Trial · NCT07895784
Effectiveness Of Project EX: A Classroom-Based Smoking Prevention And Cessation Intervention Program
NCT07895784, Not applicable, Not yet recruiting, University of Karachi
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effectiveness Of Project EX: A Classroom-Based Smoking Prevention And Cessation Intervention Program. Trials, record NCT07895784. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07895784
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effectiveness Of Project EX: A Classroom-Based Smoking Prevention And Cessation Intervention Program
- NCT number
- NCT07895784
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 600 participants, estimated
- Lead sponsor
- University of Karachi
- Conditions
- Focus of the Study is Smoking Cessation and Prevention, Smoking Prevention
- Interventions
- Project EX
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change from Baseline in Mean motivation to quit tobacco use Score . | Baseline, 6 weeks (post-intervention), and 6 months (follow-up) | Measured with self-report items on the likelihood of motivation to quit in the future. Lower scores indicate greater motivation to quit. |
| Primary | Change from Baseline in Mean Smoking Intention Score. | Baseline, 6 weeks (post-intervention), and 6 months (follow-up) | Measured with self-report items on the likelihood of smoking in the future. Lower scores indicate greater intention to smoke. |
| Primary | Change from Baseline in Mean Tobacco norm attitude Score | Baseline, 6 weeks (post-intervention), and 6 months (follow-up) | Scale assessing perceived acceptability of tobacco use among peers. Lower scores indicate more favorable attitudes toward tobacco use. |
| Primary | Change from Baseline in Mean Self control Score | Baseline, 6 weeks (post-intervention), and 6 months (follow-up) | Scale assessing self control items. Higher scores indicate greater self-control. |
| Primary | Change from Baseline in Mean depression Score | Baseline, 6 weeks (post-intervention), and 6 months (follow-up) | Measured with the Center for Epidemiologic Studies Depression Scale (CES-D). Higher scores indicate more depressive symptoms. |
| Primary | Change from Baseline in Smoking-Related Knowledge | Baseline, 6 weeks (post-intervention), and 6 months (follow-up) | Measured the health consequences of smoking. Higher scores indicate greater knowledge. |
| Primary | Change from Baseline in Endorsement of Tobacco Use Myths | Baseline, 6 weeks (post-intervention), and 6 months (follow-up) | Measured on common misconceptions about tobacco use. |
| Primary | Change from Baseline in Tobacco Use Behavior | Baseline, 6 weeks (post-intervention), and 6 months (follow-up) | Measured with self-report items on frequency and amount of tobacco use (cigarettes and other tobacco products) in the past 30 days. Higher scores indicate greater tobacco use. |
| Primary | Change from Baseline in Quit Attempts | Baseline, 6 weeks (post-intervention), and 6 months (follow-up) | Measured with self-report items on whether, and how many times, students who use tobacco tried to quit since the previous assessment. |
| Primary | Change from Baseline in Coping | Baseline, 6 weeks (post-intervention), and 6 months (follow-up) | Measured with items assessing ways of coping with stress and difficult situations without tobacco use. This scale's items are divided into good coping and bad coping |
1 to 10 of 12Source ClinicalTrials.gov
See all 12 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07895784
GET https://conductscience.org/api/trials/v1/NCT07895784/registered