@article{c739930ce41c40eb814372abd2b18b8a,
title = "Recruitment of trial participants through electronic medical record patient portal messaging: A pilot study",
abstract = "Background/aim: Cost-efficient methods are essential for successful participant recruitment in clinical trials. Patient portal messages are an emerging means of recruiting potentially eligible patients into trials. We assessed the response rate and complaint rate from direct-to-patient, targeted recruitment through patient portals of an electronic medical record for a clinical trial, and compared response rates by differences in message content. Methods: The Study to Understand Fall Reduction and Vitamin D in You (STURDY) trial is a National Institutes of Health–sponsored, community-based study of vitamin D supplementation for fall prevention in older adults conducted at Johns Hopkins. Potential participants were identified using the Epic electronic medical record at the Johns Hopkins Health System based on age (≥70 years), ZIP code (30-mile radius of study site), and prior activation of a patient portal account. We prepared a shorter message and a longer message. Both had basic information about study participation, but the longer message also contained information about the significance of the study and a personal invitation from the STURDY principal investigator. The Hopkins Institutional Review Board did not require prior consent from the patient or their providers. We calculated the response rate and tracked the number of complaints and requests for removal from future messages. We also determined response rate according to message content. Results: Of the 5.5 million individuals receiving care at the Johns Hopkins Health System, a sample of 6896 met our inclusion criteria and were sent one patient portal recruitment message between 6 April 2017 and 3 August 2017. Assessment of enrollment by this method ended on 1 December 2017. There were 116 patients who expressed interest in the study (response rate: 1.7%). Twelve (0.2%) recipients were randomized. There were two complaints (0.03%) and one request to unsubscribe from future recruitment messages (0.01%). Response rate was higher with the longer message than the shorter message (2.1% vs 1.2%; p = 0.005). Conclusion: Patient portal messages inviting seniors to participate in a randomized controlled trial resulted in a response rate similar to commercial email marketing and resulted in very few complaints or opt-out requests. Furthermore, a longer message with more content enhanced response rate. Recruitment through patient portals might be an effective strategy to enroll trial participants.",
keywords = "Clinical trial, electronic medical records, patient portal messages, randomized controlled trial, recruitment methods",
author = "{for the STURDY Collaborative Research Group} and Plante, {Timothy B.} and Gleason, {Kelly T.} and Miller, {Hailey N.} and Jeanne Charleston and Kristen McArthur and Himmelfarb, {Cheryl Dennison} and Mariana Lazo and Ford, {Daniel E.} and Miller, {Edgar R.} and Appel, {Lawrence J.} and Juraschek, {Stephen P.} and Nicole Cronin and Scott McClure and Jennifer Miskimon and Mitchell, {Christine M.} and Kalyani, {Rita R.} and Roth, {David L.} and Schrack, {Jennifer A.} and Szanton, {Sarah L.} and Jacek Urbanek and Jeremy Walston and Amal Wanigatunga and Baksh, {Sheriza N.} and Blackford, {Amanda L.} and Shumon Chattopadhyay and Drye, {Lea T.} and John Dodge and Cathleen Ewing and Sana Haider and Holland, {Stephanie C.} and Rosetta Jackson and Andrea Lears and Curtis Meinert and David Shade and Michael Smith and Sternberg, {Alice L.} and James Tonascia and {Van Natta}, {Mark L.} and Annette Wagoner and Comstock, {George W.} and Michos, {Erin D.} and Bennett, {J. Denise} and Pamela Bowers and Josef Coresh and Patricia Crowley and Tammy Crunkleton and Briana Dick and Rebecca Evans and Mary Godwin and Lynne Hammann",
note = "Funding Information: The authors thank the participants and the field center staff for their invaluable contributions to the STURDY trial. The authors thank National Institutes of Health and its Institutes for supporting multiple aspects of this work. STURDY is supported by the National Institute on Aging (U01AG047837). The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by the National Institute on Aging (5U01AG047837-04). Research reported in this publication was supported by the National Institute on Aging of the National Institutes of Health (NIH/NIA) under Award Number U01AG047837. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The Office of Dietary Supplements (ODS) also supported this research. T.B.P. was sponsored by grants from Health Resources and Services Administration (T32HP10025B0) and National Heart, Lung, and Blood Institute (NHLBI, 2T32HL007180-41A1). S.P.J. was supported by National Institute of Diabetes and Digestive and Kidney Diseases (T32DK007732) and the NHLBI (K23HL135273). K.T.G. and H.N.M. were supported by a predoctoral fellowship in Interdisciplinary Training in Cardiovascular Health Research (T32NR012704). K.T.G. was also supported by a Predoctoral Clinical Research Training Program (TL1TR001078). M.L. was supported by grants from the National Institute of Diabetes and Digestive and Kidney Diseases (R01DK089174, R01DK108784, and U01DK061730), National Heart, Lung, and Blood Institute (UH3HL130688-02), and National Institute of Alcohol Abuse and