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Happy Quit for Smoking Cessation in China

The Efficacy of Mobile Phone-based Text Message Interventions ('Happy Quit') for Smoking Cessation in China

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02693626
Acronym
HQ
Enrollment
1369
Registered
2016-02-29
Start date
2016-08-17
Completion date
2017-11-27
Last updated
2019-02-06

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

Conditions

Smoking Cessation

Keywords

mobile phone-based text message interventions, 'Happy Quit', smoking cessation

Brief summary

The primary objective of this proposed three-year (January 01, 2016 to December 31, 2018) project is to assess whether a program of widely accessed mobile phone-based text message interventions ('Happy Quit') will be effective at helping people in China who smoke, to quit. Based on the efficacy of previous studies in smoking cessation, it is hypothesized that 'Happy Quit' will be an effective, feasible and affordable smoking cessation program in China.

Detailed description

Background: Considering the extreme shortage of smoking cessation services in China, and the acceptability, feasibility and efficacy of mobile phone-based text message interventions for quitting smoking in other countries, here a study of the efficacy of mobile phone-based text message interventions ('Happy Quit') for smoking cessation in Chinahas been proposed. Objectives: The primary objective of this proposed three-year (January 01, 2016 to December 31, 2018) project is to assess whether a program of widely accessed mobile phone-based text message interventions ('Happy Quit') will be effective at helping people in China who smoke, to quit. Based on the efficacy of previous studies in smoking cessation, it is hypothesized that'Happy Quit' will be an effective, feasible and affordable smoking cessation program in China. Methods: In this single-blind, randomized trial, undertaken in China, about 2,000 smokers willing to make a quit attempt will be randomly allocated, using an independent telephone randomization system that includes a minimization algorithm balancing for sex (male, female), age (19-34 or \>34 years), educational level (≤ or \>12 years), and Fagerstrom score for nicotine addiction (≤5, \>5), to 'Happy Quit', comprising motivational messages and behavioral-change support, or to a control group that receives text messages unrelated to quitting. Outcome measures: The primary outcome will be continuous smoking abstinence. A secondary outcome will be point prevalence of abstinence. Abstinence will be assessed by means of brief telephone interviews at six time points (4, 8, 12, 16, 20 and 24 weeks post-intervention). A third outcome will be reductions in number of cigarettes smoked per day. Implications: The results will provide valuable insights into bridging the gap between need and services received for smoking cessation interventions and tobacco use prevention in China. It will also serve as mHealth model for extending the public health significance of other interventions, such as mental health interventions.

Interventions

BEHAVIORALintensive cessation message

Mobile phone-based text message (three to five messages per day) interventions ('Happy Quit') for smoking cessation for 12 weeks with 24 week follow up.

BEHAVIORALNot intensive cessation message

Mobile phone-based text message (three to five messages per week) interventions ('Happy Quit') for smoking cessation for 12 weeks with 24 week follow up.

Sponsors

Purdue University
CollaboratorOTHER
Johns Hopkins Bloomberg School of Public Health
CollaboratorOTHER
Central South University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Daily Chinese cigarette smokers. 2. 18 years of age and older living. 3. Being able to read and write in Chinese. 4. Owning a text-capable cell phone and knowing how to text. 5. Willing to make an attempt to quit smoking in the next month. 6. Willing to provide informed consent to participate in the study.

Exclusion criteria

1. Nonsmokers 2. Below 18 years old. 3. Unable to read and write in Chinese.

Design outcomes

Primary

MeasureTime frame
The primary outcome will be self-reported and biologically verified continuous smoking abstinence.Six month

Secondary

MeasureTime frame
A secondary outcome will be point prevalence of abstinence.six month

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026