The Impact Integrated Data System for Quality and Outcomes Tracking of Prevention Programs
Completed · Not applicable
Conditions studied: Trauma, Psychological, Social Skills, Family Dysfunctional
In brief
There has been substantial progress in developing evidence-based prevention programs (EBPPs) for preventing risky behaviors and promoting positive outcomes for youth. Unfortunately, their adoption, quality implementation, long-term sustainability, and scalability in real world service settings, continues to lag far behind resulting in an inability to achieve the intended broad scale public impact. This SBIR Phase II project will build on the findings and feedback gathered from stakeholders in the Phase I project to fully develop and test the Impact implementation support system. Impact will provide an easy to use, cost- and time-efficient technology platform that is capable of (a) gathering relevant process and outcomes data in a feasible way within real-world service settings; (b) producing real-time analytics (e.g., graphical displays) and meaningful reports at the provider, service setting, and broader levels (e.g., state-wide); and (c) linking data analytics to continuous quality improvement (CQI) feedback to help providers achieve best practices and targeted youth outcomes.
Key facts
- Study ID
- NCT03622138
- Run by
- 3-C Institute for Social Development
- People needed
- 203
- Starts
- 2018-06-08
- Expected to finish
- 2021-07-31
- Last updated by the study team
- 2022-07-12
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Must be an Evidence-based Prevention Program Provider
- Regularly implement one of the three supported EBPPs to youth in a school or community setting
- Commit to implementing that EBPP over the study period (approximately one school year)
- Serve a minimum of 10 youth over the study period
- Be willing to allow 3C researchers to collect data from their setting
Where it is running
- 3C Institute — Durham, North Carolina, United States
Full record on ClinicalTrials.gov
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