The objective of this study was to compare the effects of using electronic health records (EHRs) equipped with insurance enrollment tracking forms versus using nonautomated and nonstandardized tracking outside of EHRs on pediatric patients’ health insurance status, healthcare utilization, and receipt of recommended pediatric care in community health centers (CHCs).

Project page: Using Electronic Health Records at Community Health Centers to Help Children Get Health Insurance and Access Health Care
Principal Investigator: Jennifer E. DeVoe, MD, DPhil
Organization: Oregon Community Health Information Network
Original project title: Innovative Methods for Parents and Clinics to Create Tools (IMPACCT) for Kids’ Care
HSRProj ID: 20142235
ClinicalTrials.gov ID: NCT02298361

To cite this document, please use: DeVoe J, Rachel Gold R, Nelson C., et al. 2018. Using Electronic Health Records at Community Health Centers to Help Children Get Health Insurance and Access Health Care. Washington, DC: Patient‐Centered Outcomes Research Institute (PCORI). https://doi.org/10.25302/6.2018.CER.308  

Tags

What's Happening at PCORI?

The Patient-Centered Outcomes Research Institute sends weekly emails about opportunities to apply for funding, newly funded research studies and engagement projects, results of our funded research, webinars, and other new information posted on our site.

Subscribe to PCORI Emails

Image

Hand pointing to email icon