Smoking Cessation Clinical Trial
Official title:
Helping the Poor Quit Smoking: Specialized Quitlines and Meeting Basic Needs
Verified date | December 2023 |
Source | Washington University School of Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Using a 2x2 randomized factorial design, we will conduct a statewide field trial in Missouri to compare the relative and combined effects of these two strategies for augmenting an existing, evidence-based tobacco quitline program. Among 2000 low-income smokers, half will receive standard Missouri quitline services and half will receive new Specialized Quitline services targeted to this group. In each of these groups, half also will receive calls from a trained navigator to help them address unmet Basic Needs and the accompanying psychological distress that act as barriers to smoking cessation.
Status | Completed |
Enrollment | 1944 |
Est. completion date | July 1, 2022 |
Est. primary completion date | July 1, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18 years and older - Missouri resident - English speaking - Not in crisis - Smoke cigarettes every day of the week - Planning to quit smoking in the next 30 days - Comfortable receiving calls from smoking expert and project team - Willing to provide phone numbers to be reached Exclusion Criteria: - Pregnant or planning to become pregnant in the next 3 months - Currently breastfeeding - Insurance through employer - Currently enrolled in smoking quitline |
Country | Name | City | State |
---|---|---|---|
United States | Washington University in St. Louis | Saint Louis | Missouri |
Lead Sponsor | Collaborator |
---|---|
Washington University School of Medicine | National Cancer Institute (NCI), National Institutes of Health (NIH) |
United States,
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* Note: There are 166 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Abstinence 6-months | Report 7-day point prevalence abstinence measured at 6-months post --baseline | 6 months post-baseline | |
Secondary | Abstinence 3-months | Report 7-day point prevalence abstinence measured at 3-months post-baseline | 3 months post-baseline | |
Secondary | 24hr Quit Attempt | Report quitting smoking for at least 24 hours during intervention | 6 months post-baseline |
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