Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
706 participants
INTERVENTIONAL
2004-01-31
2015-04-30
Brief Summary
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Detailed Description
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If you are found to be eligible, you will be enrolled in this study and asked to complete an interview that should last about 1 hour. During this interview, you will be asked basic questions, such as your age, education level, and smoking history. You will also be asked questions about your mood, quality of life, and stress. You will then be asked to complete a short test that involves completing some basic tasks, such as remembering several words and drawing a simple shape. This test, which will take about 2-5 minutes to complete, is used to measure attention and concentration.
You will then be randomly assigned (as in the toss of a coin) to one of two treatment groups. There is an equal chance of being assigned to either group.
If you are assigned to Group 1, you will receive advice from your physician/provider to stop smoking and written materials designed to help you quit smoking.
If you are assigned to Group 2, you will receive the advice from your physician/provider to quit smoking and the written materials, but you also be given a cell phone and be called 11 times over the course of an 12 to 13 week period. During these calls, which will last about 10 minutes, you will be asked to talk about smoking and quitting smoking. Access to a hotline number that you can call to speak with a counselor about quitting smoking will also be given to you if you are assigned to group 2. Participants in Group 1 will not get the number to the hotline. There is a limited number of prepaid minutes on the phone, so participants who receive a cell phone should make an effort to save enough minutes to complete this study.
You will be asked to complete three more interviews about 3-, 6-, and 12-months after the first interview. During these interviews, you will again be asked questions about your smoking behavior, mood, quality of life, and stress. All three of these interviews will take about one hour to complete. Your participation in this study will be complete after the 12-month interview.
Lost, stolen, or broken cell phones will not be replaced, but participants will remain on study.
This is an investigational study. Up to 705 participants will take part in this research study. All participants will be enrolled at Thomas Street Clinic.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Recommended Standard of Care
Recommended Standard of Care (RSOC) = Physician Advice + Written Materials
Recommended Standard of Care
Advice from your physician to stop smoking and written materials designed to help you quit smoking.
RSOC + Cell Phone Intervention
Recommended Standard of Care (RSOC) + Cell Phone Intervention
Cell Phone Intervention
Study participants called on a cell phone 11 times over course of a 12 - 13 week period, during 10 minute calls questions asked about smoking and quitting smoking.
Recommended Standard of Care
Advice from your physician to stop smoking and written materials designed to help you quit smoking.
Interventions
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Cell Phone Intervention
Study participants called on a cell phone 11 times over course of a 12 - 13 week period, during 10 minute calls questions asked about smoking and quitting smoking.
Recommended Standard of Care
Advice from your physician to stop smoking and written materials designed to help you quit smoking.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. 18 years of age or older
3. Current, regular smoker (\> 5 cigarettes per day for the past 30 days, breath CO of \> 7ppm)
4. English or Spanish speaking
5. Able to provide written informed consent to participate
6. Willing to set a quit date within 1 week of baseline assessment
Exclusion Criteria
2. Current participation in another smoking cessation program
18 Years
ALL
No
Sponsors
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National Cancer Institute (NCI)
NIH
M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Damon Vidrine, MS, DRPH, BA
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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Thomas Street Clinic
Houston, Texas, United States
University of Texas MD Anderson Cancer Center
Houston, Texas, United States
Countries
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References
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Mdege ND, Shah S, Dogar O, Pool ER, Weatherburn P, Siddiqi K, Zyambo C, Livingstone-Banks J. Interventions for tobacco use cessation in people living with HIV. Cochrane Database Syst Rev. 2024 Aug 5;8(8):CD011120. doi: 10.1002/14651858.CD011120.pub3.
Buchberg MK, Gritz ER, Kypriotakis G, Arduino RC, Vidrine DJ. The role of BMI change on smoking abstinence in a sample of HIV-infected smokers. AIDS Care. 2016;28(5):603-7. doi: 10.1080/09540121.2015.1120854. Epub 2015 Dec 15.
Related Links
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University of Texas MD Anderson Cancer Center Website
Other Identifiers
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NCI-2012-02109
Identifier Type: REGISTRY
Identifier Source: secondary_id
2003-0784
Identifier Type: -
Identifier Source: org_study_id
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