Squiers 2017.
Methods |
Study design: RCT Country: USA Recruitment: online advertising and search ads via Facebook, Craigslist, Pandora, and Google, Yahoo! and Bing, plus email recruitment via market research panels Study dates: 2013‐14 |
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Participants |
Baseline characteristics (n = 4027)
Inclusion criteria: aged 18‐29 years. Reside in the USA. Smoke cigarettes at least 5 days/month. Be interested in quitting cigarette use. Not be involved in a cessation programme. Have an active email account. Be able to receive text messages on their mobile phone. Be the only member of your household participating in this study. Be willing to share contact information with the study team in order to share information about the study on a timely basis. Exclusion criteria: didn't complete baseline survey. The anti‐fraud process included automated duplication checks of phone numbers, email addresses, and IP addresses. If duplicates were detected, the individual was excluded from the study. Failure to provide informed consent. Refused the honesty pledge. Faced technical difficulties (e.g. undelivered text messages). Texted “STOP” at any point before their QD. Opted out of the study entirely by notifying the project team, typically via email |
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Interventions |
Arm 1: periodic cessation assessments and QD reminder messages (total 11 messages) Arm 2: arm 1 messages above, plus motivational preparatory messages for 2 weeks prior to participants’ QD (total 40 messages) Arm 3: all of the messages from Arms 1 and 2 above, plus 6 weeks of follow‐up post‐QD messages (total 127 messages) |
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Outcomes | Definition of abstinence: self‐reported 7‐day repeat point prevalence abstinence at 32 weeks | |
Funding source | National Institutes of Health, National Cancer Institute HHSN261201400002B, HHSN26100006, HHSN26100007 | |
Conflicts of interest | None | |
Notes | We split Arm 1 and compared it with arms 2 and 3 in the comparison of higher‐ versus lower‐frequency text messaging | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Insufficient information about the sequence generation process |
Allocation concealment (selection bias) | Low risk | Not stated but as all done online it is very unlikely to have any bias |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Minimal contact with investigators |
Incomplete outcome data (attrition bias) All outcomes | Low risk | There was a 64.4% response rate overall. Arm 1: 846/1313; Arm 2: 933/1400; Arm 3: 824/1314. ITT analysis |