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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00670995
Other study ID # 103623B
Secondary ID
Status Completed
Phase Phase 2
First received April 29, 2008
Last updated February 16, 2012
Start date November 2009
Est. completion date November 2010

Study information

Verified date February 2012
Source Deschutes Research, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

There have been a number of tobacco prevention programs developed and tested in the past few years, and some of the comprehensive programs have been promoted by the Office on Smoking and Health at the Centers for Disease Control (CDC). However, the use of these programs and integration into school-based curriculum has been lacking due to a number of factors. We are proposing to develop an interactive computer-based program for tobacco prevention aimed at middle school students. The CD-ROM is designed to be an adjunct to the existing health education curriculum provided for 6th through 8th grade students.


Description:

The CD-ROM is based upon our Phase I prototype program entitled Tobacco World in which students are presented with a video arcade interface that offers them random access to several game-like activities in which they learn about tobacco and the negative health effects associated with tobacco use. We will expand the menu of options to include more complex activities and entertaining games.

The Phase II program will deliver engaging media to educate students about the risks of tobacco and peer and industry influences on their decisions regarding tobacco. Games and activities will be designed to act on mechanisms shown to be effective in decreasing intentions to use tobacco through changing attitudes, social images, beliefs about short and long term physical consequences, perceptions of peers' social images, subjective norms, and perceived behavioral control. We will test individual components of the program with middle school students for effectiveness in changing mediating variables related to initiation and use of tobacco.

The final program will be evaluated in a randomized trial where middle schools in Oregon and New York will be assigned to either an established tobacco prevention curriculum, or to the usual tobacco curriculum plus the Tobacco World program. Students will be assessed at pre-, post- and 6-month follow-up to evaluate the impact of program use on intentions, and actual tobacco use.


Recruitment information / eligibility

Status Completed
Enrollment 1864
Est. completion date November 2010
Est. primary completion date September 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 11 Years to 15 Years
Eligibility Inclusion Criteria:

- Middle school students in 6th or 7th or 8th grade in Oregon and New York City whose parents have consented to have their child participate;

- Middle school health education teachers in Oregon and New York City

Exclusion Criteria:

- Students unable to understand English.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
Interactive Tobacco Education
Increase perceived behavioral control (self-efficacy) Decrease willingness to use tobacco Decrease intentions to use tobacco

Locations

Country Name City State
United States Deschutes Research Inc Eugene Oregon

Sponsors (2)

Lead Sponsor Collaborator
Deschutes Research, Inc. Columbia University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Increase perceived behavioral control (self-efficacy) pre and post No
Secondary Decrease willingness to use tobacco pre and post No
Secondary Decrease intentions to use tobacco pre and post No
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