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Tobacco Status Project: Social Media Intervention for Young Adult Smokers

Not Applicable
Completed
Conditions
Smoking
Interventions
Behavioral: Facebook intervention
Behavioral: Smokefree.gov
Registration Number
NCT02207036
Lead Sponsor
University of California, San Francisco
Brief Summary

This randomized clinical trial will test the efficacy of a Facebook intervention based on the Transtheoretical Model (Prochaska and DiClemente) and US Public Health Service Clinical Practice Guidelines with young adults who smoke cigarettes who are age 18 to 25 (N=480).

Detailed Description

Participants will be randomized to one of two conditions: (1) a Facebook-delivered intervention tailored to readiness to quit smoking; or (2) the control condition (referral to the Smokefree.gov website). The intervention will include 12 weeks of Facebook-based messages and activities tailored to participants' stage of change.

Assessments will occur at baseline, 3, 6, and 12 months follow-up. Assessments will include measures on smoking patterns and thoughts about abstinence. All participants who report no past 7-day smoking will be asked to give biochemical verification of smoking status with saliva cotinine test kits that will be mailed to participants.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
501
Inclusion Criteria
  • ages 18-25 years old
  • english literate
  • have access to Smartphone or computer with camera
  • indicate they go on Facebook "most" (≥ 4) days per week
  • have smoked ≥100 cigarettes in their lives and currently smoke at least 1 cigarette per day on 3 or more days of the week
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Exclusion Criteria
  • do not read English
  • younger than 18 or older than 25 years of age
  • do not have access to a Smartphone or computer with a camera
  • only go on Facebook 3 or fewer days a week
  • have smoked less than 100 cigarettes in their lifetime or do not currently smoke at least 1 cigarette per day on 3 or more days of the week
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Facebook interventionFacebook interventionAssignment to private group on Facebook with 3 months of content delivered to the group.
ReferralSmokefree.govReferral to smokefree.gov website
Primary Outcome Measures
NameTimeMethod
7-day point prevalence abstinence at 3 months3 months post baseline

Reports of no smoking in the 7 days prior to the 3 month assessment. Biochemical verification of abstinence will also be recorded.

7-day point prevalence abstinence at 6 months6 months post baseline

Reports of no smoking in the 7 days prior to the 6 month assessment. Biochemical verification of abstinence will also be recorded.

7-day point prevalence abstinence at 12 months12 months post baseline

Reports of no smoking in the 7 days prior to the 12 month assessment. Biochemical verification of abstinence will also be recorded.

Secondary Outcome Measures
NameTimeMethod
Reduction in cigarettes smoked by at least 50% between Baseline and each follow-up timepoint3, 6, and 12 months post baseline

Reduction will be assessed at 3, 6, and 12 month follow-ups.

Quit attempts3, 6, and 12 month post-baseline

Quit attempt during the follow-up period at 3, 6, and 12 months post-baseline.

Trial Locations

Locations (1)

University of California San Francisco Department of Psychiatry

🇺🇸

San Francisco, California, United States

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