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Items: 1 to 20 of 102


What information and the extent of information research participants need in informed consent forms: a multi-country survey.

Karbwang J, Koonrungsesomboon N, Torres CE, Jimenez EB, Kaur G, Mathur R, Sholikhah EN, Wanigatunge C, Wong CS, Yimtae K, Abdul Malek M, Ahamad Fouzi L, Ali A, Chan BZ, Chandratilake M, Chiew SC, Chin MYC, Gamage M, Gitek I, Hakimi M, Hussin N, Jamil MFA, Janarsan P, Julia M, Kanungo S, Karunanayake P, Kollanthavelu S, Kong KK, Kueh BL, Kulkarni R, Kumaran PP, Kumarasiri R, Lim WH, Lim XJ, Mahmud F, Mantaring JBV 3rd, Md Ali SM, Mohd Noor N, Muhunthan K, Nagandran E, Noor M, Ooi KH, Pradeepan JA, Sadewa AH, Samaranayake N, Sri Ranganathan S, Subasingha W, Subramaniam S, Sulaiman N, Tay JF, Teng LH, Tew MM, Tharavanij T, Tok PSK, Weeratna J, Wibawa T, Wickremasinghe R, Wongwai P, Yadav S; FERCAP Multi-Country Research Team.

BMC Med Ethics. 2018 Sep 15;19(1):79. doi: 10.1186/s12910-018-0318-x.


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.


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.


Improved participants' understanding in a healthy volunteer study using the SIDCER informed consent form: a randomized-controlled study.

Koonrungsesomboon N, Teekachunhatean S, Hanprasertpong N, Laothavorn J, Na-Bangchang K, Karbwang J.

Eur J Clin Pharmacol. 2016 Apr;72(4):413-21. doi: 10.1007/s00228-015-2000-2. Epub 2015 Dec 29.


SIDCER informed consent form: principles and a developmental guideline.

Koonrungsesomboon N, Laothavorn J, Chokevivat V, Hirayama K, Karbwang J.

Indian J Med Ethics. 2016 Apr-Jun;1(2):83-6. Epub 2016 Feb 29.


Giving consent without getting informed: a cross-cultural issue in research ethics.

Ghandour L, Yasmine R, El-Kak F.

J Empir Res Hum Res Ethics. 2013 Jul;8(3):12-21. doi: 10.1525/jer.2013.8.3.12.


Moving Forward on Consent Practices in Australia.

McWhirter RE, Eckstein L.

J Bioeth Inq. 2018 Jun;15(2):243-257. doi: 10.1007/s11673-018-9843-z. Epub 2018 Mar 12.


Getting meaningful informed consent from older adults: a structured literature review of empirical research.

Sugarman J, McCrory DC, Hubal RC.

J Am Geriatr Soc. 1998 Apr;46(4):517-24. Review.


Assessing decisional capacity for research participation in psychiatric patients and their relatives.

George DE, Dholakia S, Tharyan P.

Indian J Med Ethics. 2018 Apr-Jun;3(2):125-133. doi: 10.20529/IJME.2017.075. Epub 2017 Aug 8.


Evidence-Based Strategies for Shortening Informed Consent Forms in Clinical Research.

Corneli A, Namey E, Mueller MP, Tharaldson J, Sortijas S, Grey T, Sugarman J.

J Empir Res Hum Res Ethics. 2017 Feb;12(1):14-25. doi: 10.1177/1556264616682550. Epub 2017 Jan 12.


The adequacy of informed consent forms in genetic research in Oman: a pilot study.

Al-Riyami A, Jaju D, Jaju S, Silverman HJ.

Dev World Bioeth. 2011 Aug;11(2):57-62. doi: 10.1111/j.1471-8847.2010.00293.x. Epub 2011 Jan 25.


Critical evaluation of informed consent forms for adult and minor aged whole blood donation used by United States blood centers.

Shaz BH, Demmons DG, Hillyer CD.

Transfusion. 2009 Jun;49(6):1136-45. doi: 10.1111/j.1537-2995.2009.02093.x. Epub 2009 Feb 9.


The effectiveness of health literacy interventions on the informed consent process of health care users: a systematic review protocol.

Perrenoud B, Velonaki VS, Bodenmann P, Ramelet AS.

JBI Database System Rev Implement Rep. 2015 Oct;13(10):82-94. doi: 10.11124/jbisrir-2015-2304.


Informed consent form challenges for genetic research in a developing Arab country with high risk for genetic disease.

Nair SC, Ibrahim H.

J Genet Couns. 2015 Apr;24(2):294-9. doi: 10.1007/s10897-014-9763-y. Epub 2014 Sep 18.


Informed Consent to Study Purpose in Randomized Clinical Trials of Antibiotics, 1991 Through 2011.

Doshi P, Hur P, Jones M, Albarmawi H, Jefferson T, Morgan DJ, Spears PA, Powers JH 3rd.

JAMA Intern Med. 2017 Oct 1;177(10):1452-1459. doi: 10.1001/jamainternmed.2017.3820.


A Comparison of the Quality of Informed Consent for Clinical Trials of an Experimental Hookworm Vaccine Conducted in Developed and Developing Countries.

Diemert DJ, Lobato L, Styczynski A, Zumer M, Soares A, Gazzinelli MF.

PLoS Negl Trop Dis. 2017 Jan 23;11(1):e0005327. doi: 10.1371/journal.pntd.0005327. eCollection 2017 Jan.


"It's my blood": ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants.

Moodley K, Sibanda N, February K, Rossouw T.

BMC Med Ethics. 2014 Jan 22;15:4. doi: 10.1186/1472-6939-15-4.


Comparison of participant information and informed consent forms of five European studies in genetic isolated populations.

Mascalzoni D, Janssens AC, Stewart A, Pramstaller P, Gyllensten U, Rudan I, van Duijn CM, Wilson JF, Campbell H, Quillan RM; EUROSPAN consortium.

Eur J Hum Genet. 2010 Mar;18(3):296-302. doi: 10.1038/ejhg.2009.155. Epub 2009 Oct 14.


[Quality and legibility of written informed consent form in pharmacogenetic research].

Ruiz Ramos J, Cueto-Sola M, García Robles A, Pérez Huertas P, Tordera Baviera M, Poveda Andrés JL.

Cuad Bioet. 2015 Jan-Apr;26(86):129-38. Spanish.

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