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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03169686
Other study ID # 2017S015
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 19, 2020
Est. completion date November 16, 2022

Study information

Verified date November 2022
Source Sir Run Run Shaw Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This proposed project is to assess whether WeChat-based smoking cessation interventions ('WeChat WeQuit' program) will be effective at helping people in China who smoke, to quit.


Recruitment information / eligibility

Status Completed
Enrollment 2000
Est. completion date November 16, 2022
Est. primary completion date November 16, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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 smartphone and knowing how to use WeChat. 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. Smokers without attempt to quit. 3. Below 18 years old. 4. Unable to use smartphone and WeChat. 5. Unable to read and write in Chinese.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive and Behavioral Intervention
Participants who allocate to the intervention group will receive regular smoking cessation related information by professional team.

Locations

Country Name City State
China Yanhui Liao Hanzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Sir Run Run Shaw Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Other Smoking Reduction and Participation Reductions in number of cigarettes smoked per day and rates of participation in and completion of smoking-cessation programs. 26 weeks
Primary Biochemically Validated Continuously Abstinence The primary outcome will be biochemical validation of self-reported 26-week continuous smoking abstinence 26 weeks
Secondary Self-reported 7-day Point Abstinence Self-reported 7-day point-prevalence abstinence at week 1, 4, 8, 12, 16, 20 and 26 after quit date. 26 weeks
Secondary Self-reported Continuous Abstinence Self-reported continuous smoking abstinence rate at weeks 4, 8, 12, 16, 20, and 26 after the quit date. 26 weeks
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