Tobacco Dependence Treatment Education for Dental Students

This study is enrolling participants by invitation only.
Sponsor:
Information provided by (Responsible Party):
University of Louisville
ClinicalTrials.gov Identifier:
NCT01522924
First received: January 24, 2012
Last updated: February 24, 2012
Last verified: January 2012

January 24, 2012
February 24, 2012
February 2012
April 2012   (final data collection date for primary outcome measure)
Cessation treatment abilities [ Time Frame: 3 months ] [ Designated as safety issue: No ]
Outcome measurements include changes in dental students' attitudes, perceived barrier,subjective norms, perceived skills, self-efficacy, intentions to provide cessation treatment, and tobacco cessation knowledge after completing a cessation treatment educational activity using standardized patients.
Same as current
Complete list of historical versions of study NCT01522924 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Tobacco Dependence Treatment Education for Dental Students
Tobacco Dependence Treatment Education for Dental Students Using Standardized Patients

There is a difference in dental students' attitudes, perceived barriers, subjective norms, perceived skills, self-efficacy, intentions to provide cessation treatment, and cessation knowledge in those students receiving a tobacco cessation lecture along with practice sessions using standardized patients and those students receiving only a tobacco cessation lecture. Dental students' use of tobacco does affect their intent to provide cessation treatment to patients. The time between receiving the lecture and participating in the practice sessions using standardized patients makes a difference in dental students' attitudes, perceived barriers, subjective norms. perceived skills, self-efficacy, intentions to provide cessation treatment, and cessation knowledge.

The experimental study has a pretest-posttest design. It evaluates the changes to dental students' attitudes, perceived barriers, subjective norms, perceived skills, self-efficacy, intentions to provide cessation treatment, and tobacco cessation knowledge between those students receiving a lecture along with practice sessions using standardized patients and those students receiving only a lecture. Dental students will be invited to complete two questionnaires. The control group of dental students will complete the first questionnaire before the lecture and the second questionnaire after the lecture. The experimental group of dental students will complete the first questionnaire before the lecture and the second questionnaire after the lecture and the practice and debriefing sessions. Subjects will include 120 first year dental students in an introductory course to clinical dentistry. The cessation training is a required activity in the course. Students are divided into small groups according to their bench or lab numbers. These numbers are assigned to the student based on the alphabetical order of their name. The eligibility criteria is: 1) Must be a first year dental student in Introduction to Clinical Dentistry 1 at the University of Louisville, and 2) Must be willing to volunteer to complete pre- and post-questionnaires about the cessation treatment educational program. The exclusion criteria is: Subject is not willing to give consent to complete the pre- and post- questionnaire.

Interventional
Phase 2
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Smoking
  • Other: Lecture only
    Tobacco cessation treatment educational intervention using lecture only
    Other Names:
    • Tobacco dependence
    • Cessation treatment
    • Tobacco cessation treatment education
    • Standardized patients
    • Cessation counseling
    • Dental students
  • Other: Counseling practice sessions
    Dental students will complete the first questionnaire before a tobacco cessation lecture and the second questionnaire after the lecture, counseling practice sessions using standardized patients and a debriefing session.
    Other Names:
    • Tobacco cessation treatment education
    • Tobacco cessation counseling
    • Smoking cessation counseling
    • Tobacco dependence treatment
    • Standardized patients
  • Experimental: Counseling practice sessions
    Dental students will be administered the first questionnaire before receiving a tobacco cessation lecture and the second questionnaire after the lecture, counseling practice sessions using standardized patients, and debriefing session.
    Intervention: Other: Counseling practice sessions
  • No Intervention: Lecture only
    Dental students will be administered the first questionnaire before the tobacco cessation lecture and the second questionnaire after the lecture and before the counseling practice sessions using standardized patients and debriefing session.
    Intervention: Other: Lecture only
Walsh SE, Singleton JA, Worth CT, Krugler J, Moore R, Wesley GC, Mitchell CK. Tobacco cessation counseling training with standardized patients. J Dent Educ. 2007 Sep;71(9):1171-8.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Enrolling by invitation
120
April 2012
April 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • must be a first year dental student in Introduction to Clinical Dentistry I at the University of Louisville and
  • volunteer to complete pre- and post-questionnaires concerning tobacco cessation treatment educational training.

Exclusion Criteria:

  • subject does not complete pre- and post- questionnaires.
Both
18 Years to 65 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01522924
12.0026
No
University of Louisville
University of Louisville
Not Provided
Principal Investigator: Jacqueline A Singleton, MEd University of Louisville
University of Louisville
January 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP