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Clinical Trials/NCT03276767
NCT03276767
Unknown
Not Applicable

An RCT Comparing Reminders Sendt by SMS or by E-mail in an Online Smoking Cessation Intervention

University of Oslo2 sites in 2 countries700 target enrollmentSeptember 12, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nicotine Dependence Tobacco Product
Sponsor
University of Oslo
Enrollment
700
Locations
2
Primary Endpoint
Quit attempt
Last Updated
4 years ago

Overview

Brief Summary

The primary purpose of the current study is to compare the effect of SMS-textmessage vs e-mail reminders on user engagement and proportion of reported quit attempts in an online smoking cessation intervention.

Detailed Description

Web- and mobile phone health behavior change interventions, including smoking cessation programs, offer great promise, but little is known about how such interventions should be designed to increase user engagement. The primary purpose of the current study is to compare the effect of SMS-textmessage vs e-mail reminders on user engagement and proportion of reported quit attempts in an online smoking cessation intervention. The investigators propose a 2-arm RCT with 700 adult study participants that all receive a best practices web-based smoking cessation program designed for use on smart phones (web-app). The intervention includes a ten day preparation phase, in which participants continue smoking. On the eleventh day (and onward) the user will receive a session in which (s)he is asked whether (s)he has quit smoking or not. If not, the user will receive additional treatment sessions until (s)he reports having quit (or dropped out of the study). Each day (for up to 14 days) a new unique session is assigned to the user. However, if the user does not log on to the web-intervention and starts using the session by noon on the second day after assignment, the user will receive a reminder to do so. When a user is to be sent a reminder for the first time, (s)he will be randomized to either receive such reminders by SMS or by e-mail. The primary outcome is reporting a quit attempt or not. Secondary outcomes include number web-sessions started and completed and time spent navigating sessions after the first reminder is received.

Registry
clinicaltrials.gov
Start Date
September 12, 2017
End Date
October 1, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Håvar Brendryen

Senior Research Scientist

University of Oslo

Eligibility Criteria

Inclusion Criteria

  • 18 years or older
  • current smoker
  • determined to or considering to quit smoking
  • provide valid e-mail address
  • provide valid norwegian cell phone number
  • complete a baseline questionnaire
  • start using the intervention (pushing the next page button one time or more on the first session provided)
  • has not logged on to any of the online session within noon on the second day after that particular session was made available

Exclusion Criteria

  • Not starting the first treatment session
  • Taking every treatment session on time (no need for reminders, and thus not randomized)

Outcomes

Primary Outcomes

Quit attempt

Time Frame: Within 6 weeks after starting the first session of the intervention

User report a quit attempt

Secondary Outcomes

  • Number of sessions completed(Within 6 weeks after starting the first session of the intervention)
  • Number of sessions started after first reminder(Within 6 weeks after starting the first session of the intervention)

Study Sites (2)

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