Study protocol testing toolkit versus usual care for implementation of screening, brief intervention, referral to treatment in hospitals: a phased cluster randomized approach

dc.contributor.authorNewhouse, Robin
dc.contributor.authorJanney, Michelle
dc.contributor.authorGilbert, Anne
dc.contributor.authorAgley, Jon
dc.contributor.authorBakoyannis, Giorgos
dc.contributor.authorFerren, Melora
dc.contributor.authorMullins, C. Daniel
dc.contributor.authorJohantgen, Meg
dc.contributor.authorSchwindt, Rhonda
dc.contributor.authorThoele, Kelli
dc.contributor.departmentSchool of Nursingen_US
dc.date.accessioned2019-07-03T17:25:07Z
dc.date.available2019-07-03T17:25:07Z
dc.date.issued2018-12-27
dc.description.abstractBACKGROUND: Alarming rates of unhealthy alcohol, non-prescription drug, and tobacco use highlight the preventable health risks of substance abuse and the urgent need to activate clinicians to recognize and treat risky use. Screening, brief intervention, and referral to treatment (SBIRT) is an efficacious and effective processes to identify, reduce and prevent risky use of substances. This paper describes a study protocol testing implementation of a toolkit to enhance use of SBIRT in acute care settings to recognize and address patient risky alcohol, drug, and tobacco use. METHODS: This study uses a phased cluster randomized mixed method design to test nurse-led implementation of an SBIRT toolkit on one medical-surgical unit at 14 acute care hospitals (critical access, community and academic health centers). Medical surgical units will be randomly assigned to implement the SBIRT toolkit (engagement and communication, assessment, planning, training, and evaluation tools) or a wait-list usual care control group that begins implementation 6 months later. Primary endpoints are documentation of SBIRT delivery in randomly selected electronic medical records at baseline, 6 months and 12 months after group 1 implementation (61 records per unit per time period, N = 2562). Two surveys will be administered to unit nurses: smoking cessation activities will be assessed at baseline and SBIRT use will be assessed on randomly-selected days after implementation. In addition, site coordinators will complete a baseline capacity assessment, an implementation fidelity survey post-implementation, and a structured interview at the end of the study. Multilevel mixed-effects effects logistic and linear models will be used to analyze use of SBIRT and cost outcomes. DISCUSSION: This study will guide subsequent SBIRT implementation, dissemination, and spread across rural, community and urban healthcare systems throughout the state and beyond. The long-term objective is to activate clinicians to recognize, intervene and refer people with risky substance use to improve health and decrease substance use disorders. Trial registration ClinicalTrials.goven_US
dc.identifier.citationNewhouse, R., Janney, M., Gilbert, A., Agley, J., Bakoyannis, G., Ferren, M., … Thoele, K. (2018). Study protocol testing toolkit versus usual care for implementation of screening, brief intervention, referral to treatment in hospitals: a phased cluster randomized approach. Addiction science & clinical practice, 13(1), 28. doi:10.1186/s13722-018-0130-4en_US
dc.identifier.urihttps://hdl.handle.net/1805/19829
dc.language.isoen_USen_US
dc.publisherBiomed Centralen_US
dc.relation.isversionof10.1186/s13722-018-0130-4en_US
dc.relation.journalAddiction Science & Clinical Practiceen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.sourcePMCen_US
dc.subjectAcute careen_US
dc.subjectAlcoholen_US
dc.subjectImplementationen_US
dc.subjectNurseen_US
dc.subjectSBIRTen_US
dc.subjectSubstance useen_US
dc.subjectTobaccoen_US
dc.subjectToolkiten_US
dc.titleStudy protocol testing toolkit versus usual care for implementation of screening, brief intervention, referral to treatment in hospitals: a phased cluster randomized approachen_US
dc.typeArticleen_US
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