About this trial
The purpose of this randomized controlled trial is to assess the efficacy of Actívatexto (Aim 1) and the mediators of the presumed treatment effect (Aim 2) among Latino adults who smoke. Actívatexto is a mobile intervention that integrates four components: 1) a text messaging program that promotes both smoking cessation and physical activity, 2) wearable devices to monitor physical activity, 3) smoking cessation pharmacotherapy \[i.e., nicotine replacement therapies (NRT)\], and 4) an online dashboard where the research team manages participants' incoming and outgoing data from both the text messaging program and wearable devices.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Self-identify as Hispanic and/or Latino
Know how to read and speak English and/or Spanish
Be ≥ 18 years of age
Not meet the recommended levels of physical activity (150 minutes of moderate to vigorous physical activity)
Disqualifiers
Use of tobacco products other than cigarettes in the past 30 days (including e-cigarettes)
Being pregnant or breastfeeding
Plan to move from their current residence in the next six months
Another household member enrolled in the study
Trial design
Parallel
Treatments tested in this trial
Actívatexto
BehavioralActívatexto is a mobile intervention that promotes both smoking cessation and physical activity. Actívatexto integrates four components: 1) a text messaging program that promotes both smoking cessation and physical activity, 2) wearable devices to monitor physical activity, 3) smoking cessation pharmacotherapy (i.e., nicotine replacement therapies), and 4) an online dashboard where the research team manages participants' incoming and outgoing data from both the text messaging program and wearable devices.
Decídetexto
BehavioralDecídetexto is a mobile intervention that solely promotes smoking cessation. Decídetexto integrates three components: 1) a text messaging program that solely promotes smoking cessation, 2) smoking cessation pharmacotherapy (i.e., nicotine replacement therapies), and 3) an online dashboard where the research team manages participants' incoming and outgoing data from the text messaging program.
Treatment groups
Trial outcomes
Primary outcomes
Percent of participants with cotinine verified 7-day point prevalence abstinence
Cotinine levels ≤15 ng/mL in saliva
Secondary outcomes
Percent of participants with self-reported 7-day point prevalence abstinence
No cigarettes, "not even a puff", in the past 7 days
Sponsors and contacts
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University of Rochester
Lead sponsor
National Institute on Minority Health and Health Disparities (NIMHD)
Collaborator
Hackensack Meridian Health
Collaborator