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| ID | Type | Description | Link |
|---|---|---|---|
| NCI-2018-02552 | Registry Identifier | CTRP (Clinical Trial Reporting Program) | |
| 2009-0351 | Other Identifier | M D Anderson Cancer Center | |
| P30CA016672 | U.S. NIH Grant/Contract | View source | |
| R01CA069425 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Cancer Institute (NCI) | NIH |
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This trial studies how well a new smoking cessation and prevention intervention works in enhancing smoking cessation for university students. The new intervention may be easier to use for students to quit smoke.
PRIMARY OBJECTIVES:
I. To establish the feasibility of a new smoking cessation and prevention intervention including two new modules addressing alcohol use and depression.
II. Demonstrate the feasibility of a smoking prevention website.
OUTLINE: Participants are assigned to 1 of 2 arms.
ARM I: Participants who currently smoke complete a survey over 30 minutes and discuss the survey results with the counselor over 30 minutes at week 2. Participants also complete 3 internet surveys over 20 minutes.
ARM II: Participants who currently do not smoke complete a survey over 30 minutes and discuss the survey results with the counselor over 30 minutes at week 2.
After completion of study, participants are followed up at 3 months.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm I (smoker, survey) | Experimental | Participants who currently smoke complete a survey over 30 minutes and discuss the survey results with the counselor over 30 minutes at week 2. Participants also complete 3 internet surveys over 20 minutes. |
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| Arm II (non-smoker, survey) | Experimental | Participants who currently do not smoke complete a survey over 30 minutes and discuss the survey results with the counselor over 30 minutes at week 2. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Survey Administration | Other | Complete surveys |
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| Measure | Description | Time Frame |
|---|---|---|
| The ease of use and appeal of various features of the program | Up to 5 months | |
| The quality of the interactive multi-media presentations and their ability to generate interest in smoking cessation and prevention | Up to 5 months | |
| Behavior modification determined by EVOLVE Follow up Survey-Smoker | Up to 5 months | |
| Knowledge of modules in the program | Up to 5 months | |
| Feasibility defined as 90% of the student participants indicating that the intervention program is easy to use and can fit into their schedule | Associations between the dependent variables and smoking status will be evaluated with linear and logistic regression models with campus of origin and smoking status as independent predictors of these outcomes. | Up to 5 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Alexander Prokhorov | M.D. Anderson Cancer Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Texas A&M | College Station | Texas | 77843 | United States | ||
| M D Anderson Cancer Center |
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| Label | URL |
|---|---|
| MD Anderson Cancer Center Website | View source |
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| Houston |
| Texas |
| 77030 |
| United States |