University of Miami
Miami, Florida, 33136, United States
NCT Number: NCT02982772
The overall objective of the transdisciplinary team of Human Immunology Virus (HIV) and Tobacco funded researchers is to test if tailoring nicotine replacement doses to temper these excessive levels will enhance the efficacy of the intervention. To test researchers proposed model 600 people living with HIV (PLWH) ready to quit smokers will be enrolled in a double-blind randomized clinical trial intent-to-treat design, comparing a standard well-validated brief smoking intervention, that following national guidelines + nicotine replacement therapy (NRT), versus the tailored one (brief smoking intervention + personalized doses of nicotine replacement therapy). The primary outcome for this study will be rates of smoking cessation, point prevalence abstinence (prior 7 and prior 30 days), and verified continuous abstinence 3-, 6-, and 12-months post scheduled quit day.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Miami, Florida, 33136, United States
The overall objective of the transdisciplinary team of Human Immunology Virus (HIV) and Tobacco funded researchers is to test if tailoring nicotine replacement doses to temper these excessive levels will enhance the efficacy of the intervention. This will be accomplished by assessing: 1) pre-trial plasma levels, 2) doing genotyping, which to researchers knowledge has not been used in cessation studies among people living with HIV (PLWH), and 3) providing tailored feedback to the participants, based on the assumption that the higher the knowledge and perception of risk, the higher the interest in modifying a risky behavior(s). To test researchers proposed model based in proven smoking prevention and control methods 600 PLWH ready to quit smokers will be enrolled in a double-blind randomized clinical trial intent-to-treat design, comparing a standard well-validated brief smoking intervention, that following national guidelines will consist on brief advice + nicotine replacement therapy, versus the tailored one (brief smoking intervention + personalized doses of nicotine replacement therapy (NRT). The primary outcome for this study will be rates of smoking cessation, point prevalence abstinence (prior 7 and prior 30 days), and verified continuous abstinence 3-, 6-, and 12-months post scheduled quit day. The knowledge gained here has the potential to provide a more complete bio-behavioral model to the intervention field. The proposed study if successful will provide a new tailored, replicable, and manual-based intervention for people living with HIV. It can also provide much need it information in regards to key mediators and moderators of smoking cessation interventions in this vulnerable population. Researchers long term goal is to reduce the burden of one of the most devastating causes of morbi-mortality in researchers time and improve their quality of life. The study could also pave the path to use a similar model to tailor smoking interventions for other populations (e.g., menthol users, older women, adolescents, older adults).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Brief behavioral intervention
The test product is a transdermal nicotine patch for 12 weeks. The dosage of the test product depends on the new algorithm (amount, addiction, prior attempts) Nicotine Gums for 12 weeks.
Other names: Nicoderm, Nicorette
Brief Behavioral Intervention
The test product is transdermal Nicotine replacement patch for 10 weeks.The dosage of the test product follows the product guidelines and depends on the amount of cigarettes used.
Standard Flavored Gums for 10 weeks
Time frame: 3 months
verified continuous abstinence (carbon monoxide < 10ppm and cotinine <15 ng/mL).
Time frame: 6 months
verified continuous abstinence (carbon monoxide < 10ppm and cotinine <15 ng/mL).
Time frame: 12 months
verified continuous abstinence (carbon monoxide < 10ppm and cotinine <15 ng/mL).
Time frame: 6 months
The investigators will analyze changes in the following parameters since baseline, and will be given one point for each parameter that improves:
Scale Title: Smoking Cessation Quality of Life (SCQoL) - Physical subscale Minimum 9, maximum 27 (higher scores=worse outcome)
Time frame: 3 months
Verified continuous abstinence using a breathalyzer carbon monoxide < 10ppm
Time frame: Baseline-6 months
Total number of self reported side effects from Baseline through 6 months.
Time frame: 12 months
The investigators will analyze changes in the following parameters since baseline, and will be given one point for each parameter that improves:
Scale Title: Smoking Cessation Quality of Life (SCQoL) - Physical subscale Minimum 9, maximum 27 (higher scores=worse outcome)
Time frame: 6 months
verified continuous abstinence using a breathalyzer carbon monoxide < 10ppm
Time frame: 12 months
verified continuous abstinence using a breathalyzer carbon monoxide < 10ppm
Time frame: 6 through 12 months
Total number of self reported side effects from 6 through 12 months.
dr. maria miguez
Other
Biobehavioral Intervention for Smokers Living With HIV (Human Immunodeficiency Virus)
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