-
1
-
-
4644281540
-
Interventions to improve research participants' understanding in informed consent: a systematic review
-
Florey J, Emmanuel E. Interventions to improve research participants' understanding in informed consent: a systematic review. JAMA (2004) 292(20):2201-4. doi:10.1001/jama.292.13.1593
-
(2004)
JAMA
, vol.292
, Issue.20
, pp. 2201-2204
-
-
Florey, J.1
Emmanuel, E.2
-
2
-
-
10044248733
-
Consent documents for oncology trials: does anybody read these things?
-
Sharp SM. Consent documents for oncology trials: does anybody read these things? Am J Clin Oncol (2004) 27(6):570-5. doi:10.1097/01.coc.0000135925.83221.b3
-
(2004)
Am J Clin Oncol
, vol.27
, Issue.6
, pp. 570-575
-
-
Sharp, S.M.1
-
3
-
-
84973780641
-
Writing readable informed consent forms
-
Zanecchia D. Writing readable informed consent forms. Appl Clin Trials (1992) 1:52-62
-
(1992)
Appl Clin Trials
, vol.1
, pp. 52-62
-
-
Zanecchia, D.1
-
4
-
-
85061984836
-
Writing, reading and understanding research consent forms
-
Hochhauser M. Writing, reading and understanding research consent forms. Appl Clin Trials (1997) 6:66-73
-
(1997)
Appl Clin Trials
, vol.6
, pp. 66-73
-
-
Hochhauser, M.1
-
5
-
-
84996183964
-
The informed consent form: document development and evaluation
-
Hochhauser M. The informed consent form: document development and evaluation. Ther Innov Regul Sci (2000) 34(4):1309-17. doi:10.1177/009286150003400438
-
(2000)
Ther Innov Regul Sci
, vol.34
, Issue.4
, pp. 1309-1317
-
-
Hochhauser, M.1
-
6
-
-
80054953755
-
-
1st ed. In: Seyberth H, Rane A, Schwab M, editors. Pediatric Clinical Pharmacology. Heidelberg: Springer
-
Roth-Cline M, Gerson J, Bright P, Lee C, Nelson RM. Ethical considerations in conducting paediatric research. 1st ed. In: Seyberth H, Rane A, Schwab M, editors. Pediatric Clinical Pharmacology. Heidelberg: Springer (2011). p. 219-44
-
(2011)
Ethical considerations in conducting paediatric research
, pp. 219-244
-
-
Roth-Cline, M.1
Gerson, J.2
Bright, P.3
Lee, C.4
Nelson, R.M.5
-
8
-
-
34047223877
-
Longer consent forms for clinical trials compromise patient understanding: so why are they lengthening?
-
Beardsley E, Jefford M, Mileshkin L. Longer consent forms for clinical trials compromise patient understanding: so why are they lengthening? J Clin Oncol (2007) 25(9):e13-4. doi:10.1200/JCO.2006.10.3341
-
(2007)
J Clin Oncol
, vol.25
, Issue.9
, pp. e13-e14
-
-
Beardsley, E.1
Jefford, M.2
Mileshkin, L.3
-
9
-
-
77954015517
-
The evolution of consent forms for research: a quarter century of changes
-
Albala L, Doyle M, Appelbaum PS. The evolution of consent forms for research: a quarter century of changes. IRB (2010) 32(3):7-11
-
(2010)
IRB
, vol.32
, Issue.3
, pp. 7-11
-
-
Albala, L.1
Doyle, M.2
Appelbaum, P.S.3
-
11
-
-
0022575365
-
Response of patients to informed consent for excretory urography
-
Winfield AC, Ford CV, James AE, Heller RM, Lamballe AK. Response of patients to informed consent for excretory urography. Urol Radiol (1986) 8(1):35-9. doi:10.1007/BF02924069
-
(1986)
Urol Radiol
, vol.8
, Issue.1
, pp. 35-39
-
-
Winfield, A.C.1
Ford, C.V.2
James, A.E.3
Heller, R.M.4
Lamballe, A.K.5
-
12
-
-
85061988452
-
-
Australian Bureau of Statistics. Programme for the International Assessment of Adult Competencies (2007). Available from: http://www.innovation.gov.au/skills/ResourcesAndPublications/ ProgrammeForTheInternationalAssessmentOfAdultCompetencies/Pages/default.aspx
-
(2007)
Programme for the International Assessment of Adult Competencies
-
-
-
13
-
-
42549109855
-
Clinical research in low-literacy populations: using teach-back to assess comprehension of informed consent and privacy information
-
Kripalani S, Bengtzen R, Henerson L, Jacobson TA. Clinical research in low-literacy populations: using teach-back to assess comprehension of informed consent and privacy information. IRB (2008) 30(2):13-9
-
(2008)
IRB
, vol.30
, Issue.2
, pp. 13-19
-
-
Kripalani, S.1
Bengtzen, R.2
Henerson, L.3
Jacobson, T.A.4
-
15
-
-
0034737962
-
What makes clinical research ethical?
-
Emanuel E, Wendler D, Grady C. What makes clinical research ethical? JAMA (2000) 283(20):2701-11. doi:10.1001/jama.283.20.2701
-
(2000)
JAMA
, vol.283
, Issue.20
, pp. 2701-2711
-
-
Emanuel, E.1
Wendler, D.2
Grady, C.3
-
16
-
-
28244436787
-
Informed consent process: a survey of subjects assesses strengths and weaknesses
-
Getz KA. Informed consent process: a survey of subjects assesses strengths and weaknesses. Appl Clin Trials (2002) 30-6
-
(2002)
Appl Clin Trials
, pp. 30-36
-
-
Getz, K.A.1
-
17
-
-
84873109809
-
Readability and comprehensibility of informed consent forms for clinical trials
-
Pandiva A. Readability and comprehensibility of informed consent forms for clinical trials. Perspect Clin Res (2010) 1(3):98-100
-
(2010)
Perspect Clin Res
, vol.1
, Issue.3
, pp. 98-100
-
-
Pandiva, A.1
-
18
-
-
0030096941
-
An ethical assessment of researchers' description of the consenting process
-
Titus SL, Keane MA. An ethical assessment of researchers' description of the consenting process. J Clin Ethics (1996) 7:60-8
-
(1996)
J Clin Ethics
, vol.7
, pp. 60-68
-
-
Titus, S.L.1
Keane, M.A.2
-
20
-
-
85061996080
-
Safer Practice for Better Healthcare
-
Kizer KW, Blum LN. Safer Practice for Better Healthcare. Agency for Healthcare Research and Quality (2005). Available from: http://www.ahrq.gov/professionals/quality-patient-safety/patient-safety-resources/resources/nqfpract.pdf
-
(2005)
Agency for Healthcare Research and Quality
-
-
Kizer, K.W.1
Blum, L.N.2
-
22
-
-
42549095453
-
Use of consent forms and interactive questions in the consent process
-
Palmer BW, Cassidy EL, Dunn LB, Spira AP, Sheikh JI. Use of consent forms and interactive questions in the consent process. IRB (2008) 30(2):8-12
-
(2008)
IRB
, vol.30
, Issue.2
, pp. 8-12
-
-
Palmer, B.W.1
Cassidy, E.L.2
Dunn, L.B.3
Spira, A.P.4
Sheikh, J.I.5
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