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临床试验/NCT01484340
NCT01484340已完成不适用

A Smoking Cessation Trial in HIV-infected Patients in South Africa

Johns Hopkins University3 个研究点 分布在 1 个国家目标入组 560 人开始时间: 2014年3月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
560
试验地点
3
主要终点
Smoking Status Using a Point of Care Test for Measuring Carbon Monoxide (CO)

研究概览

简要总结

The purpose of this study is to conduct a randomized controlled trial (RCT) of intensive anti-smoking counseling plus nicotine replacement therapy versus intensive anti-smoking counseling alone among HIV-infected patients in South Africa, and to concurrently measure the prevalence of smoking among HIV-infected patients in South Africa.

详细描述

Tobacco use is estimated to be responsible for over 5 million deaths globally every year and HIV/AIDS kills 2 million worldwide, with persons living in the developing world especially at risk. However, the association between tobacco use and HIV is not clearly understood. The introduction of highly active antiretroviral therapy (HAART) has led to longer duration of survival following HIV-infection in the developed world, and now that HAART is being rolled out in the developing world, survival will increase in these highly endemic regions as well. Given this increase in survival, more people will die of non-HIV related illnesses for which smoking plays an important causal role. Smoking cessation for HIV-infected persons has been studied in the US though these studies have had small numbers and limited follow-up. US based studies suggest that approaches that combine nicotine replacement therapy (NRT) and counseling interventions are most successful. Optimal approaches in resource-limited settings have not been determined.

This study will compare intensive counseling plus NRT versus intensive counseling only, comparing smoking cessation at 2, 6 and 12 months. At 6 months, patients who are still current smokers will be given a second opportunity to receive their group assigned intervention, either intensive counseling plus NRT or intensive counseling alone. We will relate smoking exposure and cessation to HIV progression as measured by immunologic and viral markers, risk of respiratory infections, including tuberculosis, and AIDS-related malignancies. The RCT will be performed at the Tshepong HIV Wellness Clinic in Klerksdorp, South Africa, associated with the Reproductive Health & HIV Research Unit of the University of the Witwatersrand, South Africa.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Current, daily smoker (biochemically verified via a positive result on the SmokeScreen® test from GFC Diagnostics Ltd., as described in the outcomes)
  • Be willing to set a quit date within 2 weeks after baseline assessment
  • Agree to participate in study and anticipated to be attending Tshepong Wellness Clinic, Jouberton Community Health Center, or Grace Mokhomo Community Health Center (due to HIV infection) for at least 6 months

排除标准

  • Pregnant or nursing
  • Currently using smokeless tobacco (including electronic cigarettes, NRT or other cessation treatment)
  • Tuberculosis confirmed case
  • Weight <45 kg or BMI <20
  • Suffering from any unstable medical condition which could preclude use of the nicotine patch:
  • unstable angina
  • uncontrolled hypertension
  • active skin disease (e.g. psoriasis)
  • history of skin allergy

研究组 & 干预措施

Counseling only

Experimental

Participants in this arm will receive advice to quit smoking and self-help materials from the study interventionist in a standardized fashion (intensive anti-smoking counseling).

干预措施: Intensive Counseling (Behavioral)

Nicotine Replacement Therapy +counseling

Experimental

Participants in this arm will receive the nicotine patch in addition to the intensive anti-smoking counseling. Participants will receive instruction on proper use of the nicotine patch (i.e., placement, use of one patch a day, importance of not smoking while using the patch, and tapering of patches).

干预措施: Nicotine (Drug)

Nicotine Replacement Therapy +counseling

Experimental

Participants in this arm will receive the nicotine patch in addition to the intensive anti-smoking counseling. Participants will receive instruction on proper use of the nicotine patch (i.e., placement, use of one patch a day, importance of not smoking while using the patch, and tapering of patches).

干预措施: Intensive Counseling (Behavioral)

结局指标

主要结局

Smoking Status Using a Point of Care Test for Measuring Carbon Monoxide (CO)

时间窗: 6 months from baseline

A point of care test for measuring carbon monoxide (CO) will be conducted via the piCO Smokerlyzer from OPS Medical, designed specifically for smoking cessation programs and tobacco control programs. Carbon monoxide will be measured in an exhaled breath in parts-per-million (ppm). A reading of ≤ 7ppm will indicate abstinence.

Smoking Status Using a Point of Care Test for Measuring Cotinine

时间窗: 6 months from baseline

A point of care urine test for measuring cotinine will also be conducted via the SmokeScreen® test from GFC Diagnostics Ltd. to verify smoking status. A reading of \< 0.4 μg/ml cotinine equivalent will indicate abstinence.

次要结局

  • Smoking Status (COppm)(12 months from baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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