Augustson 2017.
Methods |
Study design: RCT Country: China Recruitment: recruited from subscribers to Nokia Life Tools on Nokia phones in both urban and rural areas of China’s Zhejiang, Heilongjiang, and Shaanxi provinces Date of study: 2013 |
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Participants |
Baseline characteristics (n = 8000)
Inclusion criteria: Nokia Life Tools users; adult smokers Exclusion criteria: none specifically stated |
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Interventions |
High‐frequency text contact (HFTC): 91 messages during the 6 weeks; 3 messages/day for weeks 1 and 2, 2/day for weeks 3‐5, and 1/day for week 6. At the end of each text message, participants in both groups were offered the opportunity to cancel the service via text. The text messages provided encouragement, practical advice to help maintain cessation, and information on the health effects of smoking. Low‐frequency text contact (LFTC): 1 text message/week, for a total of 6 text messages during the 6‐week intervention period; a subset of text messages on smoking’s health effects |
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Outcomes | Definition of abstinence: 7‐day point prevalence abstinence self‐reported via text message at 6‐month follow‐up | |
Funding source | National Cancer Institute, National Institutes of Health, U.S. Dept of Health Human Services | |
Conflicts of interest | None declared | |
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Quote: "Intervention participants who opted into the phase 3 SC trial were randomly assigned to the intervention or comparison group (n ¼ 4000 in each group)" Therefore, participants were randomly assigned but it was not stated how |
Allocation concealment (selection bias) | Unclear risk | Not stated |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Outcome assessed by text message with no face‐to‐face contact Quote: "participants were not aware of the separate intervention arms and therefore did not know what group they were assigned to" |
Incomplete outcome data (attrition bias) All outcomes | High risk | Loss to follow‐up clearly stated but > 50%; 58.4% of intervention group and 56.1% of control group lost to follow‐up at 6‐month assessment. ITT analysis |