Xylitol Gum for Promoting Smoking Cessation
NCT07240545 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 134
Last updated 2025-11-21
Summary
The goal of this clinical trial is to learn if 4-week xylitol gum intervention works to promote smoking cessation in daily smokers. It will also learn about the feasibility and acceptability of using xylitol gum. The main questions it aims to answer are:
(1)Does xylitol gum help to reduce cigarette consumption and promote smoking cessation?
Researchers will compare 4-week xylitol gum intervention to the brief advice to see if xylitol gum works to promote smoking cessation.
Participants in the intervention group will receive a 3-month behavioral intervention comprising a 4-week xylitol gum aligned with 12 weeks of instant reminder message support.
Conditions
- Smoking Cessation
- Health Promotion
Interventions
- BEHAVIORAL
-
Self-help smoking cessation booklet
The self-help smoking cessation booklet includes commonly used smoking cessation strategies.
- BEHAVIORAL
-
Brief smoking cessation advice
Brief smoking cessation advice guided by the validated AWARD model (Assess, Warning, Advice, Refer, and Do-it-again).
- BEHAVIORAL
-
Warning leaflet
The warning leaflet contains pictorial depictions of the adverse health effects of smoking.
- BEHAVIORAL
-
4-week xylitol gum intervention
Participants in the intervention group will receive 4 packs of xylitol gum (approximately US $2 per pack) at baseline and will be encouraged to use it when they experience cravings.
- BEHAVIORAL
-
Instructional leaflet
The instructional leaflet includes the potential benefits of xylitol gum for smoking cessation, recommended timing and dosage for use, and appropriate disposal of used gum.
- BEHAVIORAL
-
12-week instant message support
Approximately 24 reminder messages (two per week), developed based on the Love and Care Approach framework, will be delivered over the 12-week period to reinforce motivation and adherence.
Sponsors & Collaborators
-
The University of Hong Kong
lead OTHER
Principal Investigators
-
Man Ping Wang, PhD · The University of Hong Kong
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-11-24
- Primary Completion
- 2026-02-28
- Completion
- 2026-09-30
Countries
- Hong Kong
Study Locations
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