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Research Permissions Management System (RPMS )

Research Permissions Management System (RPMS ). Jihad Obeid, MD Acting Director, Biomedical Informatics Center  Health Sciences South Carolina South Carolina Clinical and Translational Research Institute Medical University of South Carolina

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Research Permissions Management System (RPMS )

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  1. Research Permissions Management System (RPMS) Jihad Obeid, MD Acting Director, Biomedical Informatics Center  Health Sciences South Carolina South Carolina Clinical and Translational Research Institute Medical University of South Carolina GO GRANT (National Lib of Med Grant # 1RC2 LM010796)

  2. Research Permissions Management System (RPMS): The Case For Change Current Environment New Permissions Management • Electronic recording of consents and permissions • Access to permission decisions for research • Common permissions terminology • Facilitating research while enhancing compliance with patient wishes • Rich educational opportunities about the research process • Patients will have easy access to their permission decisions (patient portal) • Tracking of informed consent versions • Paper-basedconsents and permissions • Permissions data are unavailable for analysis • The number of patients who are generally favorable to research participation is unknown • Inconsistent process and semanticsin obtaining permissions across multiple hospitals • Poor comprehension and satisfaction in subjects providing permission • Research volunteer subject lists are localized

  3. A Research Permission Management SystemGO grant Concept

  4. Permission as a Searchable Attribute in i2b2 Show me how many males with Diabetes over 65 have given permission to be contacted for research Other permissions include participation in: Biobank or Disease Registries, etc.

  5. Collaborative Project – Distinct trackswith several partners: • Discovery Phase (USC, MUSC, Clemson) • Creation of the RPMS application initiated with SAIC and Recombinant – later brought in-house • Duke Ethics/Legal/Social (ELSI) Process and creation of the General Research Permissions Form • Clemson Permissions research project and human subjects “Permissions UI Laboratory” Duke ELSI Clemson Discovery & UI Lab MUSC Informatics Oversight & Software Development Design of the end-to-end RPMS application for Pilot

  6. Phased project • RPMS version 1 (+ end-to-end pilot) • RPMS version 2 (added features, open source release)

  7. RPMS Pilot Program • Workflow analyzed at HSSC members (PH, Greenville, MUSC) + All solicited to participate in Pilot. • Select patient registration clinics at MUSC (timing was right) • Pilot Nov 2011 – Nov 2012. • Clerk Training& Feedback. • Over 2500 patients have been registered using the RPMS pilot at MUSC. • Adopted at University of Florida (for informed consent)

  8. RPMS Pilot Architecture CDW EMPI (f) (c) (d) (b) EMR (e) (a)

  9. RPMS Pilot well received

  10. RPMS version 2: KEY FEATURES • Includes RPMS Pilot functionality for patient registration • Add Informed Consent and HIPAA Authorizations • Design: Configurable, Extensible, Easy to Use • Includes Authoring Module/Form Designer for broad tool applicability • Ability to embed Rich Media content into forms (e.g. video) • Robust Architecture: Plug-in style and Ontology-based (graph database at its core) • Nodes and relationships are flexible, extensible • Handles large and complex datasets (scalable) • Indexes to transverse relationships (performance) • Published as Open Source product (Compared to custom developed application)

  11. RPMS Demo • Typical Informed Consent for Research Workflow: • Research coordinator login • Collecting a consent from the patient • Document review and witness signature

  12. Research coordinator login

  13. Research coordinator selects clinic (multi-clinic/multi-protocol)

  14. Research coordinator selects Research Participant

  15. If a registered patient – system will find Encounter ID

  16. Research coordinator selects research Protocol & Language Then hands off to Participant

  17. Participant goes through consent

  18. Participant selects research permissions and signs consent

  19. Participant completes consent then hands back to Research Coordinator

  20. The system locks patient out for security Research Coordinator has to enter the unlock code.

  21. Research Coordinator reviews consent with Participant

  22. Witness signature

  23. Now ready for next participant End of Demo

  24. Released as open source http://www.healthsciencessc.org/rpms/

  25. Publications/Presentations 1. Obeid J, Gabriel D, Sanderson I, editors. A biomedical research permissions ontology: cognitive and knowledge representation considerations. 26th Annual Computer Security Applications Conference, Governance of Technology, Information and Policies; 2010 Dec 2010; Austin, TX: ACM New York, NY, USA. 2. ChalilMadathil K, Koikkara R, Gramopadhye AK, Fryar K, editors. An Analysis of the General Consenting Process in an Emergency Department at a Major Hospital: Challenges for Migrating to an Electronic Health Record. Proceedings of the 2011 Industrial Engineering Research Conference; 2011; Reno, NV. • Alexander R, Obeid J, Sanderson I. Piloting a Research Permissions Management System on a portable Device. Proceedings of the 2012 Summit on Clinical Research Informatics. San Francisco, CA: The American Medical Informatics Association; 2012. • Obeid JS, Gerken K, Chalil KM, Rugg D, Alstad CE, Fryar K, et al. Development of an Electronic Research Permissions Management System to Enhance Informed Consents and Capture Research Authorizations Data. Proceedings of the 2013 Summit on Clinical Research Informatics. 2013 PENDING JOURNAL SUBMISIONS: 4. ChalilMadathil K, Koikkara R, Obeid JS, Greenstein JS, Sanderson IC, Fryar K, et al. Findings from the Research Studies Conducted during the Design and Development of a State-Wide Electronic Consenting System. International Journal of Medical Informatics. 2012:Submitted. 5. Sanderson IC, Obeid JS, Chalil KM, Gerken K, Fryar K, Rugg D, et al. Managing Clinical Research Permissions Electronically: a Novel Approach to Enhancing Recruitment and Managing Consents. Clinical Trials. 2012:Submitted.

  26. Opportunities • HSSC Institutions expressed interest: Spartanburg, Hollings Cancer Center • Collaborations: • University of Florida, Clemson. • NCI FOA: U24 • Commercialization: • Discovery Disclosures • Exploring business models (Rich content-Player/Distribution) • College of Charleston

  27. Acknowledgements RPMS core team Iain Sanderson, MSc, FRCA Katrina Fryar Randall Alexander Rick Larsen Dan Rugg Katie Gerken Jay Moskowitz, PhD (PI) Clemson University AnandGramopadhye, PhD KapilMadathil • Funded by NIH/NLM Grant 1RC2LM010796-01 (09/30/2009 – 09/29/2012) • An Open Source Research Permissions Framework for South Carolina • And by NCRR/ CTSA Grant 1UL1RR029882-01 (7/14/09-03/31/14) • South Carolina Clinical & Translational Research Institute (SCTR) • And by

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