MedPath

Feasibility and Efficacy of a Brief Mindfulness-Based Intervention SMOKING INTERVENTION VIA THE INTERNET

Not Applicable
Completed
Conditions
Substance Use
Smoking Reduction
Interventions
Behavioral: Control Intervention
Behavioral: Mindfulness Intervention
Registration Number
NCT04572126
Lead Sponsor
Wayne State University
Brief Summary

The current study will examine both the feasibility and efficacy of a single session, web-based mindfulness-based intervention for smoking cessation. The study will explore (1) participants' subjective experiences of the intervention, (2) cravings and negative affect both before and after the intervention, and (3) changes in tobacco use one week and one month following the initial intervention. Further, the study will examine how often participants utilize the intervention between the initial study and follow-up periods.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
Inclusion Criteria
  • Daily Smoker
  • Has a desire to quit or reduce smoking.
  • Is not currently involved in another smoking reduction or cessation program.
Exclusion Criteria

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control GroupControl InterventionParticipants in the control group will receive instructions to cope with cravings how they normally would.
Mindfulness GroupMindfulness InterventionParticipants in the mindfulness group will receive mindfulness based instructions.
Primary Outcome Measures
NameTimeMethod
Change in Cigarette/E-cigarette CravingImmediately preceding and following intervention.

Craving to smoke will be measured using the 10-item Brief Questionnaire of Smoking Urges (Cox, Tiffany, \& Christen, 2001).While the QSU-brief can be scored by using all 10 items for one total craving score, maximum likelihood factor analysis of the QSU-brief revealed a two-factor model consisting of (1) a strong desire and intention to smoke with the perception of receiving positive rewards from smoking and (2) the expectation that smoking would relieve negative affect and the strong desire to smoke. The measure will be administered immediately preceding and following the intervention to show intervention influence on craving.

Change in Past Month Cigarette and E-Cigarette use.Immediately before the intervention and at one-month follow-up.

An online version of the TLFB (Sobbel \& Sobbel, 1992) will be used to measure past-month cigarette and e-cigarette use. The measure will be administered pre-intervention and one-month following the intervention to show change over time.

Change in Positive and Negative AffectImmediately preceding and following intervention as well as at one-month follow-up.

Positive and negative affect will be measured by the Positive and Negative Affect Schedule (Watson \& Clark, 1999).

Subjective Ratings QuestionnaireImmediately post-intervention

The participant's ratings of subjective likeability and helpfulness of the intervention. These ratings will be measured on a 5-point Likert Scale with higher scores representing more likeability and helpfulness. The 11-item questionnaire results in a score ranging from 11-55.

Secondary Outcome Measures
NameTimeMethod
Intervention Use.One-month after intervention.

Number of times participants viewed intervention between intervention completion and one-month follow-up.

Trial Locations

Locations (1)

Wayne State University

🇺🇸

Detroit, Michigan, United States

© Copyright 2025. All Rights Reserved by MedPath