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A brief digital screening tool to address parental and adolescent tobacco and electronic cigarette use in paediatric medical care in Canada: a pilot randomized controlled trial

Olivier Drouin, Tamara Perez, Émile Diamant, Cristal Namuhoranye, Sandrine Mitri, Afnan Al-Saleh, M. Sylvestre, Jennifer O'Loughlin et al.

Pilot and Feasibility Studies, 2026

53 participants · 2 citations

Abstract

Background Tobacco use is a strong risk factor for premature mortality and morbidity. We assessed the feasibility of screening and recruiting participants for a randomized controlled trial (RCT) of a facilitated referral intervention to promote smoking and vaping cessation among parents and children (CanCEASE). Methods We conducted a pilot RCT of CanCEASE in five outpatient pediatric clinics in Montreal, Canada. We recruited parents (≥ 18 years) and adolescents (14–17 years) who reported smoking or vaping in the 7 days prior to recruitment. Our primary outcome was the number of participants recruited and randomized per day of recruitment (> 0.6/day). Secondary outcomes included interest in cessation resources (binary, at least one resource requested by the end of participation at 6 months) and participant retention (≥ 60% at 6 months). Descriptive statistics are presented, and outcomes are compared between parent and adolescent participants using chi-square tests. Results There were 118 days of recruitment across 5 clinics spread over 95 calendar days, resulting in enrollment of 53 adolescents and 74 parents in the study, with the majority being female. Recruitment rates were 0.56 participant/day of recruitment for adolescents and 0.78 participant/day of recruitment for parents. Interest in specific cessation resources was low overall. Retention rate at 6 months was 52.8% (95% confidence interval: 43.7–61.6) and higher among adolescents (vs. parents) and females (vs. males).…

How strong is the evidence?

Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 53 participants or records.

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