Adults 18 to 30, any sex, with Nicotine Dependence or Nicotine Addiction. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Overall Treatment Satisfaction RatingPrimary· At 3 months post-randomization
We calculated descriptive statistics (mean, standard deviation) for the primary acceptability benchmark of overall satisfaction averaging at least 3.5 on a 1-5 Likert-type scale within the ACT on Vaping arm only.
Overall satisfaction was assessed with a 5-point Likert-type item on the 3-month follow-up survey, with response options ranging from (1) "not at all" to (5) "very much." The ACT on Vaping benchmark average of 3.5 falls between ratings of 3="somewhat" and 4="mostly." Higher values are associated with a higher level of satisfaction.
Group
Value
95% CI
Arm I (Act on Vaping App)
3.8
± 1.3
Change in Readiness to QuitPrimary· From baseline to 3 months post-randomization
Will evaluate differences of Contemplation Ladder scores. The 1-item Contemplation Ladder, scores range from 0-10, was used to assess readiness to quit using e-cigarettes. The higher the score, the more ready the person is to make a change. The anchor for the cut-off score of 5, indicating high vs. low quit readiness, is "Think I should quit but not quite ready."
Group
Value
95% CI
Arm I (Act on Vaping App)
0.96
± 2.0
Arm II (Incentivized Text Message Check-ins)
0.72
± 1.7
Percentage of Participants With a 24-hour Quit AttemptPrimary· At 3 months post-randomization
Making a 24-hour quit attempt between baseline and 3-month follow-up was assessed via self-report at the 3-month follow-up survey. The percentage of participants with self-reported 24-hour quit attempts is evaluated descriptively.
Group
Value
95% CI
Arm I (Act on Vaping App)
21
Arm II (Incentivized Text Message Check-ins)
22
Cotinine-confirmed 30-day Point Prevalence Abstinence From All Nicotine and TobaccoPrimary· At 3 months post-randomization
Complete case, self-reported 30-day abstinence from all nicotine and tobacco products at 3 months, confirmed via saliva cotinine testing. Differences were evaluated descriptively.
Group
Value
95% CI
Arm I (Act on Vaping App)
1
Arm II (Incentivized Text Message Check-ins)
0
Adverse events — posted to ClinicalTrials.gov
Time frame: Adverse events were collected by a web-based survey (on Day 21, 42, 63, and at the 3-month follow-up time point)..
Reporting threshold: 0%.
Adverse-event reports describe events observed during the trial — not all are caused by the drug.
Almost one in ten young adults report current e-cigarette use, putting them at risk of developing nicotine addiction and long-term health effects of exposure to inhaled toxicants. Despite the need for effective treatments to help these young users quit, very few treatments targeting any type of tobacco use among young adults have been evaluated, particularly for young adults who vape and have unique treatment needs. To address these needs, this trial will evaluate a digital program for young adult e-cigarette users at all stages of readiness to quit called ACT on Vaping.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Fred Hutchinson Cancer Center
Last refreshed: 24 June 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05897242.