A Behavioral Application for Improving Smoking Cessation Among Smokers
Part of paid clinical trials in Seattle, Washington.
- Sponsor
- Fred Hutchinson Cancer Center
- Study ID
- NCT07493252
- Status
- Not Yet Recruiting
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Conditions
- Cigarette Smoking-Related Carcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Smartphone app-based Intervention (Actify! A app) — BEHAVIORALUse Actify! A app
- Smartphone app-based Intervention (Actify! B app) — BEHAVIORALUse Actify! B app
- Health Promotion and Education — OTHERReceive motivational messages and smoking cessation information via text messages
- Survey Administration — OTHERAncillary studies
Study Details
This clinical trial compares two smartphone applications, called Actify! (A \& B) for improving smoking cessation outcomes in individuals who smoke. Actify! A is an app grounded in behavioral activation therapy, an evidence-based treatment for depression that can also be used to modify health behaviors such as smoking. The Actify! B app provides evidence-based tobacco cessation strategies based on current clinical guidelines.
Key Dates
- Start date
- Aug 1, 2026
- Status verified
- Mar 2026
- Primary completion
- Jul 31, 2029
- Completion
- Jul 31, 2029
Study Design
- Enrollment
- 1,812 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm I (Actify! A app)Participants use the Actify! app, which helps users identify personal values and meaningful activities, prompts users to schedule and complete meaningful activities, visualizes progress towards meeting activity and smoking-related goals, and provides tailored messages, resources, daily tips, personalized feedback, inspirational messages, and user stories, for 8 weeks on study.
- Active Comparator: Arm II (Actify! B app)Participants use an app, which contains quit advice, tools for tracking smokefree days, progress and cravings, guidance on preparing to quit, managing cravings and withdrawal, recovering from slips, and a mood management feature, for 8 weeks on study.
Primary Outcome Measure
Self-reported 30-day point prevalence abstinence (PPA) from cigarette smoking [ Time Frame: At 6 months post-randomization ]
Central Contacts
- Jaimee Heffner, PhD206-667-7314
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Fred Hutch/University of Washington Cancer Consortium | Seattle | Washington | 98109 | Jaimee Heffner, PhD (PRINCIPAL_INVESTIGATOR) |
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