Acceptability and Utility of an Open-Access, Online Single-Session Intervention Platform for Adolescent Mental Health

Schleider, Jessica Lee; Dobias, Mallory; Sung, Jenna; Mumper, Emma; Mullarkey, Michael C

BACKGROUND: Many youths with mental health needs are unable to access care. Single-session interventions (SSIs) have helped reduce youth psychopathology across multiple trials, promising to broaden access to effective, low-intensity supports. Online, self-guided SSIs may be uniquely scalable, particularly if they are freely available for as-needed use. However, the acceptability of online SSI and their efficacy have remained unexamined outside of controlled trials, and their practical utility is poorly understood. OBJECTIVE: We evaluated the perceived acceptability and proximal effects of Project YES (Youth Empowerment & Support), an open-access platform offering three online SSIs for youth internalizing distress. METHODS: After selecting one of three SSIs to complete, participants (ages 11-17 years) reported pre- and post-SSI levels of clinically relevant outcomes that SSIs may target (eg, hopelessness, self-hate) and perceived SSI acceptability. User-pattern variables, demographics, and depressive symptoms were collected to characterize youths engaging with YES. RESULTS: From September 2019 through March 2020, 694 youths accessed YES, 539 began, and 187 completed a 30-minute, self-guided SSI. SSI completers reported clinically elevated depressive symptoms, on average, and were diverse on several dimensions (53.75% non-white; 78.10% female; 43.23% sexual minorities). Regardless of SSI selection, completers reported pre- to post-program reductions in hopelessness (d(av)=0.53; d(z)=0.71), self-hate (d(av)=0.32; d(z)=0.61), perceived control (d(av)=0.60; d(z)=0.72) and agency (d(av)=0.39; d(z)=0.50). Youths rated all SSIs as acceptable (eg, enjoyable, likely to help peers). CONCLUSIONS: Results support the perceived acceptability and utility of open-access, free-of-charge SSIs for youth experiencing internalizing distress. TRIAL REGISTRATION: Open Science Framework; osf.io/e52p3