Smoking Cessation Clinical Trial
Official title:
Dissemination of an Inpatient Smoking Cessation Program to South Carolina Hospitals Study #1
Verified date | January 2024 |
Source | Medical University of South Carolina |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The modest goal of this study is to replicate the behavioral outcomes of the opt out MUSC-Tobacco Treatment Program in the following three patient groups: 1) psychiatric inpatients housed in the Institute of Psychiatry (IOP) in Charleston; 2) non-IOP patients seen in Charleston; and 3) patients seen in the other four MUSC affiliated hospitals combined (i.e., Chester, Florence, Lancaster, and Marion). The aims and the design/methods utilized for evaluation will be the same for each of the three patient groups.
Status | Active, not recruiting |
Enrollment | 1122 |
Est. completion date | January 2025 |
Est. primary completion date | January 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18+ years and older - hospitalized cigarette smokers eligible for either enhanced or basic care - discharged from the hospital back to their home Exclusion Criteria: - patients without a phone number - those unable to communicate in the English language |
Country | Name | City | State |
---|---|---|---|
United States | Institute of Psychiatry | Charleston | South Carolina |
United States | MUSC | Charleston | South Carolina |
United States | MUSC | Chester | South Carolina |
United States | MUSC | Florence | South Carolina |
United States | MUSC | Lancaster | South Carolina |
United States | MUSC | Marion | South Carolina |
Lead Sponsor | Collaborator |
---|---|
Medical University of South Carolina |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Self-reported smoking prevalence 6-weeks after hospitalization. | Hypothesize that patients exposed to the enhanced care intervention compared to basic care will report a 2-fold higher 7-day non-smoker prevalence rate after hospitalization (i.e., 20% vs 10%) | Assessed 6-weeks post-discharge | |
Primary | Self-reported use of FDA Approved Smoking Cessation Medication | Hypothesize that patients exposed to the enhanced care intervention compared to basic care will report a 2.5-fold greater use of an FDA approved stop smoking medication after hospitalization (i.e., 20% vs 8%) | Assessed 6-weeks post-discharge |
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