- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01811628
Project Impact: A Culturally-Tailored Adherence Intervention for Latino Smokers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
If participant decides to take part in this study, they will complete a questionnaire about themselves (such as their age, preferred language, and education level) and their smoking habits. This questionnaire should take about 10-15 minutes to complete.
After participant completes this questionnaire, they will be interviewed by a researcher. During this interview participant will be asked to discuss a variety of topics related to smoking and quitting, such as their experience with attempts to quit smoking and problems they may have had. This interview will last about 1 hour.
The interview will be audio-recorded. Participant's interview answers will later be transcribed (written down) without their name or any other identifying information.
Study participation will be complete after the interview.
This is an investigational study.
Up to 48 people will be enrolled in this study. All will take part at MD Anderson.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Texas
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Houston, Texas, United States, 77030
- University of Texas MD Anderson Cancer Center
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- 18+ years of age
- Current smoker (>10 cigarettes per day for the past 3 months) or recently quit Smoking (within the past year) but has not smoked for the past 2 months)
- Read, understand and speak Spanish
- Identify as being of Latino (or Hispanic) heritage, ethnicity, or ancestry.
Exclusion Criteria:
- The self-report of a diagnosis of Schizophrenia, Delusional Disorder, Schizoaffective Disorder or Bipolar Disorder in the past year.
- The self-report of a diagnosis of a Substance Dependence Disorder other than Nicotine in the past year (i.e., Alcohol Dependence, Amphetamine Dependence, Cannabis Dependence, Cocaine Dependence, Hallucinogen Dependence, Inhalant Dependence, Opioid Dependence, Phencyclidine Dependence, Sedatives, Hypnotics, or Anxiolytic Dependence, or Polysubstance Dependence)
- Unavailable for a 1.5 hour visit to MD Anderson Cancer Center.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Questionnaire + Interview
Latinos and Hispanics who are smokers and recent quitters.
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Questionnaire completion taking about 10-15 minutes.
Other Names:
Audio-recorded interview that will last about 1 hour.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Information Collection From Latino and Hispanic Smokers or Recent Quitters
Time Frame: 1 day
|
Primary aim of this study is to conduct in-person qualitative interviews with 48 Latino smokers or recent quitters in order to gather information regarding potential elements to include in a future intervention that will target smoking cessation treatment adherence among Latino smokers. This exploratory and qualitative study will utilize thematic analyses of interview discussions to analyze and derive elements that will ultimately be included in a treatment manual. Data analyzed using thematic analysis, enabling recurring themes from the data presented and discussed and opposing cases highlighted. Analyses facilitated by the use of N*Vivo - a software package package specific to qualitative research. A qualitative analyses of the content of the qualitative interviews conducted separately for current smokers and recent quitters. |
1 day
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Marcel A. de Dios, PHD, M.D. Anderson Cancer Center
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2012-1051
- K01CA160670 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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