The primary goal of this study is to use qualitative interviews and focus groups to aid us in adapting a face-to-face smoking cessation intervention for delivery through text messaging. After design is completed, the intervention will be pilot tested with a sample of young adults (ages 18-35) who smoke. Final assessments will be conducted at 7 weeks (end of treatment) and both 3 and 6 month follow up.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
84
A 7-week program of daily text messages
non-smoking related text messages will be given on the same daily schedule as matches the active intervention to establish a control for contact time.
The Miriam Hospital
Providence, Rhode Island, United States
Smoking abstinence
7-day point prevalence abstinence will be measured at 6 months post-treatment.
Time frame: Six months post-treatment
Usability and Acceptability of the intervention
Usability and acceptability of the intervention will be assessed at the end of treatment (week 7).
Time frame: 7 weeks (end of treatment)
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