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Community-based Mobile-assisted Brief Intervention for Smoking Cessation

N

National University of Singapore

Status

Not yet enrolling

Conditions

Smoking &Amp; Tobacco Cessation

Treatments

Behavioral: Opt-out referral
Behavioral: Mobile chat messaging
Behavioral: Brief cessation advice + self-help booklet

Study type

Interventional

Funder types

Other

Identifiers

NCT07375459
NUS-IRB-2025-690

Details and patient eligibility

About

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.

Enrollment

100 estimated patients

Sex

All

Ages

21 to 80 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

Mobile-assisted brief intervention
Experimental group
Treatment:
Behavioral: Brief cessation advice + self-help booklet
Behavioral: Mobile chat messaging
Behavioral: Opt-out referral
Brief advice
Active Comparator group
Treatment:
Behavioral: Brief cessation advice + self-help booklet

Trial contacts and locations

1

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Central trial contact

Tzu Tsun Luk, PhD, RN; Joey TW Tyoh, BSc, RN

Data sourced from clinicaltrials.gov

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