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Clinical Learning Study for a Mobile Smoking Cessation Program

An Exploratory, Observational, Open-label, Remote Study of Clickotine: A Digital Therapeutic

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04857515
Enrollment
78
Registered
2021-04-23
Start date
2021-03-12
Completion date
2021-06-28
Last updated
2021-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nicotine Dependence, Smoking, Smoking Behaviors, Smoking Cessation, Smoking, Cigarette, Smoking Reduction

Keywords

Smoking Cessation, Smoking Cessation Program, Smoking Cessation Digital Therapeutic

Brief summary

The purpose of this study are to obtain learnings regarding the Digital Therapeutic (DTx) experience of Clickotine, including acceptability and preference of the overall program and specific DTx components, as well as to obtain learnings related to adult participants' use of the DTx for smoking cessation.

Interventions

DEVICEClickotine®

Clickotine is a DTx that contains behavior modification techniques that include controlled breathing, social engagement, personalized messaging, medication access and adherence, digital diversions, and financial incentives.

Sponsors

Click Therapeutics, Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Signed informed consent. * Age 18 and older. * For cigarette smokers: Smokes at least 5 cigarettes a day. For dual-users: Smokes cigarettes AND uses e-cigarettes, with the following additional criteria: * Smokes at least 5 cigarettes a day * Vaping sessions, when they occur, must be for at least 10 minutes (15 puffs) * Fluent in written and spoken English (confirmed by ability to read and comprehend the informed consent form) * Lives in the United States. * Is the solo user of an iPhone with iPhone operating system (iOS)13 or greater capabilities or a smart phone with an Android operating system (OS) 9 or greater capabilities. * Has an active email address. * Willing and able to receive SMS text messages on their smartphone and email messages. * Have access to internet connection during the study duration. * Able to confirm download of installed DTx on baseline date. * Willing and able to comply with study protocol and assessments. * Is willing and able to self-identify sessions of cigarette smoking (1 or more consecutive cigarettes) or vaping (approximately 15 puffs or around 10 minutes in duration) and log those sessions. * Self-reported comfort with and ability to use smartphone apps/programs.

Exclusion criteria

* Prior use of Clickotine. * Currently using a software app for smoking cessation. * Lifetime diagnosis of schizophrenia, psychotic disorder, or pervasive developmental disorders, as per participant self-report. * Any unstable medical illnesses including hepatic, renal, gastroenterological, respiratory, cardiovascular, endocrine, neurologic (including history of severe head injury with loss of consciousness), immunologic, or hematologic disease, as per participant self-report. * Other significant medical condition that, in the opinion of the Investigator or study sponsor, may cofound the interpretation of device efficacy, safety, and tolerability. * Current use of tobacco-containing products other than cigarettes or e-cigarettes (e.g. snuff, chewing tobacco, cigars, or pipes). * Does not have or is unwilling to create a PayPal account

Design outcomes

Primary

MeasureTime frameDescription
The main outcome of the Clickotine Learning Study is to determine acceptability of the digital intervention (DTx).4 MonthsGeneral acceptability of the DTx will be evaluated via surveys for all participants
The main outcome of the Clickotine Learning Study is to determine engagement with the digital intervention (DTx).4 MonthsEngagement with the digital intervention will be measured via app use for all participants
The main outcome of the Clickotine Learning Study is to evaluate attitudes and beliefs regarding the digital intervention.4 MonthsAttitudes and beliefs regarding the digital intervention will be evaluated by interview for selected participants

Secondary

MeasureTime frameDescription
The secondary outcome of the Clickotine Learning Study is to measure engagement levels with the digital intervention for cigarette smokers as compared to dual-users4 MonthsThese engagement levels will be measured via app use.
The secondary outcome of the Clickotine Learning Study is to determine acceptability of the digital intervention for cigarette users as compared to dual-users4 MonthsAcceptability of the digital intervention will be evaluated via survey

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026