monthsNumber of participants completed the follow-up divided by the number of participants

Secondary

MeasureTime frameDescription
Self-reported 7-day point-prevalence smoking abstinence rate3 monthsBeing completely smoke-free in the past 7 days
Self-reported smoking reduction rate3 monthsSmoking reduction by at least half of the baseline daily number of cigarettes in individuals who continue to smoke
Self-reported quit attempt rate3 monthsSerious quit attempt that lasted 24 hours or longer
Smoking cessation service use rate3 monthsUse of any smoking cessation service during the follow-up period

Countries

Singapore

Contacts

PRINCIPAL_INVESTIGATORTzu Tsun Luk, PhD, RN

National University of Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 17, 2026