- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00503230
Reducing Ethnic Health Disparities: Motivating HIV+ Latinos to Quit Smoking (AURORA)
May 2, 2013 updated by: Butler Hospital
The purpose of this study is to develop and evaluate a brief clinic-based culturally tailored smoking cessation treatment for a largely low-income, Latino, HIV+ population.
We will compare this Culturally-Tailored Intervention (CTI) that incorporates a strong social support component and is targeted to the special needs and concerns of a Latino population to a Standard Care Intervention (SCI) control condition, in a randomized controlled trial.
We hypothesize that those Latinos receiving the CTI will demonstrate greater biochemically verified smoking abstinence rates at 12-months post-baseline than those receiving the SCI control treatment.
All study participants and their participating social supports will be offered use of the nicotine patch.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Advances in the treatment of HIV-disease have shown dramatic effects on improving immune function in a significant proportion of people infected with HIV in the United States.
For the first time since the beginning of the HIV epidemic, individuals with HIV are faced with the prospect of living longer, healthier lives.
Cigarette smoking is highly prevalent among HIV+ individuals and, in addition to the negative health consequences commonly resulting from smoking, poses unique health risks to those with HIV.
Our present research investigation, Positive PATHS (PATHS), the only NIH-funded smoking cessation study in HIV+ persons, is designed to evaluate a clinic-based motivational smoking cessation intervention among HIV+ smokers in Southern New England.
Preliminary analysis of the PATHS investigation indicate that both a standard care intervention (brief advice and NRT) and a more extensive motivational counseling condition have similar biochemically verified smoking abstinence rates 6-months post intervention, with Latino participants responding better to the brief standard care condition.
The goal of the current application is to expand upon the preliminary results of this study and target the standard care intervention to Latino HIV+ patients who were found to respond best to a brief directive approach.
This expanded standard care approach will incorporate the use of culturally specific materials to provide brief advice to both the patient and a patient-identified social support person who will be trained in ways to support cessation efforts.
Latinos are a population greatly affected by HIV and tobacco use, yet rarely discussed in existing research.
Most tobacco research that includes Latinos has focused on prevention efforts.
The few culturally specific cessation interventions that have been done have focused mostly on Mexicans in the Southwest and California1,2,3.
Considering the diversity of the Latino population in the US, those interventions may not generalize to Latinos in the Northeast, who are mostly of Puerto Rican and Dominican origin.
Research is limited in the area of HIV among Latinos and there are no studies to date that address the problem of tobacco use among HIV+ Latinos.
We propose to address this disparity by focusing this particular research study on Latino men and women living with HIV/AIDS.
Study Type
Interventional
Enrollment (Actual)
400
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Massachusetts
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Lowell, Massachusetts, United States, 01854
- Lowell Community Health Center
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New Bedford, Massachusetts, United States, 02740
- Greater New Bedford Community Center
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Roxbury, Massachusetts, United States, 02129
- Dimock Community Health Center
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Worcester, Massachusetts, United States, 01610
- Family Health Center of Worcester
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New York
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Bronx, New York, United States, 10467
- Montefiore Medical Center
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Rhode Island
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Providence, Rhode Island, United States, 02906
- Butler Hospital
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Providence, Rhode Island, United States, 02903
- Rhode Island Hospital HIV Clinic
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Providence, Rhode Island, United States, 02906
- The Miriam Hospital Immunology Clinic
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Be receiving care for HIV at one of the participating immunology clinics
- Self-identify as being Latino/Hispanic (defined as being 1st, 2nd or 3rd generation from any of the Spanish-speaking countries of North America, Central America, South America and the Caribbean).
- Be 18 years old or older.
- Be current smokers of cigarettes (past 7 days)
- Speak English or Spanish
Exclusion Criteria:
- Are pregnant or nursing
- Have uncontrolled hypertension
- Use other forms of tobacco like cigars or chewing tobacco or are using anything else to help them quit smoking
- Are allergic to the nicotine patch or have a skin condition like eczema or psoriasis that makes them unable to use the patch
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Standard Care Intervention (SCI)
|
Standard Care Intervention (SCI)
|
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Active Comparator: Culturally Tailored Intervention (CTI)
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Culturally Tailored Intervention (CTI)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Smoking Cessation
Time Frame: 6 and 12 months
|
6 and 12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Cassandra Stanton, Ph.D., Butler Hospital/Brown University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2005
Primary Completion (Actual)
July 1, 2011
Study Completion (Actual)
July 1, 2011
Study Registration Dates
First Submitted
July 17, 2007
First Submitted That Met QC Criteria
July 17, 2007
First Posted (Estimate)
July 18, 2007
Study Record Updates
Last Update Posted (Estimate)
May 3, 2013
Last Update Submitted That Met QC Criteria
May 2, 2013
Last Verified
May 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01DA018079 (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.