ClinicalTrials.gg
RecruitingNCT06926608Updated Sep 18, 2026

Actívatexto: Advancing Smoking Cessation and Physical Activity Among Latinos

An interventional study of Actívatexto and Decídetexto in Smoking, Smoking Cessation and Physical Inactivity, sponsored by University of Rochester. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-18.

Sponsored by University of Rochester · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Jun 2025; still recruiting 1 year 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
408
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

We will conduct a two-arm randomized controlled trial among Latinos who smoke and do not meet the recommended levels of physical activity (N=408). Participants will be recruited via community-based efforts and randomly assigned in a 1:1 ratio to Actívatexto (a mobile intervention that promotes both smoking cessation and physical activity) or Decídetexto (a mobile intervention that solely promotes smoking cessation). All participants will be provided with nicotine replacement therapies and a Fitbit Versa 4 device. Participants in both groups will complete a baseline assessment at enrollment and follow-up assessments at Months 3 and 6.

02

Conditions studied

  • Smoking
  • Smoking Cessation
  • Physical Inactivity
03

In context

Smoking

1,509 studies on the registry are indexed under Smoking; 193 are open to participants now.

This study's planned enrollment of 408 is above the median of 115 across 1,164 interventional studies indexed under Smoking.

Browse Smoking studies →

Lead sponsor

University of Rochester is the lead sponsor of 729 studies on the registry; 116 are open to participants now.

Of its 56 completed or terminated interventional studies of FDA-regulated products, 44 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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)
  • Smoke cigarettes at least 3 days per week
  • Be interested in quitting smoking in the next 30 days
  • Have a cellphone with text messaging capability
  • Know how to utilize text messages
  • Be willing to wear a wearable device daily to monitor physical activity
  • Be willing to complete all study visits

Exclusion criteria

Exclusion Criteria:

  • 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
  • Unable to become more physically active or engage in a fitness appraisal
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
408 participants (estimated)

Study arms

  • Experimental
    Actívatexto

    Actívatexto 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.

    Behavioral: Actívatexto

  • Active comparator
    Decídetexto

    Decídetexto 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.

    Behavioral: Decídetexto

Interventions

  • BehavioralActívatexto

    Actívatexto 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.

  • BehavioralDecídetexto

    Decídetexto 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.

06

What researchers measure

Primary outcomes

  1. Percent of participants with cotinine verified 7-day point prevalence abstinence

    Cotinine levels ≤15 ng/mL in saliva

    Time frame: Month 6

Secondary outcomes

  1. Percent of participants with self-reported 7-day point prevalence abstinence

    No cigarettes, "not even a puff", in the past 7 days

    Time frame: Month 6

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06926608
Responsible party
Francisco Cartujano, MD (Assistant Professor, University of Rochester) — Principal investigator
First posted
Apr 13, 2025
Start date
Jun 17, 2025
Primary completion
May 31, 2029 (estimated)
Completion
May 31, 2029 (estimated)
Last update
Sep 18, 2026

Study contacts

Francisco Cartujano, MD
Contact
francisco_cartujano@urmc.rochester.edu
(585) 273-1646

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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