Literature DB >> 31181137

Embedding research recruitment in a community resource e-prescribing system: lessons from an implementation study on Chicago's South Side.

Gillian Feldmeth1, Edward T Naureckas2, Julian Solway2, Stacy Tessler Lindau1,3.   

Abstract

OBJECTIVE: The study sought to implement and assess the CommunityRx e-prescribing system to recruit research participants from a predominantly non-Hispanic Black community on Chicago's South Side.
MATERIALS AND METHODS: CommunityRx integrates with electronic medical record systems to generate a personalized list of health-promoting community resources (HealtheRx). Between December 2015 and December 2016, HealtheRxs distributed at outpatient visits to adults with asthma or chronic obstructive pulmonary disease also incentivized participation in a pulmonary research registry. Usual practices for registry recruitment continued in parallel.
RESULTS: Focus groups established acceptability and appropriateness among the target population. Pulmonary research registry recruitment information was included on 13 437 HealtheRxs. Forty-one (90% non-Hispanic Black) patients responded with willingness to participate and 9 (8 non-Hispanic Black) returned a signed consent required to enroll. Usual recruitment practices enrolled 4 registrants (1 non-Hispanic Black). DISCUSSION: Automating research recruitment using a community e-prescribing system is feasible.
CONCLUSIONS: Implementation of an electronic medical record-integrated, community resource referral tool promotes enrollment of eligible underrepresented research participants; however, enrollment was low.
© The Author(s) 2019. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  electronic health records; health disparities; health information technology; minority health; patient recruitment

Year:  2019        PMID: 31181137      PMCID: PMC7587152          DOI: 10.1093/jamia/ocz059

Source DB:  PubMed          Journal:  J Am Med Inform Assoc        ISSN: 1067-5027            Impact factor:   4.497


  39 in total

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Review 3.  Effective recruitment and retention of minority research participants.

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Review 5.  Strategies addressing barriers to clinical trial enrollment of underrepresented populations: a systematic review.

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Authors:  Emily Pfaff; Adam Lee; Robert Bradford; Jinhee Pae; Clarence Potter; Paul Blue; Patricia Knoepp; Kristie Thompson; Christianne L Roumie; David Crenshaw; Remy Servis; Darren A DeWalt
Journal:  J Am Med Inform Assoc       Date:  2019-01-01       Impact factor: 4.497

7.  The use of electronic medical records for recruitment in clinical trials: findings from the Lifestyle Intervention for Treatment of Diabetes trial.

Authors:  Valery S Effoe; Jeffrey A Katula; Julienne K Kirk; Carolyn F Pedley; Linda Y Bollhalter; W Mark Brown; Margaret R Savoca; Stedman T Jones; Janet Baek; Alain G Bertoni
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Journal:  J Am Med Inform Assoc       Date:  2018-05-01       Impact factor: 4.497

Review 9.  Methods to increase response to postal and electronic questionnaires.

Authors:  Philip James Edwards; Ian Roberts; Mike J Clarke; Carolyn Diguiseppi; Reinhard Wentz; Irene Kwan; Rachel Cooper; Lambert M Felix; Sarah Pratap
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Journal:  JAMIA Open       Date:  2018-06-11
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  5 in total

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2.  Back to the Future: Achieving Health Equity Through Health Informatics and Digital Health.

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Review 3.  Human-Computer Interaction, Ethics, and Biomedical Informatics.

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4.  Promoting Inclusive Recruitment: a Qualitative Study of Black Adults' Decision to Participate in Genetic Research.

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Journal:  J Urban Health       Date:  2022-07-25       Impact factor: 5.801

Review 5.  Leveraging Electronic Health Records to Address Breast Cancer Disparities.

Authors:  Solange Bayard; Genevieve Fasano; Rulla M Tamimi; Pilyung Stephen Oh
Journal:  Curr Breast Cancer Rep       Date:  2022-09-03
  5 in total

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