CompletedNot Applicable

Michigan Youth Violence Prevention Center: Building Evidence for Gun Violence Prevention - SafERteens Implementation

United States171 participantsStarted 2023-02-28

Plain-language summary

The purpose of this study is to determine the preliminary efficacy (via a micro-randomized trial \[MRT\] design) of augmenting Enhanced-Replicating Effective Program (E-REP) with engagement strategies to increase and sustain reach by healthcare providers (e.g., nurses, social workers) during implementation of the SafERteens program across multiple healthcare settings.

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: * Employed at study site * Participate in screening and/or SafERteens delivery. Exclusion Criteria: * Would not be expected to complete screening and/or intervention delivery * Would not begin screening and/or delivering SafERteens within the first 9 months of cohort implementation

What they're measuring

Preliminary Efficacy: weekly reach by providers

Timeframe: From the start of implementation to 52 weeks or the end of provider's employment if before 52 weeks.

Preliminary Efficacy: monthly reach by providers

Timeframe: From the start of implementation to 52 weeks or the end of provider's employment if before 52 weeks.

Trial details

NCT IDNCT05821205

SponsorUniversity of Michigan

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-04-13

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