Interactive Media-Based Approach for an Exception From Informed Consent Trial Involving Patients With Trauma

Author:

Stephens Shannon W.1,Carroll-Ledbetter Christy1,Duckert Sarah1,Coffman Tanner1,Nelson Margaret1,Brown Karen N.1,Rodgers Joel1,Griffin Russell L.1,Suen Amy2,Casey Jeremy2,Sloan Steven R.2,Goldstein Brahm2,McClintock Adam Joseph3,Goldkind Sara F.4,Gelinas Luke5,Higley Amanda E.5,Joseph Bellal A.6,Holcomb John B.1,Jansen Jan O.1, ,Afaneh Amer A.7,Agarwal Suresh7,Anand Tanya7,Anderson Jeffrey H.7,Arbabi Saman7,Ashley Dennis W.7,Bardes James7,Benjamin Elizabeth R.7,Bjordahl Paul M.7,Bochicchio Grant V.7,Bugaev Nikolay7,Butts Charles C7,Cannon Jeremy W.7,Carlin Margo7,Claridge Jeffrey A7,Coimbra Raul7,Cox Daniel B7,Cross Alisa7,Dorlac Warren C7,Driver Brian E.7,Dubose Joseph7,Gandhi Raj R.7,George Richard7,Goodman Michael D.7,Hoth Jason7,Hu Charles7,Iyegha Uroghupatei P.7,Jacobson Lewis E.7,Jenkins Donald H.7,Kalkwarf Kyle J.7,Kepros John P.7,Kutcher Matthew E.7,Leeper Christine M.7,Lueckel Stephanie N.7,Machado-Aranda David A.7,Majercik Sarah D.7,Maung Adrian A.7,McKenzie Katherine E.7,Meizoso Jonathan P.7,Nahmias Jeffry7,O'Keeffe Terence7,Rojavin Yuri7,Ross Samuel W7,Samra Navdeep S.7,Schreiber Martin7,Schroeppel Thomas J7,Stevens Timothy J.7,Weinberg Jordan A.7,Wertin Thomas M7,Wilson Chad T.7,Wisler Jonathan7,Zreik Khaled7

Affiliation:

1. Center for Injury Science, University of Alabama at Birmingham, Birmingham

2. Hematology Therapeutic Research Area, CSL Behring, King of Prussia, Pennsylvania

3. Office of Institutional Review Board, University of Alabama at Birmingham, Birmingham

4. Goldkind Consulting LLC, Potomac, Maryland

5. Advarra, Columbia, Maryland

6. Department of Surgery, University of Arizona, Tucson

7. for the TAP Study Group

Abstract

ImportanceException From Informed Consent (EFIC) research requires community consultation (CC) and public disclosure (PD). Traditional methods of conducting CC and PD are slow, expensive, and labor intensive.ObjectiveTo describe the feasibility and reach of a novel interactive, media-based approach to CC and PD and to identify the similarities and differences between trial sites in website views, survey responses, online community forum attendance, and opt-out requests.Design, Setting, and ParticipantsThis survey study analyzed the CC and PD campaigns conducted for the TAP trial (Evaluation of BE1116 in Patients With Traumatic Injury and Acute Major Bleeding to Improve Survival), an EFIC trial of the early administration of prothrombin complex concentrate in patients with trauma. The CC and PD campaigns consisted of social media advertisements, linked websites, community surveys, and online community forums. These activities were coordinated from a central site and approved by a central institutional review board. This study focused on the first 52 of 91 TAP trial sites (level I trauma centers) in the US to have completed their CC and PD campaigns. Community members in the catchment areas of the participating trauma centers were targeted. Data analysis was conducted between October 2023 and February 2024.ExposureSocial media advertisements, surveys, and online community meetings conducted as part of the CC and PD campaign for the TAP trial.Main Outcomes and MeasuresSocial media campaign reach and engagement, web page views, survey results, online community forum attendance, and opt-out requests.ResultsFifty-two trial sites were approved for participant enrollment. Social media advertisements were displayed 92 million times, reaching 11.8 million individuals. The median (IQR) number of people reached in each location was 210 317 (172 068-276 968). Site-specific websites were viewed 144 197 times (median [IQR] viewings per site, 2984 [1267-4038]). A total of 17 206 fully or partly completed surveys were received, and survey respondents had a median (IQR) age of 40.1 (15-65) years and included 10 444 females (60.7%). Overall, 60.6% survey respondents said they would want to be entered into the trial even if they could not give consent, 87.7% agreed that emergency care research was necessary, and 88.0% agreed that the TAP trial should be conducted in their community. Online community forums were attended by a median (IQR) number of 38 (20-63) people. Four opt-out requests were received.Conclusions and RelevanceThe interactive media-based approach to CC and PD for the ongoing TAP trial showed the feasibility and benefits of executing an efficient, coordinated, centrally run series of locally branded and geographically targeted CC and PD campaigns for a large EFIC study.

Publisher

American Medical Association (AMA)

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