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Phase 2 Completed N=25 Randomized Treatment

Project Impact 2: A Culturally Tailored Smoking Cessation Intervention for Latino Smokers

Tobacco Use Cessation · Cancer Prevention
Source: ClinicalTrials.gov NCT02596711 ↗
Enrolled (actual)
25
Serious AEs
0.0%
Results posted
Mar 2020
Primary outcomePrimary: Intervention Feasibility & Acceptability — 4.87; 4.71; 4.83 score on a scale

Summary

The goal of this research study is to learn how 3 different kinds of counseling treatments may help individuals to quit smoking.

Outcome Measures

OutcomeResultp-value
PRIMARY
Intervention Feasibility & Acceptability
4.87; 4.71; 4.83
PRIMARY
Patch Adherence: Percentage of Days With Patch
64.6; 68.6; 81.3
PRIMARY
Number of Abstinent Participants
4; 2; 4; 4; 2; 3

Eligibility Criteria

Inclusion Criteria

  • Adults at least 18 years of age
  • Current smoker (>5 cigarettes per day for the past 3 months)
  • Able to speak and read English or Spanish
  • Agree to participate in the study and be available for 6 weeks of treatment and 6 months of follow-up
  • Willing to set a quit date within 2 weeks of enrollment date
  • Identify as being of Latino heritage, ethnicity, or ancestry

Exclusion Criteria

  • Individuals suffering from any unstable medical condition precluding the use of NRT (Identified using the Medical History Questionnaire given at baseline)
  • Currently using smokeless tobacco, electronic nicotine delivery systems (ENDS), nicotine replacement therapy, or other smoking cessation treatment
  • Pregnant or nursing
  • Suffering from a severe psychiatric disorder (assessed using self-reporting history of psychiatric diagnosis during the phone screening) that would interfere with participation
  • Diagnosis of substance dependence other than nicotine (screened using DSM IV TR criteria) Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition
  • Individuals that do not have access to a working telephone
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02596711). 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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