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N/A Completed N=200 Treatment

Determinants of Smoking Cessation Among Latinos

Source: ClinicalTrials.gov NCT01008748 ↗
Enrolled (actual)
200
Serious AEs
0.0%
Results posted
Mar 2020
Primary outcomePrimary: Number of Participants With 24-Hour Smoking Abstinence (Week 3 Post Quit Day) — 100 Participants

Summary

The goal of this study is to learn how neighborhood and individual factors affect the ability to stop smoking among Spanish-speaking Mexican American (MA) smokers who want to quit smoking.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With 24-Hour Smoking Abstinence (Week 3 Post Quit Day)
100
PRIMARY
24-Hour Smoking Abstinence (Week 26 Post Quit Day)
41
PRIMARY
7-Day Smoking Abstinence (Week 3 Post Quit Day)
76
PRIMARY
7-Day Smoking Abstinence (Week 26 Post Quit Day)
33
PRIMARY
30-Day Smoking Abstinence (Week 26 Post Quit Day)
28
PRIMARY
7-Day Smoking Abstinence (Week 3 Post Quit Day) Intent to Treat
57
PRIMARY
7-Day Smoking Abstinence (Week 26 Post Quit Day) Intent to Treat
20
PRIMARY
7-Day Smoking Abstinence (Week 3 Post Quit Day) Continuous Abstinence
57
PRIMARY
7-Day Smoking Abstinence (Week 26 Post Quit Day) Continuous Abstinence
20

Eligibility Criteria

Inclusion Criteria

  • Current daily smoker who average >/= 5 cigarettes/day for the last year
  • Mexican-American (MA) Adults from the Houston-based MA Cohort Study and/or from the community
  • Age 18 to 65 years
  • Motivated to quit smoking in the next 30 days
  • Viable (working) telephone number and home address
  • Prefers to speak in Spanish
  • Register "8" or more on a carbon monoxide breath test

Exclusion Criteria

  • Contraindication for nicotine patch use
  • Regular use of tobacco products other than cigarettes (cigars, pipes, smokeless tobacco)
  • Use of nicotine replacement therapy products or other smoking cessation medications, other than the nicotine patches supplied during the study
  • Pregnancy or lactation
  • Currently enrolled in a smoking cessation program
  • Participation in a smoking cessation program or study during the past 90 days
  • Another household member is enrolled in this protocol
  • Active substance abuse problem
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01008748). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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