Tobacco Abuse Cigarette Clinical Trial
Official title:
Helping Hospitalized Patients Quit Smoking
| Verified date | January 2016 |
| Source | Mayo Clinic |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Institutional Review Board |
| Study type | Interventional |
The study is being done to determine whether an in-hospital intervention using a brief
intervention to facilitate quitline utilization will increase quitline utilization by
hospitalized smokers, and will increase post hospital discharge smoking abstinence rates.
Study participants will be randomized to receive either a brief quitline facilitation
intervention , or a control intervention of a brief stop-smoking message.
The study will also compare healthcare costs and utilization in the first six months
following hospitalization between the two groups.
| Status | Completed |
| Enrollment | 600 |
| Est. completion date | November 2015 |
| Est. primary completion date | November 2015 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: Current smoker, Resident of Olmsted County, Inpatient admission to St. Marys or Rochester Methodist Hospital, Able to participate fully in all study aspects, Available for follow-up Exclusion Criteria: Current active treatment for tobacco use initiated prior to hospitalization |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United States | Mayo Clinic in Rochester | Rochester | Minnesota |
| Lead Sponsor | Collaborator |
|---|---|
| Mayo Clinic |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | 7-day point prevalence tobacco abstinence at 6 months after hospitalization | 6 months after hospitalization | No | |
| Secondary | Self-efficacy | Use of Smoking Self-Efficacy Questionnaire 12 | Immediately after the delivery of the brief intervention (day of enrollment) | No |