Treatments for Neurodevelopmental Disorders: Evidence, Advocacy, and the Internet

Research output: Contribution to journalJournal articleResearchpeer-review

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Treatments for Neurodevelopmental Disorders : Evidence, Advocacy, and the Internet. / Di Pietro, Nina C; Whiteley, Louise Emma; Mizgalewicz, Ania; Illes, Judy.

In: Journal of Autism and Developmental Disorders, Vol. 43, No. 1, 2013, p. 122-133.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Di Pietro, NC, Whiteley, LE, Mizgalewicz, A & Illes, J 2013, 'Treatments for Neurodevelopmental Disorders: Evidence, Advocacy, and the Internet', Journal of Autism and Developmental Disorders, vol. 43, no. 1, pp. 122-133. https://doi.org/10.1007/s10803-012-1551-7

APA

Di Pietro, N. C., Whiteley, L. E., Mizgalewicz, A., & Illes, J. (2013). Treatments for Neurodevelopmental Disorders: Evidence, Advocacy, and the Internet. Journal of Autism and Developmental Disorders, 43(1), 122-133. https://doi.org/10.1007/s10803-012-1551-7

Vancouver

Di Pietro NC, Whiteley LE, Mizgalewicz A, Illes J. Treatments for Neurodevelopmental Disorders: Evidence, Advocacy, and the Internet. Journal of Autism and Developmental Disorders. 2013;43(1):122-133. https://doi.org/10.1007/s10803-012-1551-7

Author

Di Pietro, Nina C ; Whiteley, Louise Emma ; Mizgalewicz, Ania ; Illes, Judy. / Treatments for Neurodevelopmental Disorders : Evidence, Advocacy, and the Internet. In: Journal of Autism and Developmental Disorders. 2013 ; Vol. 43, No. 1. pp. 122-133.

Bibtex

@article{cd682935ea3f4242aa596abf09cabb6c,
title = "Treatments for Neurodevelopmental Disorders: Evidence, Advocacy, and the Internet",
abstract = "The Internet is a major source of health-related information for parents of sick children despite concerns surrounding quality. For neurodevelopmental disorders, the websites of advocacy groups are a largely unexamined source of information. We evaluated treatment information posted on nine highly-trafficked advocacy websites for autism, cerebral palsy, and fetal alcohol spectrum disorder. We found that the majority of claims about treatment safety and efficacy were unsubstantiated. Instead, a range of rhetorical strategies were used to imply scientific support. When peer-reviewed publications were cited, 20 % were incorrect or irrelevant. We call for new partnerships between advocacy and experts in developmental disorders to ensure better accuracy and higher transparency about how treatment information is selected and evidenced on advocacy websites.",
author = "{Di Pietro}, {Nina C} and Whiteley, {Louise Emma} and Ania Mizgalewicz and Judy Illes",
year = "2013",
doi = "10.1007/s10803-012-1551-7",
language = "English",
volume = "43",
pages = "122--133",
journal = "Journal of Autism and Developmental Disorders",
issn = "0162-3257",
publisher = "Springer",
number = "1",

}

RIS

TY - JOUR

T1 - Treatments for Neurodevelopmental Disorders

T2 - Evidence, Advocacy, and the Internet

AU - Di Pietro, Nina C

AU - Whiteley, Louise Emma

AU - Mizgalewicz, Ania

AU - Illes, Judy

PY - 2013

Y1 - 2013

N2 - The Internet is a major source of health-related information for parents of sick children despite concerns surrounding quality. For neurodevelopmental disorders, the websites of advocacy groups are a largely unexamined source of information. We evaluated treatment information posted on nine highly-trafficked advocacy websites for autism, cerebral palsy, and fetal alcohol spectrum disorder. We found that the majority of claims about treatment safety and efficacy were unsubstantiated. Instead, a range of rhetorical strategies were used to imply scientific support. When peer-reviewed publications were cited, 20 % were incorrect or irrelevant. We call for new partnerships between advocacy and experts in developmental disorders to ensure better accuracy and higher transparency about how treatment information is selected and evidenced on advocacy websites.

AB - The Internet is a major source of health-related information for parents of sick children despite concerns surrounding quality. For neurodevelopmental disorders, the websites of advocacy groups are a largely unexamined source of information. We evaluated treatment information posted on nine highly-trafficked advocacy websites for autism, cerebral palsy, and fetal alcohol spectrum disorder. We found that the majority of claims about treatment safety and efficacy were unsubstantiated. Instead, a range of rhetorical strategies were used to imply scientific support. When peer-reviewed publications were cited, 20 % were incorrect or irrelevant. We call for new partnerships between advocacy and experts in developmental disorders to ensure better accuracy and higher transparency about how treatment information is selected and evidenced on advocacy websites.

U2 - 10.1007/s10803-012-1551-7

DO - 10.1007/s10803-012-1551-7

M3 - Journal article

C2 - 22592952

VL - 43

SP - 122

EP - 133

JO - Journal of Autism and Developmental Disorders

JF - Journal of Autism and Developmental Disorders

SN - 0162-3257

IS - 1

ER -

ID: 40324634