Elaine L Larson1, Rachel Lally2, Gabriella Foe3, Gabriela Joaquin4, Dodi D Meyer5, Elizabeth G Cohn6,7. 1. School of Nursing, Mailman School of Public Health, Columbia University, New York, New York, USA. 2. Human Research Protection Office, Columbia University, New York, New York, USA. 3. School of Continuing Studies, Columbia University, New York, New York, USA. 4. The City College of New York, New York, New York, USA. 5. Community Pediatrics, College of Physicians and Surgeons, Columbia University, New York, New York, USA. 6. Center for Health Innovation, Adelphi University, Garden City, New York, USA. 7. School of Nursing, Columbia University, New York, New York, USA.
Abstract
OBJECTIVE: To describe the development and testing of a module to improve consent administrators' skills when obtaining research consent from culturally and linguistically diverse and low literacy populations. DESIGN: Development and psychometric testing of video module including community vignettes. METHODS: Following initial content, face, and construct validity testing by experts, a field trial was conducted with pre- and postknowledge tests and satisfaction surveys completed by 112 consent administrators. RESULTS: Mean score out of a possible 10 on pretest was 8.6 (±standard deviation [SD], 1.55) and on posttest was 9.1 (±SD, 1.2; paired t-test 95% confidence interval of difference: -0.18 to -0.88; two-tailed p = 0.003). The average years of experience with obtaining consent was 6.42 years (range: 0-35), but years of experience was not significantly associated with either pre- or posttest scores (p = 0.82 and 0.44, respectively). Most user evaluations were positive, although suggestions for improvements were made. CONCLUSION: Although pretest scores were relatively high, training needs of research consent administrators for consenting diverse and low literacy populations may be unmet. We urge that institutional review boards, researchers, policymakers, educators, and bioethicists address the training needs of research consent administrators and we offer this training module as one potential resource and adjunct to such training.
OBJECTIVE: To describe the development and testing of a module to improve consent administrators' skills when obtaining research consent from culturally and linguistically diverse and low literacy populations. DESIGN: Development and psychometric testing of video module including community vignettes. METHODS: Following initial content, face, and construct validity testing by experts, a field trial was conducted with pre- and postknowledge tests and satisfaction surveys completed by 112 consent administrators. RESULTS: Mean score out of a possible 10 on pretest was 8.6 (±standard deviation [SD], 1.55) and on posttest was 9.1 (±SD, 1.2; paired t-test 95% confidence interval of difference: -0.18 to -0.88; two-tailed p = 0.003). The average years of experience with obtaining consent was 6.42 years (range: 0-35), but years of experience was not significantly associated with either pre- or posttest scores (p = 0.82 and 0.44, respectively). Most user evaluations were positive, although suggestions for improvements were made. CONCLUSION: Although pretest scores were relatively high, training needs of research consent administrators for consenting diverse and low literacy populations may be unmet. We urge that institutional review boards, researchers, policymakers, educators, and bioethicists address the training needs of research consent administrators and we offer this training module as one potential resource and adjunct to such training.
Authors: Adam Nishimura; Jantey Carey; Patricia J Erwin; Jon C Tilburt; M Hassan Murad; Jennifer B McCormick Journal: BMC Med Ethics Date: 2013-07-23 Impact factor: 2.652