Abstract
GlaxoSmithKline (formerly Glaxo Wellcome Genetics Directorate) undertook a descriptive study to elicit volunteers’ perceptions of a pharmacogenetic research consent form, an educational brochure, and a video; and to identify modifications in these materials that would enhance their usefulness. Face-to-face interviews were conducted to obtain feedback on the material and assess volunteer understanding of the basic components of the study. Although repeated exposure to key information in different formats resulted in improved comprehension, almost one-third of respondents could not accurately describe the two options for participating in the pharmacogenetic research. Almost all of the respondents reported that they would like to have the brochure, video, or both, in addition to the consent form. These results underscore the importance of providing volunteers with the opportunity for discussion with the study physician. They also support the use of supplementary aids to accommodate different styles of processing information. The respondents’ suggestions will be considered when the materials are revised.
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References
- 1.
Rapoport DM. Consent process. Reg Aff Focus. July 2000;7–3.
- 2.
President’s Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral Research. Protecting Human Subjects. Washington, DC: US Government Printing Office; 1981.
- 3.
National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. The Belmont Report: Ethical principles and guidelines for the protection of human subjects of research. Washington, DC: US Government Printing Office; 1988.
- 4.
Protection of Human Subjects. 46 Federal Register. 8386 (1981) (codified at 45 CFR §46).
- 5.
Reilly PR, Boshar MF, Holtzman SH. Ethical issues in genetic research: Disclosure and informed consent. Nature Genetics. 1997;15:16–20.
- 6.
Meade CD. Improving understanding of the in-formed consent document. Semin Oncol Nurs. May 1999;15:124–137.
- 7.
White LJ, Jones JS, Felton CW, Pool LC. Informed consent for medical research: Common discrepancies and readability. Acad Emerg Med. 1996;3:745–750.
- 8.
Philipson SJ, Doyle MA, Gabram SGA, Nightingale C, Philipson EH. Informed consent for research: A study to evaluate readability and processability to effect change. J Investig Med. 1995;43:459–467.
- 9.
Tankanow RM, Burgunda VS, Weiskopf JA. Patients’ perceived understanding of informed consent in investigational drug studies. Am J Hosp Pharm. 1992;49:633–635.
- 10.
Verheggen FWSM, Jonkers R, Kok G. Patients’ perceptions on informed consent and the quality of information disclosure in clinical trials. Patient Educ Counsel. 1996;29:137–153.
- 11.
Harris KA. The informational needs of patients with cancer and their families. Cancer Pract. 1998;6:39–46.
- 12.
Hinds C, Streater A, Mood D. Functions and preferred methods of receiving information related to radiotherapy. Cancer Nurs. 1995;5:374–384.
- 13.
Silva MC, Sorrell JM. Enhancing comprehension of information for informed consent: A review of empirical research. IRB: A Review Human Subjects Research. Jan/Feb 1988;10:1–5.
- 14.
Shmerling A, Schattner P, Piterman L. Qualitative research in medical practice. Med J Aust. 1993;158:619–622.
- 15.
Protection of Human Subjects. 46 Federal Register. 8951 (1981), as amended at 61 Federal Register. 57289 (1996) (codified at 21 CFR §50).
- 16.
Agre P, McKee K, Gargon N, et al. Patient satisfaction with an informed consent process. Cancer Pract. 1997;5:62–67.
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McPherson, E.C., Ray, S.C., Rieser, P.A. et al. Pharmacogenetic Research: Perceptions of Informed Consent. Ther Innov Regul Sci 36, 83–93 (2002). https://doi.org/10.1177/009286150203600113
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Key Words
- Informed consent
- Descriptive study
- Pharmacogenetic research
- Written and audiovisual materials for informed consent
- Perceptions of informed consent