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E-cigarette UseNCT05493982

Evaluation of the Be Vape Free Curriculum of the Tobacco Prevention Toolkit

A study testing Stanford Vaping Prevention curriculum in people with E-cigarette Use, run by Stanford University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 10 to 20 yearsHealthy volunteers can take part
Conditions the study is for
E-cigarette Use
What is being tested?
Stanford Vaping Prevention curriculum
Could I receive a placebo?
No, everyone receives an active treatment
How many people
2,779 participants
Where
1 siteUnited States
Study dates
19 Oct 2022to 8 May 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 10 to 20 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • Middle school and high school students receiving health education at schools participating in the study

Who cannot join

  • None

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Stanford University

    Palo Alto, California, 94304

Other trials in United States

About this study

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. A set of lessons focused on e-cigarette/vaping prevention education specifically is called the Be Vape Free curriculum. The aims of this study are to determine: (1) whether the Be Vape Free curriculum is effective in increasing middle and high school students' resistance to using tobacco and in decreasing positive attitudes towards and intentions to use e-cigarettes; (2) whether the Curriculum is effective in changing middle and high school students' actual use of tobacco; and (3) Examine heterogenous treatment effects identifying groups that benefit the most and those who do not benefit at all from the intervention.

Conditions
E-cigarette Use
Being tested
Stanford Vaping Prevention curriculum
Keywords
youth, tobacco, education, health, prevention, vaping, e-cigarette
Medical subject headings
Vaping

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Stanford Vaping Prevention curriculumBehavioural

    Stanford vaping prevention curriculum delivered as a 5-session course administered in a school classroom setting.

Study groups in NCT05493982
Study groupRoleWhat they receive
Receives Stanford vaping prevention curriculum (pilot phase)ExperimentalStanford vaping prevention curriculum is administered as pilot arm preceding main experimental intervention.
Receives: Behavioral: Stanford Vaping Prevention curriculum
Receives Stanford vaping prevention curriculum (randomized phase)ExperimentalStanford vaping prevention curriculum is administered.
Receives: Behavioral: Stanford Vaping Prevention curriculum
Does not receive Stanford vaping prevention curriculum (randomized phase)No interventionReceives another curriculum or no vaping prevention education.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in e-cigarette use

    Investigator-originated survey measures (questions) assess ever e-cigarette use \& past 30-day tobacco use. This outcome measure assesses e-cigarette use.

    Measured: Change from baseline to follow-up at approximately 156 weeks

  2. Change in intention to use of e-cigarettes scaled score as measured by investigator-originated survey

    This survey measures change in intention to use e-cigarettes with questions related to the participant's knowledge of and resistance to use of e-cigarettes.

    Measured: Change from baseline to follow-up at approximately 156 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Aug 2022
  2. Study start19 Oct 2022
  3. Primary completion8 May 2026
  4. Study completion8 May 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
2,779 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05493982
Sponsor's protocol ID
61965
Other IDs
1R01CA263121
Status last verified
May 2026
First submitted
6 Aug 2022
Last updated
27 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Stanford Vaping Prevention curriculum in people with E-cigarette Use, run by Stanford University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in e-cigarette use (time frame: Change from baseline to follow-up at approximately 156 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 May 2026.

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