Readability of model consent forms provided by IRBs

被引:0
|
作者
Riley, K [1 ]
Mackiewicz, J [1 ]
机构
[1] Univ Minnesota, Duluth, MN 55812 USA
关键词
D O I
暂无
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Institutional review boards (IRBs) often provide model consent forms for researchers to use or adapt when conducting human subjects research. However, the models themselves often far exceed the 8th-grade reading level recommended for consent forms, with many models measuring grade 12 or higher. In this paper, we look specifically at how much, and how, model consent forms deviate from the desired 8th-grade reading level, as measured by the Flesch Reading Ease formula and the Flesch-Kincaid Grade Level formula. We discuss quantifiable features measurable by these formulas and by text analysis features available in Microsoft Word (e.g., sentence length, paragraph length, and percentage of passive voice sentences). We outline plans to examine additional features such as nominalization, patterns in the flow of given and new information, and document design. Our findings are designed to help IRBs and researchers prepare consent forms that are more readable and, therefore, more in keeping with legal and ethical guidelines for human subjects research.
引用
收藏
页码:145 / 157
页数:13
相关论文
共 50 条
  • [21] Assessing the readability statistics of national consent forms in the UK
    Williamson, J. M. L.
    Martin, A. G.
    [J]. INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2010, 64 (03) : 322 - 329
  • [22] 2 FORMULAS FOR DETERMINING READABILITY OF SUBJECT CONSENT FORMS
    GRUNDNER, TM
    [J]. AMERICAN PSYCHOLOGIST, 1978, 33 (08) : 773 - 775
  • [23] PREHOSPITAL IRBS AND CONSENT - REPLY
    KIM, DT
    [J]. ANNALS OF EMERGENCY MEDICINE, 1994, 24 (04) : 760 - 760
  • [24] USE, CONTENT, AND READABILITY OF WRITTEN INFORMED CONSENT FORMS FOR TREATMENT
    HANDELSMAN, MM
    KEMPER, MB
    KESSONCRAIG, P
    MCLAIN, J
    JOHNSRUD, C
    [J]. PROFESSIONAL PSYCHOLOGY-RESEARCH AND PRACTICE, 1986, 17 (06) : 514 - 518
  • [25] Cancer clinical trial consent forms: A readability analysis.
    Roy, Mohana
    Schapira, Lidia
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2020, 38 (15)
  • [26] Readability of informed consent forms for whole exome/genome sequencing
    Niemiec, E.
    Vears, D.
    Borry, P.
    Howard, H. C.
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 814 - 815
  • [27] Assessing the Readability of Clinical Trial Consent Forms for Surgical Specialties
    Karimi, Amir H.
    Guyler, Maura R.
    Hecht II, Christian J.
    Burkhart, Robert J.
    Acuna, Alexander J.
    Kamath, Atul F.
    [J]. JOURNAL OF SURGICAL RESEARCH, 2024, 296 : 711 - 719
  • [28] A comprehensive analysis of the readability of consent forms for blood transfusion in Spain
    Morales-Valdivia, Estela
    Brady, Anne-Marie
    Mariscal-Crespo, Maria I.
    Camacho-Bejarano, Rafaela
    [J]. BLOOD TRANSFUSION, 2023, 21 (04) : 356 - 363
  • [29] The Contents and Readability of Informed Consent Forms for Oncology Clinical Trials
    Cheung, Winson Y.
    Pond, Gregory R.
    Heslegrave, Ronald J.
    Enright, Katherine
    Potanina, Larissa
    Siu, Lillian L.
    [J]. AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2010, 33 (04): : 387 - 392
  • [30] Evaluation of patients' inform consent forms in oncology: readability of the information
    Ertem-Vehid, Hayriye
    Giresunlu, I. Mufit
    Koksalan, Hilal
    [J]. TURK ONKOLOJI DERGISI-TURKISH JOURNAL OF ONCOLOGY, 2006, 21 (04): : 187 - 190