Alcoholism (U10AA025286). Funding Information: Patient portal messages inviting seniors to participate in a randomized controlled trial resulted in a response rate similar to commercial email marketing and resulted in very few complaints or opt-out requests. Furthermore, a longer message with more content enhanced response rate. Recruitment through patient portals might be an effective strategy to enroll trial participants. Clinical trial randomized controlled trial recruitment methods electronic medical records patient portal messages National Institute on Aging https://doi.org/10.13039/100000049 5U01AG047837-04 National Center for Advancing Translational Sciences https://doi.org/10.13039/100006108 UL1TR001079 edited-state corrected-proof The authors thank the participants and the field center staff for their invaluable contributions to the STURDY trial. The authors thank National Institutes of Health and its Institutes for supporting multiple aspects of this work. STURDY is supported by the National Institute on Aging (U01AG047837). Members of the STURDY Collaborative Research Group by center: At Johns Hopkins University Centers: Welch Center for Prevention, Epidemiology and Clinical Research: Lawrence J. Appel, MD, MPH (chair); Nicole Cronin; Stephen P. Juraschek, MD, PhD; Scott McClure, MS; Jennifer Miskimon; Christine M. Mitchell, ScM; Timothy B. Plante, MD, MHS. Center on Aging and Health: Rita R. Kalyani, MD, MHS; David L. Roth, PhD; Jennifer A. Schrack, PhD; Sarah L. Szanton, PhD; Jacek Urbanek, PhD; Jeremy Walston, MD; Amal Wanigatunga, PhD. STURDY Data Coordinating Center: Sheriza N. Baksh, PhD; Amanda L. Blackford, ScM; Shumon Chattopadhyay, MSE; Lea T. Drye, PhD; John Dodge; Cathleen Ewing; Sana Haider, BS; Stephanie C. Holland, BS; Rosetta Jackson; Andrea Lears, BS; Curtis Meinert, PhD; David Shade, JD; Michael Smith, BS; Alice L. Sternberg, ScM; James Tonascia, PhD; Mark L. Van Natta, MHS; Annette Wagoner. Clinical Field Centers, Johns Hopkins University: George W. Comstock Center for Public Health Research and Prevention: Erin D. Michos, MD, MHS (Site PI); J. Denise Bennett; Pamela Bowers; Josef Coresh, MD, PhD; Patricia Crowley, MS; Tammy Crunkleton; Briana Dick, BA; Rebecca Evans, RN; Mary Godwin; Lynne Hammann; Deborah Hawks; Karen Horning; Erika Hull; Brandi Mills; Melissa Minotti, MPH; Leann Raley; Amanda Reed, MS; Rhonda Reeder, RN; Cassie Reid; Melissa Shuda; Adria Spikes; Rhonda Stouffer; Kelly Weicht. ProHealth Clinical Research Unit: Edgar R. Miller III, MD, PhD (Site PI); Caroline Abbas; Bernellyn Carey, BS; Jeanne Charleston, BSN, RN; Syree Davis, BS; Naomi DeRoche-Brown; Debra Gayles, BS; Sherlina Holland; Ina Glenn-Smith; Duane Johnson; Mia Johnson; Eva Keyes; Kristen McArthur; Danielle Santiago; Chanchai Sapun; Valerie Sneed; Lee Swartz, MBA; Letitia Thomas. At the University of Maryland School of Medicine Laboratory: Robert H. Christenson, PhD; Show-Hong Duh, PhD; Heather Rebuck. At the Data and Safety Monitoring Board (DSMB): Clifford Rosen, MD (chair, Maine Medical Center Research Institute); Tom Cook, PhD (University of Wisconsin); Pamela Duncan, PhD (Wake Forest Baptist Health); Karen Hansen, MD, MS (2016-2019, University of Wisconsin); Anne Kenny, MD (2014-2016, University of Connecticut); Sue Shapses, PhD, RD (Rutgers University). At the National Institute on Aging (NIA): Judy Hannah, PhD; Sergei Romashkan, MD. At the Office of Dietary Supplements (ODS): Cindy D. Davis, PhD; Christopher T. Sempos, PhD. Consultants: Jack M. Guralnik, MD, PhD (University of Maryland School of Medicine); J.C. Gallagher, MD (Creighton University School of Medicine). Declaration of conflicting interests The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. Funding The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by the National Institute on Aging (5U01AG047837-04). Research reported in this publication was supported by the National Institute on Aging of the National Institutes of Health (NIH/NIA) under Award Number U01AG047837. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The Office of Dietary Supplements (ODS) also supported this research. T.B.P. was sponsored by grants from Health Resources and Services Administration (T32HP10025B0) and National Heart, Lung, and Blood Institute (NHLBI, 2T32HL007180-41A1). S.P.J. was supported by National Institute of Diabetes and Digestive and Kidney Diseases (T32DK007732) and the NHLBI (K23HL135273). K.T.G. and H.N.M. were supported by a predoctoral fellowship in Interdisciplinary Training in Cardiovascular Health Research (T32NR012704). K.T.G. was also supported by a Predoctoral Clinical Research Training Program (TL1TR001078). M.L. was supported by grants from the National Institute of Diabetes and Digestive and Kidney Diseases (R01DK089174, R01DK108784, and U01DK061730), National Heart, Lung, and Blood Institute (UH3HL130688-02), and National Institute of Alcohol Abuse and Alcoholism (U10AA025286). Trial registration ClinicalTrials.gov: NCT02166333. ORCID iD Timothy B Plante https://orcid.org/0000-0001-9992-9597 Supplemental material Supplemental material for this article is available online. Publisher Copyright: {\textcopyright} The Author(s) 2019.",
year = "2020",
month = feb,
day = "1",
doi = "10.1177/1740774519873657",
language = "English (US)",
volume = "17",
pages = "30--38",
journal = "Clinical Trials",
issn = "1740-7745",
publisher = "SAGE Publications Ltd",
number = "1",
}