Community-based Mobile-assisted Brief Intervention for Smoking Cessation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-80
SponsorNational University of Singapore

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

Exposed to any smoking cessation treatment in the past 3 months

Pregnant women

Trial design

Design model

Parallel

Treatments tested in this trial

  • Brief cessation advice + self-help booklet

    Behavioral

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

  • Opt-out referral

    Behavioral

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

  • Mobile chat messaging

    Behavioral

    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.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Mobile-assisted brief interventionExperimental treatment 3 interventions
Group B: Brief adviceActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Biochemically validated smoking abstinence rate

Defined as an exhaled carbon monoxide level of \<5 parts per million or a negative salivary cotinine test (cut off 30ng/mL)

Time frame
6 months
2

Recruitment rate

Number of participants divided by the number of eligible subjects

Time frame
6 months
3

Retention rate

Number of participants completed the follow-up divided by the number of participants

Time frame
6 months

Secondary outcomes

1

Self-reported 7-day point-prevalence smoking abstinence rate

Being completely smoke-free in the past 7 days

Time frame
3 months
2

Self-reported 7-day point-prevalence smoking abstinence rate

Being completely smoke-free in the past 7 days

Time frame
6 months
3

Self-reported smoking reduction rate

Smoking reduction by at least half of the baseline daily number of cigarettes in individuals who continue to smoke

Time frame
3 months
4

Self-reported smoking reduction rate

Smoking reduction by at least half of the baseline daily number of cigarettes in individuals who continue to smoke

Time frame
6 months

Other outcomes

Sponsors and contacts

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