CONTEXT: Recent federal regulations allow for emergency research without prospective consent provided that additional protections for the subjects are provided. One of these is community consultation. OBJECTIVE: To determine how to feasibly consult the community and what to do with the findings. DESIGN, SETTING, AND PARTICIPANTS: In connection with an ongoing study of l-arginine for brain injury at a public hospital's trauma center, we consulted three sets of community representatives using different methods. To sample the entire population of the county, we conducted a random-digit dialing survey (456 residents). To sample individuals served by the hospital, we interviewed a convenience sample of 566 patients and individuals in the waiting area. To sample particularly interested individuals, we conducted a series of public meetings (114 participants). In each case, the same instrument was used to ascertain their attitudes toward the study in general and toward its major features (randomization, waiver of consent, location, risks/benefits). To control for framing effects, items were randomly presented in a positive or negative fashion. RESULTS: All methods proved feasible, but telephone surveys were most efficient and guaranteed the desired demography. Even for a very low-risk study, only 79.75% of respondents would be willing to participate. The rate of approval for the major features was lower, with only 67.78% approving of the risk/benefit ratio, 53.7% approving of randomization, 57.66% approving of the consent waiver, and 44.45% approving of the location. The most significant factors affecting the rate of approval were the method of consultation and the framing of items (both p < .001), age, ethnicity, and previous research participation (all p < .01). CONCLUSIONS: Community consultation is feasible, but its results depend heavily on method of consultation, framing of questions, and choice of community. It may well demonstrate unexpectedly substantial opposition. There needs to be a better definition of the process and a better understanding of how to respond to its results.
CONTEXT: Recent federal regulations allow for emergency research without prospective consent provided that additional protections for the subjects are provided. One of these is community consultation. OBJECTIVE: To determine how to feasibly consult the community and what to do with the findings. DESIGN, SETTING, AND PARTICIPANTS: In connection with an ongoing study of l-arginine for brain injury at a public hospital's trauma center, we consulted three sets of community representatives using different methods. To sample the entire population of the county, we conducted a random-digit dialing survey (456 residents). To sample individuals served by the hospital, we interviewed a convenience sample of 566 patients and individuals in the waiting area. To sample particularly interested individuals, we conducted a series of public meetings (114 participants). In each case, the same instrument was used to ascertain their attitudes toward the study in general and toward its major features (randomization, waiver of consent, location, risks/benefits). To control for framing effects, items were randomly presented in a positive or negative fashion. RESULTS: All methods proved feasible, but telephone surveys were most efficient and guaranteed the desired demography. Even for a very low-risk study, only 79.75% of respondents would be willing to participate. The rate of approval for the major features was lower, with only 67.78% approving of the risk/benefit ratio, 53.7% approving of randomization, 57.66% approving of the consent waiver, and 44.45% approving of the location. The most significant factors affecting the rate of approval were the method of consultation and the framing of items (both p < .001), age, ethnicity, and previous research participation (all p < .01). CONCLUSIONS: Community consultation is feasible, but its results depend heavily on method of consultation, framing of questions, and choice of community. It may well demonstrate unexpectedly substantial opposition. There needs to be a better definition of the process and a better understanding of how to respond to its results.
Authors: Joni R Beshansky; Patricia R Sheehan; Kenneth J Klima; Nira Hadar; Ellen M Vickery; Harry P Selker Journal: Clin Trials Date: 2014-04 Impact factor: 2.486
Authors: Jose-Miguel Yamal; Claudia S Robertson; M Laura Rubin; Julia S Benoit; H Julia Hannay; Barbara C Tilley Journal: Clin Trials Date: 2014-04 Impact factor: 2.486
Authors: Neal W Dickert; Prasanthi Govindarajan; Deneil Harney; Robert Silbergleit; Jeremy Sugarman; Kevin P Weinfurt; Rebecca D Pentz Journal: Prehosp Emerg Care Date: 2014-01-08 Impact factor: 3.077
Authors: C E Hall; M Mirski; Y Y Palesch; M N Diringer; A I Qureshi; C S Robertson; R Geocadin; C A C Wijman; P D Le Roux; Jose I Suarez Journal: Neurocrit Care Date: 2012-02 Impact factor: 3.210
Authors: Carrie A Sims; Joshua A Isserman; Daniel Holena; Latha Mary Sundaram; Nikolai Tolstoy; Sarah Greer; Seema Sonnad; Jose Pascual; Patrick Reilly Journal: J Trauma Acute Care Surg Date: 2013-01 Impact factor: 3.313
Authors: Neal W Dickert; Victoria M Scicluna; Jill M Baren; Michelle H Biros; Ross J Fleischman; Prasanthi R Govindarajan; Elizabeth B Jones; Arthur M Pancioli; David W Wright; Rebecca D Pentz Journal: Crit Care Med Date: 2015-03 Impact factor: 7.598
Authors: Neal W Dickert; Victoria A Mah; Jill M Baren; Michelle H Biros; Prasanthi Govindarajan; Arthur Pancioli; Robert Silbergleit; David W Wright; Rebecca D Pentz Journal: Resuscitation Date: 2013-04-16 Impact factor: 5.262
Authors: Neal W Dickert; Victoria A Mah; Michelle H Biros; Deneil M Harney; Robert Silbergleit; Jeremy Sugarman; Emir Veledar; Kevin P Weinfurt; David W Wright; Rebecca D Pentz Journal: Crit Care Med Date: 2014-02 Impact factor: 7.598
Authors: Neal W Dickert; Kathleen Metz; Michael D Fetters; Adrianne N Haggins; Deneil K Harney; Candace D Speight; Robert Silbergleit Journal: Acad Emerg Med Date: 2021-05-26 Impact factor: 5.221