What information and the extent of information research participants need in informed consent forms: a multi-country survey
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Published:2018-09-15
Issue:1
Volume:19
Page:
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ISSN:1472-6939
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Container-title:BMC Medical Ethics
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language:en
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Short-container-title:BMC Med Ethics
Author:
Karbwang Juntra, , Koonrungsesomboon NutORCID, Torres Cristina E., Jimenez Edlyn B., Kaur Gurpreet, Mathur Roli, Sholikhah Eti N., Wanigatunge Chandanie, Wong Chih-Shung, Yimtae Kwanchanok, Abdul Malek Murnilina, Ahamad Fouzi Liyana, Ali Aisyah, Chan Beng Z., Chandratilake Madawa, Chiew Shoen C., Chin Melvyn Y. C., Gamage Manori, Gitek Irene, Hakimi Mohammad, Hussin Narwani, Jamil Mohd F. A., Janarsan Pavithra, Julia Madarina, Kanungo Suman, Karunanayake Panduka, Kollanthavelu Sattian, Kong Kian K., Kueh Bing-Ling, Kulkarni Ragini, Kumaran Paul P., Kumarasiri Ranjith, Lim Wei H., Lim Xin J., Mahmud Fatihah, Mantaring Jacinto B. V., Md Ali Siti M., Mohd Noor Nurain, Muhunthan Kopalasuntharam, Nagandran Elanngovan, Noor Maisarah, Ooi Kim H., Pradeepan Jebananthy A., Sadewa Ahmad H., Samaranayake Nilakshi, Sri Ranganathan Shalini, Subasingha Wasanthi, Subramaniam Sivasangari, Sulaiman Nadirah, Tay Ju F., Teng Leh H., Tew Mei M., Tharavanij Thipaporn, Tok Peter S. K., Weeratna Jayanie, Wibawa Tri, Wickremasinghe Renu, Wongwai Phanthipha, Yadav Subhash
Funder
Forum for Ethical Review Committees in the Asian and Western Pacific region Research Grant under Adhoc Research Scheme from Indian Council of Medical Research Faculty of Medicine Universitas Gadjah Mada Grants Philippine Health Research Ethics Network
Publisher
Springer Science and Business Media LLC
Subject
Health Policy,Health (social science),Issues, ethics and legal aspects
Reference48 articles.
1. World Medical Association. World medical association declaration of Helsinki: ethical principles for medical research involving human subjects. JAMA. 2013;310:2191–4. 2. Guideline for good clinical practice E6(R2). European Medicines Agency. Available from:
http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2009/09/WC500002874.pdf
. Accessed 15 Feb 2018. 3. Berger O, Grønberg BH, Sand K, Kaasa S, Loge JH. The length of consent documents in oncological trials is doubled in twenty years. Ann Oncol. 2009;20:379–85. 4. Kass NE, Chaisson L, Taylor HA, Lohse J. Length and complexity of US and international HIV consent forms from federal HIV network trials. J Gen Intern Med. 2011;26:1324–8. 5. Ménoni V, Lucas N, Leforestier JF, et al. The readability of information and consent forms in clinical research in France. PLoS One. 2010;5:e10576.
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