Informed Consent Form Challenges for Genetic Research in a Developing Arab Country with High Risk for Genetic Disease

被引:5
|
作者
Nair, Satish Chandrasekhar [1 ]
Ibrahim, Halah [1 ]
机构
[1] Johns Hopkins Med USA, Dept Acad Affairs, Med Affairs, Tawam Hosp, Al Ain, U Arab Emirates
关键词
Informed consent; Readability; Good clinical practice compliance; Genetic research; DISORDERS; MUTATIONS;
D O I
10.1007/s10897-014-9763-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The prevalence of genetic disease is high in the Middle East, particularly in the United Arab Emirates. Our study assesses the information provided in, and the readability ease of, informed consent forms (ICF) for genetic research studies. A multicenter retrospective cross-sectional review of 54 ICFs was conducted to assess compliance by comparing them with standard good clinical practice guidelines for developing consent forms. Readability of the forms was determined using the Flesch-Kincaid scale. Overall Good Clinical Practice compliance for the ICFs averaged at 63 %. Information regarding privacy, confidentiality, specimen collection and storage were absent from the majority of the ICFs. Readability ease score was low (36.7 +/- 4.6) and required college-level (11.8 +/- 1.4) reading skills to understand the information. Our study highlights the need to improve the readability and information contained in the ICFs for genetic research studies in our setting. Our findings may be generalized to similar cultures in the Middle East and Asia.
引用
收藏
页码:294 / 299
页数:6
相关论文
共 50 条
  • [21] Tailoring the process of informed consent in genetic and genomic research
    Rotimi, Charles N.
    Marshall, Patricia A.
    GENOME MEDICINE, 2010, 2
  • [22] Voluntary participation and informed consent to international genetic research
    Marshall, Patricia A.
    Adebamowo, Clement A.
    Adeyemo, Adebowale A.
    Ogundiran, Temidayo O.
    Vekich, Mirjana
    Strenski, Teri
    Zhou, Jie
    Prewitt, T. Elaine
    Cooper, Richard S.
    Rotimi, Charles N.
    AMERICAN JOURNAL OF PUBLIC HEALTH, 2006, 96 (11) : 1989 - 1995
  • [23] The end of informed consent -: The informed contract in genetic research and public health
    Schröder, P
    GESUNDHEITSWESEN, 2004, 66 (8-9) : 631 - 631
  • [24] Genetic research as therapy: Implications of "gene therapy" for informed consent
    Churchill, LR
    Collins, ML
    King, NMP
    Pemberton, SG
    Wailoo, KA
    JOURNAL OF LAW MEDICINE & ETHICS, 1998, 26 (01): : 38 - 47
  • [25] Ethical issues and informed consent in psychiatric genetic research.
    Shore, D
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 74 (06): : 593 - 593
  • [26] Patients' Views on Identifiability of Samples and Informed Consent for Genetic Research
    Hull, Sara Chandros
    Sharp, Richard R.
    Botkin, Jeffrey R.
    Brown, Mark
    Hughes, Mark
    Sugarman, Jeremy
    Schwinn, Debra
    Sankar, Pamela
    Bolcic-Jankovic, Dragana
    Clarridge, Brian R.
    Wilfond, Benjamin S.
    Katz, Treuman
    AMERICAN JOURNAL OF BIOETHICS, 2008, 8 (10): : 62 - 70
  • [27] Examining the adequacy of preoperative informed consent in a developing country: Challenges in the era of surgical specialisation
    Ede, Osita
    Obadaseraye, Oke R.
    Anichi, Ifeanyi
    Mbaeze, Chisom
    Udemezue, Chukwuka O.
    Basil-Nwachuku, Chinonso
    Madu, Kenechi A.
    Iyidobi, Emmanuel C.
    Anyaehie, Udo E.
    Nwadinigwe, Cajetan U.
    Ngwangwa, Chidinma
    Adetula, Uto Essien
    DEVELOPING WORLD BIOETHICS, 2024, 24 (04) : 296 - 301
  • [28] Informed Consent for Exome Sequencing Research in Families with Genetic Disease: The Emerging Issue of Incidental Findings
    Bergner, Amanda L.
    Bollinger, Juli
    Raraigh, Karen S.
    Tichnell, Crystal
    Murray, Brittney
    Blout, Carrie Lynn
    Telegrafi, Aida Bytyci
    James, Cynthia A.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (11) : 2745 - 2752
  • [29] A dynamic informed consent process for population based genetic research.
    Smith, ME
    Manasco, PK
    Arledge, T
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 380 - 380
  • [30] THE ADEQUACY OF INFORMED CONSENT FORMS IN GENETIC RESEARCH IN OMAN: A PILOT STUDY
    Al-Riyami, Asya
    Jaju, Deepali
    Jaju, Sanjay
    Silverman, Henry J.
    DEVELOPING WORLD BIOETHICS, 2011, 11 (02) : 57 - 62