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N/A N=1,865 Randomized Single-blind Treatment

'Questions About Quitting' Smoking Cessation Trial

Smoking

Enrolled (actual)
1,865
Serious AEs
0.0%
Results posted
Aug 2014
Primary outcome: Primary: Smoking Abstinence — 13.0; 13.8; 14.5; 13.3 percentage of abstinent participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Message Tone (Behavioral); Navigation (Behavioral); Proactive Outreach (Behavioral); Testimonials (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Kaiser Permanente
Primary completion
Nov 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Smoking Abstinence
13.0; 13.8; 14.5; 13.3; 14.5; 13.6
PRIMARY
Treatment Utilization for Smoking Cessation
26.1; 25.3; 26.0; 23.7; 25.8; 26.6

Summary

The current study tested the effectiveness of four potentially important tailoring factors (decisional framework, self-efficacy, navigation autonomy, and proactive outreach) in the context of an online motivational intervention for smoking cessation. A fifth factor was originally planned by dropped during intervention development due to confounds with the other planned factors. Information learned from this study will inform how to best design an online interventions for smoking cessation. Participants were recruited from a large, regional U.S. health plan. Using a full factorial design to screen for important main effects and 2-way interactions, participants were randomized to receive one of 16 different experimental factor combinations and followed for one year to assess program impact on smokers' use of empirically-validated cessation treatment and abstinence.

Eligibility Criteria

Inclusion Criteria

  • Member of Group Health Cooperative
  • Currently Smoking at Least 5 Cigarettes/Day
  • Access to Email and the Internet
  • Read and Write English
  • 18 years or older
  • Not currently receiving tobacco cessation treatment
  • Capable of participating in online and phone surveys

Exclusion Criteria

  • Persons will be excluded if they do not meet above criteria
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00992264). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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