Interest in Collaborative, Practice-Based Research Networks in Pediatric Refugee Health Care

Abstract

Over the last decade, approximately 200,000 refugee children have resettled across the United States. This population is dispersed, resulting in limited data. Collaborative research networks, where clinicians across distinct practice sites work together to answer research questions, can improve the evidence base regarding clinical care. We distributed a web-based survey to pediatric refugee providers around North America to assess priorities, perceived barriers and benefits to collaborative research. We recruited 57 participants. Of respondents, 89 % were interested in collaborative research, prioritizing: (1) access to health care (33 %), (2) mental health (24 %) and (3) nutrition/growth (24 %). Perceived benefits were “improving clinical practice” (98 %) and “raising awareness about the needs of pediatric refugees” (94 %). Perceived barriers were “too many other priorities” (89 %) and “lack of funding for data entry” (78 %). There is widespread interest in collaborative networks around pediatric refugee healthcare. A successful network will address barriers and emphasize priorities.

Appendices

Appendix 1

Feedback Requested: Caring for Refugee Children

Dear members,

We are interested in hearing about your experiences participating in the care of refugee children. We invite you to complete this 5 min long survey that will help inform the coordination of collaborative efforts to increase the quality of the care provided for refugee children.

By April 15th, please complete the online survey. If you would like follow up information, please include your name and email address at the end of the survey.

Please contact the study PI at [Study PI] for more information.

Thank you.

Study PI.

Appendix 2