Improving the Informed Consent Process for Research Subjects with Low Literacy: A Systematic Review

ABSTRACTBACKGROUNDInadequate health literacy may impair research subjects’ ability to participate adequately in the informed consent (IC) process. Our aim is to evaluate the evidence supporting interventions, to improve comprehension of the IC process in low literacy subjects.METHODSWe performed a MEDLINE database search (1966 to November 2011) supplemented by manual searches of bibliographies of key relevant articles. We selected all studies in which a modification of the IC was tested to improve comprehension in low literacy populations. Study design, quality criteria, population, interventions and outcomes for each trial were extracted. The main outcome evaluated was comprehension, measured using a written test or verbal comprehension.RESULTSOur search strategy yielded 281 studies, of which only six met our eligibility criteria. The six studies included 1620 research participants. The studies predominantly included populations that were older (median age 61, range 48–64), ethnic minority, and with literacy level of 8th grade or below. Only one study had a randomized design. The specific intervention differed in each study. Two of the studies included the teach-back method or teach to goal method and achieved the highest level of comprehension. Two studies changed the readability level of the IC and resulted in the lowest comprehension among study subjects.CONCLUSIONSThe evidence supporting interventions to improve the informed consent process in low literacy populations is extremely limited. Among the interventions evaluated, having a study team member spend more time talking one-on-one to study participants was the most effective strategy for improving informed consent understanding; however, this finding is based on the results of a single study.

[1]  M. Egger,et al.  The hazards of scoring the quality of clinical trials for meta-analysis. , 1999, JAMA.

[2]  P. Raich,et al.  Literacy, Comprehension, and Informed Consent in Clinical Research , 2001, Cancer investigation.

[3]  D. DeMets,et al.  How informed is informed consent?: The BHAT experience , 1981 .

[4]  S. Chong,et al.  An assessment of the understanding and motivations of patients with schizophrenia about participating in a clinical trial. , 2009, Contemporary clinical trials.

[5]  H. Riecken,et al.  Informed consent to biomedical research in Veterans Administration Hospitals. , 1982, JAMA.

[6]  Michael K Paasche-Orlow,et al.  Readability standards for informed-consent forms as compared with actual readability. , 2003, The New England journal of medicine.

[7]  E. Marcus The silent epidemic--the health effects of illiteracy. , 2006, The New England journal of medicine.

[8]  Steven Joffe,et al.  Quality of informed consent in cancer clinical trials: a cross-sectional survey , 2001, The Lancet.

[9]  Jeremy Sugarman,et al.  Confirming comprehension of informed consent as a protection of human subjects , 2006, Journal of General Internal Medicine.

[10]  Sunil Kripalani,et al.  Clinical research in low-literacy populations: using teach-back to assess comprehension of informed consent and privacy information. , 2008, IRB.

[11]  C K Daugherty,et al.  Quantitative analysis of ethical issues in phase I trials: a survey interview of 144 advanced cancer patients. , 2000, IRB.

[12]  Nancy D Berkman,et al.  Literacy and health outcomes. A systematic review of the literature , 2004, Journal of general internal medicine.

[13]  J. Sugarman Missing the informed in consent. , 2003, Anesthesia and analgesia.

[14]  D. Schillinger,et al.  Use of a modified informed consent process among vulnerable patients: a descriptive study , 2007, Journal of General Internal Medicine.

[15]  James Flory,et al.  Interventions to improve research participants' understanding in informed consent for research: a systematic review. , 2004, JAMA.

[16]  G. Eckert,et al.  Health literacy in an adult dental research population: a pilot study. , 2008, Journal of public health dentistry.

[17]  Mark V. Williams,et al.  Health literacy and knowledge of chronic disease. , 2003, Patient education and counseling.

[18]  M. Wolf,et al.  The causal pathways linking health literacy to health outcomes. , 2007, American journal of health behavior.

[19]  R. Holcombe,et al.  Informed consent for clinical trials: a comparative study of standard versus simplified forms. , 1998, Journal of the National Cancer Institute.

[20]  Laura M. Pfeifer,et al.  Using computer agents to explain medical documents to patients with low health literacy. , 2009, Patient education and counseling.

[21]  F. E. Freeberg,et al.  Informed consent documents: increasing comprehension by reducing reading level. , 1990, IRB.

[22]  M. Wolf,et al.  Health literacy and health risk behaviors among older adults. , 2007, American journal of preventive medicine.