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Completed

NCT Number: NCT02982772

Patch Study - Intervention for HIV Positive Smokers

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Miami

Miami, Florida, 33136, United States

About this study

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).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HIV infected smokers
  • 18 years of age and older
  • Fluent in English or Spanish
  • Able to consent
  • Ready to quit smoking

Exclusion criteria

  • Psychotic or disabling psychiatric disorders
  • Six months post-myocardial infarction or stroke
  • Diabetes requiring insulin
  • Treatment for vascular problems
  • Non-treated hypertension,
  • Severe liver or kidney disease
  • History of allergies to the nicotine patches
  • Severe eczema or psoriasis
  • Temporal-mandibular joint disease or dental appliances
  • Pregnant women or women that are breastfeeding
  • Subjects participating in other interventions/research

Treatment and study plan

Combination Therapy

Other

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

Standard Care Intervention

Other

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

Primary outcomes

  1. Rates of Smoking Cessation

    Time frame: 3 months

    verified continuous abstinence (carbon monoxide < 10ppm and cotinine <15 ng/mL).

  2. Rates of Smoking Cessation

    Time frame: 6 months

    verified continuous abstinence (carbon monoxide < 10ppm and cotinine <15 ng/mL).

  3. Rates of Smoking Cessation

    Time frame: 12 months

    verified continuous abstinence (carbon monoxide < 10ppm and cotinine <15 ng/mL).

Secondary outcomes

  1. Change in Clinical Outcomes

    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:

    • CD4 (counts and percentage).
    • HIV Viral load (logs).
    • Vital signs (Blood pressure in mm Hg, breaths per minute, beats per minute).
    • Anthropometric measures [Body Mass Index = weight(kilograms) / height(meters2), Waist and hip circumference in inches].
    • In health-related quality of life measured as changes in the total score of Health-Related Quality of Life survey.

    Scale Title: Smoking Cessation Quality of Life (SCQoL) - Physical subscale Minimum 9, maximum 27 (higher scores=worse outcome)

  2. Number of Participants With Verified Continuous Abstinence

    Time frame: 3 months

    Verified continuous abstinence using a breathalyzer carbon monoxide < 10ppm

  3. Prevalence of Side Effects-safety

    Time frame: Baseline-6 months

    Total number of self reported side effects from Baseline through 6 months.

  4. Change in Clinical Outcomes

    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:

    • CD4 (counts and percentage).
    • HIV Viral load (logs).
    • Vital signs (Blood pressure in mm Hg, breaths per minute, beats per minute).
    • Anthropometric measures [Body Mass Index = weight(kilograms) / height(meters2), Waist and hip circumference in inches].

    Scale Title: Smoking Cessation Quality of Life (SCQoL) - Physical subscale Minimum 9, maximum 27 (higher scores=worse outcome)

    • In health-related quality of life measured as changes in the total score of Health-Related Quality of Life survey.
  5. Number of Participants With Verified Continuous Abstinence

    Time frame: 6 months

    verified continuous abstinence using a breathalyzer carbon monoxide < 10ppm

  6. Number of Participants With Verified Continuous Abstinence

    Time frame: 12 months

    verified continuous abstinence using a breathalyzer carbon monoxide < 10ppm

  7. Prevalence of Side Effects-safety

    Time frame: 6 through 12 months

    Total number of self reported side effects from 6 through 12 months.

Sponsors and collaborators

Lead sponsor

dr. maria miguez

Other

Collaborators

  • University of Miami

Registry information

Official study title

Biobehavioral Intervention for Smokers Living With HIV (Human Immunodeficiency Virus)

Important dates

Study start
2016
Primary completion
2021
Study completion
2021
First posted
Dec 5, 2016
Registry last updated
Oct 6, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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