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. Author manuscript; available in PMC: 2014 Feb 2.
Published in final edited form as: Genet Med. 2013 Sep 12;15(10):792–801. doi: 10.1038/gim.2013.127

Table 2.

Patient engagement strategies by implementation phase

Selection phase Preimplementation phase Implementation phase Postimplementation phase
Sample topics
  • What are patients’ attitudes toward genomic medicine?

  • What are patients’ concerns about privacy, security, discrimination, or insurance coverage with regard to genomic data?

  • What are patients’ expectations regarding access—theirs and others’— to their genomic data?

  • What do patients think about the possibility of learning about the range of results that can be generated through sequencing?

  • Which information should be provided directly to patients via Web portal or other EMR-linked tools?

  • What kinds of online resources should be made available to patients?

  • What kinds of report formats are appropriate for patient use?

  • What kinds of printable patient education materials might be needed within the EMR?

  • What should the informed consent process look like?

  • How can we optimize patient engagement around genomic information?

  • How do patients respond to the inclusion of genomic information during the clinic visit?

  • Do patients want more information? Less?

  • Are additional patient education materials needed?

  • Are patients aware that the innovation has been launched?

  • Does providing genomic information to patients increase satisfaction with care?

  • Does the integration of genomics into routine care affect relevant health behaviors?

  • Does the implementation of genomic medicine increase satisfaction with the patient’s health plan?

Sample methods
  • Informational articles in newsletters and on websites

  • In-clinic information: e.g., posters, brochures, kiosks

  • Community conversations or town hall meetings

  • Focus groups

  • Interviews

  • Advisory boards

  • Surveys (online, telephone)

  • Focus groups

  • Usability testing

  • Community leaders

  • Participatory design of patient education and consent materials

  • Launch communications: e.g., promotional materials, announcements, posters, giveaways

  • Postvisit surveys

  • Brief in-clinic interviews

  • Focus groups

  • Periodic satisfaction surveys

  • Focus groups

  • One-to-one interviews

  • Feedback reports and updates via existing communication vehicles

Implementation stages drawn from Lorenzi et al.;19 remainder, authors’ analysis.

EMR, electronic medical record.