Smoking Cessation Clinical Trial
Official title:
Efficacy and Neuroimaging Mechanisms of Smoking Cessation in China
NCT number | NCT05788068 |
Other study ID # | 20220061 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 1, 2023 |
Est. completion date | August 15, 2023 |
Verified date | August 2023 |
Source | Sir Run Run Shaw Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This proposed project is to assess the efficacy of CBT-based digital smoking cessation interventions in China, as well as explore its neuroimaging mechanisms.
Status | Completed |
Enrollment | 120 |
Est. completion date | August 15, 2023 |
Est. primary completion date | July 15, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 45 Years |
Eligibility | Inclusion Criteria: 1. Use cigarettes for no less than 1 year, and use cigarettes = 10 per day 2. Nicotine dependence (FTCD = 3) 3. Willing to make an attempt to quit smoking in the next month, and have not quit smoking in the past 3 months, and . 4. No other addictions except nicotine 5. Education level of junior high school or above 6. Age between 18 to 45 years old 7. Right-handed 8. No contraindication of MRI scanning 9. Willing to provide informed consent to participate in the study. Exclusion Criteria: 1. Patients who are receiving medication 2. Previous and current mental disorders,and/or mental disorders in line with DSM-5 diagnostic criteria in two departments and three generations. 3. Brain organic disease, brain injury history, coma history 4. Serious physical disease, endocrine disease history, abnormal blood picture, heart, liver and kidney function after examination 5. Pregnant and lactating women |
Country | Name | City | State |
---|---|---|---|
China | Yanhui Liao | Hanzhou | Zhejiang |
Lead Sponsor | Collaborator |
---|---|
Sir Run Run Shaw Hospital |
China,
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. | 4 weeks | |
Primary | Biochemically Validated Continuously Abstinence | Biochemical validation of 4-week continuous smoking abstinence by urine cotinine test. | 4 weeks | |
Primary | Brain Structural Characteristics | Differences of brain structure between successful and unsuccessful smokers after intervention, which will be measured by white matter volume, gray matter volume, cortical thickness, and surface area. | 4 weeks | |
Primary | Brain Functional activity | Differences of whole brain function activity between successful and unsuccessful smokers after intervention, which will be measured by ReHo, ALFF, fALFF, and functional connectivity (FC) | 4 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. | 4 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. | 4 weeks |
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