Online Lapse Management Intervention
NCT03191825 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1500
Last updated 2021-10-08
Summary
The purpose of the trial is to test the adjunctive effect of adding a lapse management system to a best practices web- and mobile smoking cessation program.
Conditions
- Nicotine Dependence, Cigarettes
Interventions
- OTHER
-
Endre: a digital smoking cessation counsellor
A comprehensive 25-session intervention delivered by web, e-mail and SMS-text messages. Sessions are released one each day for 18 days, and then every second day for 14 days. Intervention content is tailored based on user input and individual usage pattern. The intervention is described in detail in Holter, Johansen \& Brendryen (2016). How a fully automated eHealth program simulates three therapeutic processes: A case study. Journal of Medical Internet Research 18 (6).
- OTHER
-
Lapse management system triggered from web-page
The lapse management system is based on a day-to-day logging of the target behavior (smoking). This logging goes on for four weeks after an initial quit attempt. The current version of the system logs by asking the participant about their smoking status every time they log on to "Endre" (the digital smoking cessation counsellor). Participants that report a lapse is routed to a fully automated counselling session delivered by web.
- OTHER
-
Lapse management system triggered by SMS-textmessage
The lapse management system is based on a day-to-day logging of the target behavior (smoking). This logging goes on for four weeks after an initial quit attempt. The current version of the system logs by asking the participant about their smoking status in a textmessage (SMS) sent each evening. Participants that report a lapse, receives a new SMS with a link to a fully automated counselling session delivered by web.
Sponsors & Collaborators
-
The Research Council of Norway
collaborator OTHER -
Charles University, Czech Republic
collaborator OTHER -
University of Oslo
lead OTHER
Principal Investigators
-
Håvar Brendryen, PhD · University of Oslo
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-09-12
- Primary Completion
- 2022-10-01
- Completion
- 2022-10-01
Countries
- Czechia
- Norway
Study Locations
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