Mobile Text Messaging as an Adjunct Function to an Internet-based Smoking Cessation Intervention Implemented in the General Population and in a Health Care Setting
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 4,300
- 试验地点
- 1
- 主要终点
- Comparison of the percentage of abstinent people between the arms of the trial,1,3,6 and 12 months after self-reported smoking cessation date
研究概览
简要总结
The purpose of the study is to investigate the effectiveness of a smoking cessation intervention delivered through a technological web based platform (www.slutta.no) with or without a supportive SMS function.
详细描述
The study has two arms and are conducted in Norwegian. Users who registered with a new username on www.slutta.no, after study start May 12th 2010 and before November 1st 2012, are eligible. All phases of the trial, from randomization and informed consent procedures to data collection, are automated and conducted online. The following inclusion criteria are used: age 16 years or older, access to a mobile phone with a Norwegian phone number and they must submit an informed consent form.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 16 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •(all arms):
- •Aged 16 and older
- •Current smoker: Willing to quit smoking within the next 12 weeks
- •Former smokers; Having quit smoking within the previous six months
- •Having a regular access to Internet
- •Having a personal e-mail address
- •Having a personal mobile cell phone with a Norwegian number
- •Given informed consent
- •Can read and understand Norwegian
- •Reporting no association with the University Hospital of North Norway (arm1&2)
- •Reporting an association with the University Hospital of North Norway (arm3&4)
排除标准
- •Less than 16 years of age
- •No personal e-mail address
- •No personal mobile cell phone
- •Not able to give the informed consent
研究组 & 干预措施
Internet-based coaching .
Arm 1. Those in the "active comparator arm" will benefit from automated internet-based coaching. The subjects will be recruited from the general population reporting not to be associated with the University Hospital of North Norway and randomized to arm 1 or 2.
干预措施: Internet-based behavioral coaching (Device)
SMS based coaching
Arm 2. The subjects will receive automated "coaching"by SMS.The subjects will be recruited from the general population reporting not to be associated with the University Hospital of North Norway and randomized to arm 1 or 2.
干预措施: SMS based coaching (Device)
SMS coaching UNN recruited
Arm 3.The subjects will be recruited from those reporting to be associated with the University Hospital of North Norway and randomized to arm 3 or 4.
干预措施: SMS coaching - UNN recruited (Device)
Craving/Panic function. UNN recruited
Arm 4. The subjects will in addition to the automated "coaching"by SMS get a SMS panic/craving function. The subjects will be recruited from subjects reporting to be associated with the University Hospital of North Norway and randomized to arm 3 or 4.
干预措施: SMS craving function - UNN recruited (Device)
结局指标
主要结局
Comparison of the percentage of abstinent people between the arms of the trial,1,3,6 and 12 months after self-reported smoking cessation date
时间窗: 30 months after inclusion
The investigators will compare the percentage of smokers who successfully quit. Point prevalence abstinence will be measured (not smoking, event a puff, in the week preceding the questioning).
次要结局
- Comparison between the arms of the trial regarding visits, time logged in, used elements of the website and overall adherence period.(30 months after inclusion)
- 28 days of continuous smoking prevalence at 6 months after selfreported smoking cessation date(6 months after selfreported smoking cessation date)
- Comparison between the arms of the trial regarding satisfaction with website and mobile text messages at the time of the 4 questionnaires(30 months after inclusion)
- Selfreported involvement in any vehicle crashes during the last 6 months(6 months after selfreported smoking cessation date)