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OpenTrials
Completed

NCT Number: NCT00941395

Enhanced Smoking Cessation for University Students

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.

Completed

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Key information

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Texas A&M, College Station, Texas, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • CESSATION ARM: Student at University of Houston Central Campus or Texas A&M University
  • CESSATION ARM: Smoke 1 or more cigarettes a day
  • CESSATION ARM: Speak and read English
  • CESSATION ARM: Signed informed consent and an acknowledgement of participation requirements
  • CESSATION ARM: Be enrolled in at least one class at respective campus at baseline
  • CESSATION ARM: Provide current contact information
  • CESSATION ARM: Have access to the Internet
  • PREVENTION ARM: Student at University of Houston Central Campus or Texas A&M University
  • PREVENTION ARM: Speak and read English
  • PREVENTION ARM: Signed Informed Consent and an acknowledgement of participation requirements
  • PREVENTION ARM: Be enrolled in at least one class at respective campus at baseline
  • PREVENTION ARM: Provide current contact information
  • PREVENTION ARM: Have access to the Internet
  • PREVENTION ARM: Evidence of smoking susceptibility (as defined by the Smoking Susceptibility Scale)
  • CESSATION ARM: Willing to answer all survey questions on all survey instruments throughout the duration of study
  • PREVENTION ARM: Willing to answer all survey questions on all survey instruments throughout the duration of study

Exclusion criteria

  • CESSATION ARM: Evidence of major depressive disorder (as defined by PHQ-9 [Patient Health Questionnaire-9])
  • CESSATION ARM: Evidence of severe alcohol abuse (as defined by AUDIT [Alcohol Use Disorders Identification Test] measure)
  • PREVENTION ARM: Current tobacco use
  • PREVENTION ARM: Does not plan to continue as a student at their campus for at least one more year
  • CESSATION ARM: Does not plan to continue as a student at their campus for at least one more year
  • PREVENTION ARM: Evidence of major depressive disorder (as defined by PHQ-9 [Patient Health Questionnaire-9])
  • PREVENTION ARM: Evidence of severe alcohol abuse (as defined by AUDIT measure)
  • CESSATION ARM: Pregnancy

Treatment and study plan

Survey Administration

Other

Complete surveys

Primary outcomes

  1. The ease of use and appeal of various features of the program

    Time frame: Up to 5 months

  2. The quality of the interactive multi-media presentations and their ability to generate interest in smoking cessation and prevention

    Time frame: Up to 5 months

  3. Behavior modification determined by EVOLVE Follow up Survey-Smoker

    Time frame: Up to 5 months

  4. Knowledge of modules in the program

    Time frame: Up to 5 months

  5. Feasibility defined as 90% of the student participants indicating that the intervention program is easy to use and can fit into their schedule

    Time frame: Up to 5 months

    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.

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Important dates

Study start
2009
Primary completion
2017
Study completion
2017
First posted
Jul 17, 2009
Registry last updated
Nov 21, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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