Quit4Health Intervention in Supporting Smoking Cessation and Preventing Smoking Initiation in Young Adults

Authors
Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2018
PRIMARY OBJECTIVES: I. To evaluate whether smokers randomized to Quit4Health are more likely to quit smoking and remain tobacco‐free at 6 months than subjects randomized to the education only control group. II. To evaluate whether non‐smokers who are randomized to Quit4Health are less likely to initiate tobacco usage and remain tobacco‐free at 6 months than non‐smokers randomized to the education only control group. SECONDARY OBJECTIVES: I. To evaluate whether well‐established predictors of susceptibility and barriers to cessation (e.g. self‐efficacy, knowledge about associated risks, normative beliefs, attitudes, resistance skills, peer pressure) and recently identified predictors of tobacco use (e.g., depression, nicotine dependence, alcohol use, risk‐taking propensity) will mediate the effect of the intervention on both onset (for non‐smokers) and cessation (for smokers) of tobacco use. II. To evaluate whether, at the end‐of‐treatment (EOT) assessment, participants (both smokers and non‐smokers) in Quit4Health will report a significantly better perception of Quit4Health (message relevance, tailoring to specific needs based on tobacco use status, motivation to quit, etc.) compared with their counterparts in the education only control arm. OUTLINE: Participants are randomized to 1 of 2 groups. GROUP I: Participants utilize Quit4Health intervention that includes interactive features, coping strategies and games related to cigarettes and other tobacco products for 1 month. GROUP II: Participants read an educational booklet about cigarettes and other tobacco products for 1 month. After completion of study, participants are followed at 3 and 6 months.
Epistemonikos ID: b37ea01538bdbfccf186d7bad617b10bc27bacb7
First added on: May 22, 2024