Evaluation of The Stanford Tobacco Prevention Toolkit

Not Applicable

Withdrawn

• Conditions: Behavior, Smoking; Behavior, Health
• Interventions: Behavioral: Stanford Tobacco Prevention Toolkit curriculum

• Registration Number: NCT04467034
• Lead Sponsor: Stanford University

Brief Summary

The Stanford Tobacco Prevention Toolkit is a free online curriculum developed for use by educators and health professionals in providing tobacco-specific prevention education to middle and high school students. The aims of this study are to determine: (1) whether the Curriculum is effective in changing middle and high school students' resistance to using tobacco as well as knowledge of, attitudes towards, and intentions to use different tobacco products; and (2) whether the Curriculum is effective in changing middle and high school students' actual use of tobacco in the short-term.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2020-05-21
• Study First Submitted QC: 2020-07-07
• Study First Posted: 2020-07-10
• Study Start: 2021-10-15
• Primary Completion: 2022-04-30
• Study Completion: 2022-05-31
• Status Verified: 2022-08
• Last Update Submitted: 2022-08-19
• Last Update Posted: 2022-08-23

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Middle school and high school students

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Exclusion Criteria

• Non English-speakers

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Receives Stanford tobacco education curriculum	Stanford Tobacco Prevention Toolkit curriculum	Stanford Tobacco Prevention Toolkit is administered.

Primary Outcome Measures

Name	Time	Method
Change in resistance to use of tobacco products scaled score as measured by investigator-originated survey	Change from baseline to follow-up at approximately 40 weeks post-baseline	This survey measures change in resistance to use of tobacco products with questions related to the participant's intention to use tobacco.

Secondary Outcome Measures

Name	Time	Method
This survey measures use of tobacco products with questions related to the participant's ever tobacco use, past 30-day tobacco use, and past 7-day tobacco use.	Change from baseline to follow-up at approximately 40 weeks post-baseline	Investigator-originated survey survey measures (questions) assess ever tobacco use, past 30-day tobacco use, past 7-day tobacco use This outcome measure assesses tobacco products use.
Change in skills for refusal of tobacco products scaled score as measured by investigator-originated survey	Change from baseline to follow-up at approximately 40 weeks post-baseline	This survey measures change in skills to refuse tobacco use with questions related to the participant's susceptibility to tobacco use, self-efficacy and self-confidence.
Change in knowledge of tobacco products scaled score as measured by investigator-originated survey	Change from baseline to follow-up at approximately 40 weeks post-baseline	This survey measures knowledge of tobacco products with questions related to the participant's knowledge of ingredients, of nicotine levels, of potential health outcomes.

Trial Locations

Locations (1)

Stanford University; 🇺🇸 Palo Alto, California, United States