跳至主要内容
临床试验/NCT01570595
NCT01570595已完成1 期

A Pilot Study of Positively Smoke Free on the Web (PSFW) for HIV-infected Smokers

Georgetown University2 个研究点 分布在 1 个国家目标入组 138 人开始时间: 2011年9月最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
138
试验地点
2
主要终点
24-hour Point-prevalence tobacco abstinence

研究概览

简要总结

The purpose of this study is to evaluate the first web-based cessation program developed expressly for people living with HIV who smoke tobacco. Main study goals are (1) to evaluate the website's feasibility (i.e., recruitment, adherence, retention, and satisfaction) and (2) to complete a prospective, randomized controlled trial comparing the efficacy of the online program to standard care with a primary outcome of 3 month point-prevalence abstinence.

详细描述

Positively Smoke Free on the Web is the first web-based cessation program developed expressly for people living with HIV (PLWH) who smoke tobacco. It is a resource that is ready for clinical use, but its feasibility and efficacy have yet to be studied. Main study goals are (1) to evaluate the website's feasibility (i.e., recruitment, adherence, retention, and satisfaction) in a cohort of 69 PLWH smokers, and (2) to complete a prospective, randomized controlled trial comparing the efficacy of the online program to standard care (total N = 138) with a primary outcome of 3 month point-prevalence abstinence.

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

  • Laboratory confirmation of HIV infection
  • Montefiore Medical Center Infectious Disease Clinic patient
  • Current tobacco user
  • Affirmed motivation to quit within the next 6 months
  • Have home access to the Internet
  • Read above 4th grade level (by REALM)
  • Willingness to grant informed consent and undergo randomization

排除标准

  • Pregnant or breastfeeding women
  • People with contraindications to nicotine replacement therapy
  • People currently receiving other tobacco treatment
  • Spouses, partners, and/or roommates of current study participants

研究组 & 干预措施

Standard Care

Active Comparator

This group will receive "standard care" for their smoking, including advice to quit, a quit-smoking brochure, and an offer of three months of nicotine replacement therapy (nicotine patches).

干预措施: Web-Based Tailored Smoking Cessation Intervention (Behavioral)

Web-Based Intervention

Experimental

This group will be asked to participate in the online quit smoking program. At their first visit, they will be given an ID number to log in to the quit smoking program, and they will complete their first log in with the research assistant. The online program is made up of 8 separate online sessions that are supposed to be completed approximately once per week. Each sessions is written to take an average reader 15-30 minutes to complete. The entire program is meant to be completed in 7 weeks. At the first visit, participants are asked to provide an email address and/or cell phone number so reminders can be sent, by email or text message, to complete the sessions. If participants are late completing a session, they may receive call from clinic staff as a reminder.

干预措施: Web-Based Tailored Smoking Cessation Intervention (Behavioral)

Standard Care

Active Comparator

This group will receive "standard care" for their smoking, including advice to quit, a quit-smoking brochure, and an offer of three months of nicotine replacement therapy (nicotine patches).

干预措施: Standard of Care (Behavioral)

结局指标

主要结局

24-hour Point-prevalence tobacco abstinence

时间窗: 3 months

The proportion of each group achieving 24-hour point prevalence abstinence at Visit 3 (i.e., abstinence on or around Day 121 - 3 months post-Quit Day in the Intervention condition) by exhaled carbon monoxide, an accepted method for biochemical validation of abstinence.

次要结局

  • Degree of Participation in Intervention (Feasibility)(3 Months (duration of intervention))
  • Knowledge and Behavior Change(Day 0, 42, 121)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验