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Items: 1 to 20 of 131

1.

Randomization to standard and concise informed consent forms: development of evidence-based consent practices.

Enama ME, Hu Z, Gordon I, Costner P, Ledgerwood JE, Grady C; VRC 306 and 307 Consent Study Teams.

Contemp Clin Trials. 2012 Sep;33(5):895-902. Epub 2012 Apr 20.

2.

A randomized trial comparing concise and standard consent forms in the START trial.

Grady C, Touloumi G, Walker AS, Smolskis M, Sharma S, Babiker AG, Pantazis N, Tavel J, Florence E, Sanchez A, Hudson F, Papadopoulos A, Emanuel E, Clewett M, Munroe D, Denning E; INSIGHT START Informed Consent Substudy Group.

PLoS One. 2017 Apr 26;12(4):e0172607. doi: 10.1371/journal.pone.0172607. eCollection 2017.

3.

Interactive informed consent: randomized comparison with paper consents.

Rowbotham MC, Astin J, Greene K, Cummings SR.

PLoS One. 2013;8(3):e58603. doi: 10.1371/journal.pone.0058603. Epub 2013 Mar 6.

4.

Satisfying the needs of Japanese cancer patients: a comparative study of detailed and standard informed consent documents.

Sato K, Watanabe T, Katsumata N, Sato T, Ohashi Y.

Clin Trials. 2014 Feb;11(1):86-95. doi: 10.1177/1740774513515550. Epub 2014 Jan 9.

PMID:
24408900
5.

A randomized controlled trial of short and standard-length consent forms for a genetic cohort study: is longer better?

Matsui K, Lie RK, Turin TC, Kita Y.

J Epidemiol. 2012;22(4):308-16. Epub 2012 Mar 24.

6.

A rural community's involvement in the design and usability testing of a computer-based informed consent process for the Personalized Medicine Research Project.

Mahnke AN, Plasek JM, Hoffman DG, Partridge NS, Foth WS, Waudby CJ, Rasmussen LV, McManus VD, McCarty CA.

Am J Med Genet A. 2014 Jan;164A(1):129-40. doi: 10.1002/ajmg.a.36220. Epub 2013 Nov 22.

7.

A booklet on participants' rights to improve consent for clinical research: a randomized trial.

Benatar JR, Mortimer J, Stretton M, Stewart RA.

PLoS One. 2012;7(10):e47023. doi: 10.1371/journal.pone.0047023. Epub 2012 Oct 19.

8.

Improved informed consent documents for biomedical research do not increase patients' understanding but reduce enrolment: a study in real settings.

Paris A, Deygas B, Cornu C, Thalamas C, Maison P, Duale C, Kane M, Hodaj E, Cracowski JL.

Br J Clin Pharmacol. 2015 Nov;80(5):1010-20. doi: 10.1111/bcp.12716. Epub 2015 Sep 21.

9.
10.

Informed Consent-Uninformed Participants: Shortcomings of Online Social Science Consent Forms and Recommendations for Improvement.

Perrault EK, Nazione SA.

J Empir Res Hum Res Ethics. 2016 Jul;11(3):274-80. doi: 10.1177/1556264616654610. Epub 2016 Jun 21.

PMID:
27329533
11.
12.

Improvement of informed consent and the quality of consent documents.

Jefford M, Moore R.

Lancet Oncol. 2008 May;9(5):485-93. doi: 10.1016/S1470-2045(08)70128-1. Review.

PMID:
18452859
13.

Undergraduate Consent Form Reading in Relation to Conscientiousness, Procrastination, and the Point-of-Time Effect.

Theiss JD, Hobbs WB, Giordano PJ, Brunson OM.

J Empir Res Hum Res Ethics. 2014 Jul;9(3):11-7. doi: 10.1177/1556264614540593.

PMID:
25746782
14.

[Readability of informed consent forms for subjects participating in biomedical research: updating is required].

Paris A, Cracowski JL, Ravanel N, Cornu C, Gueyffier F, Deygas B, Guillot K, Bosson JL, Hommel M.

Presse Med. 2005 Jan 15;34(1):13-8. French.

15.

Comprehension of Randomization and Uncertainty in Cancer Clinical Trials Decision Making Among Rural, Appalachian Patients.

Krieger JL, Palmer-Wackerly A, Dailey PM, Krok-Schoen JL, Schoenberg NE, Paskett ED.

J Cancer Educ. 2015 Dec;30(4):743-8. doi: 10.1007/s13187-015-0789-0.

16.

Informed consent for research: a study to evaluate readability and processability to effect change.

Philipson SJ, Doyle MA, Gabram SG, Nightingale C, Philipson EH.

J Investig Med. 1995 Oct;43(5):459-67.

PMID:
8528757
17.

Should consent forms used in clinical trials be translated into the local dialects? A survey among past participants in rural Ghana.

Baiden F, Akazili J, Chatio S, Achana FS, Oduro AR, Ravinetto R, Hodgson A.

Clin Trials. 2016 Apr;13(2):234-9. doi: 10.1177/1740774515609290. Epub 2015 Oct 9.

PMID:
26452387
18.

Simplification improves understanding of informed consent information in clinical trials regardless of health literacy level.

Kim EJ, Kim SH.

Clin Trials. 2015 Jun;12(3):232-6. doi: 10.1177/1740774515571139. Epub 2015 Feb 19.

PMID:
25701156
20.

Improved participants' understanding of research information in real settings using the SIDCER informed consent form: a randomized-controlled informed consent study nested with eight clinical trials.

Koonrungsesomboon N, Tharavanij T, Phiphatpatthamaamphan K, Vilaichone RK, Manuwong S, Curry P, Siramolpiwat S, Punchaipornpon T, Kanitnate S, Tammachote N, Yamprasert R, Chanvimalueng W, Kaewkumpai R, Netanong S, Kitipawong P, Sritipsukho P, Karbwang J.

Eur J Clin Pharmacol. 2017 Feb;73(2):141-149. doi: 10.1007/s00228-016-2159-1. Epub 2016 Nov 12.

PMID:
27838760

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