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Clinical Trials/NCT01811758
NCT01811758
Completed
Phase 1

Culturally Specific Interventions and Acculturation in African American Smokers

University of Miami1 site in 1 country345 target enrollmentAugust 2011

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Smoking
Sponsor
University of Miami
Enrollment
345
Locations
1
Primary Endpoint
7-day point prevalence abstinence
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The investigators expect that a culturally specific group intervention targeting African American smokers will result in greater smoking cessation rates compared to a standard intervention.

Registry
clinicaltrials.gov
Start Date
August 2011
End Date
April 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Monica W. Hooper

Associate Professor

University of Miami

Eligibility Criteria

Inclusion Criteria

  • self-identification as African American
  • current smoker of ≥ 5 cigarettes/day or expired CO level of ≥ 8 ppm;
  • able to speak and read English;
  • permanent contact information;
  • access to transportation by public transit or car;
  • no current behavioral or pharmacological treatment ;
  • interest in quitting smoking; (9) have availability to attend sessions.

Exclusion Criteria

  • enrolled in another cessation program,
  • do not speak and read English,
  • do not have access to transportation by car or bus to attend sessions,
  • do not have childcare during session times,
  • have contraindications for patch use (pregnant/breastfeeding),
  • if they are in treatment for substance abuse (e.g., illicit drugs, alcohol abuse),
  • if they endorse active addiction to another substance (e.g., illicit drugs or alcohol),
  • if they have been diagnosed with an acute cardiac or respiratory condition;
  • people identified as having a severe mental illness

Outcomes

Primary Outcomes

7-day point prevalence abstinence

Time Frame: Overall effect at 12-months

Generalized linear mixed model of overall intervention effect.

Secondary Outcomes

  • 7-day point prevalence abstinence(6-months)

Study Sites (1)

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