Literature DB >> 28220724

An Observational Study of Children's Involvement in Informed Consent for Exome Sequencing Research.

Victoria A Miller1,2, Allison Werner-Lin2, Sarah A Walser2, Sawona Biswas1, Barbara A Bernhardt2.   

Abstract

The goal of this study was to examine children's involvement in consent sessions for exome sequencing research and associations of involvement with provider and parent communication. Participants included 44 children (8-17 years) from five cohorts who were offered participation in an exome sequencing study. The consent sessions were audiotaped, transcribed, and coded. Providers attempted to facilitate the child's involvement in the majority (73%) of sessions, and most (75%) children also verbally participated. Provider facilitation was strongly associated with likelihood of child participation. These findings underscore that strategies such as asking for children's opinions and soliciting their questions show respect for children and may increase the likelihood that they are engaged and involved in decisions about research participation.

Entities:  

Keywords:  assent; decision making; ethics; pediatrics; research

Mesh:

Year:  2016        PMID: 28220724      PMCID: PMC5325125          DOI: 10.1177/1556264616674096

Source DB:  PubMed          Journal:  J Empir Res Hum Res Ethics        ISSN: 1556-2646            Impact factor:   1.742


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4.  Honey, I Sequenced the Kids: Preventive Genomics and the Complexities of Adolescence.

Authors:  Maya Sabatello; Paul S Appelbaum
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5.  Patient involvement in informed consent for pediatric phase I cancer research.

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6.  Informed consent for enrolling minors in genetic susceptibility research: a qualitative study of at-risk children's and parents' views about children's role in decision-making.

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7.  A retrospective study of children's perceptions of participation as clinical research subjects in a minimal risk study.

Authors:  B S Fogas; J R Oesterheld; R I Shader
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8.  Children's competence for assent and consent: a review of empirical findings.

Authors:  Victoria A Miller; Dennis Drotar; Eric Kodish
Journal:  Ethics Behav       Date:  2004

9.  Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.

Authors:  Brooke L Levenseller; Danielle J Soucier; Victoria A Miller; Diana Harris; Laura Conway; Barbara A Bernhardt
Journal:  J Genet Couns       Date:  2013-07-12       Impact factor: 2.537

10.  Informed consent in children and adolescents: age, maturation and psychological state.

Authors:  L D Dorn; E J Susman; J C Fletcher
Journal:  J Adolesc Health       Date:  1995-03       Impact factor: 5.012

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2.  How do providers discuss the results of pediatric exome sequencing with families?

Authors:  Sarah A Walser; Allison Werner-Lin; Rebecca Mueller; Victoria A Miller; Sawona Biswas; Barbara A Bernhardt
Journal:  Per Med       Date:  2017-09-04       Impact factor: 2.512

3.  Involving Youth With a Chronic Illness in Decision-making: Highlighting the Role of Providers.

Authors:  Victoria A Miller
Journal:  Pediatrics       Date:  2018-11       Impact factor: 7.124

4.  Decisional conflict among adolescents and parents making decisions about genomic sequencing results.

Authors:  Preethi Raghuram Pillai; Cynthia A Prows; Lisa J Martin; Melanie F Myers
Journal:  Clin Genet       Date:  2019-12-02       Impact factor: 4.438

5.  Challenges to informed consent for exome sequencing: A best-worst scaling experiment.

Authors:  Rachel H Gore; John F P Bridges; Julie S Cohen; Barbara B Biesecker
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6.  A pilot study of observed physician-parent-child communication and child satisfaction in a gastroenterology clinic.

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Review 7.  Adolescent Assent and Reconsent for Biobanking: Recent Developments and Emerging Ethical Issues.

Authors:  T J Kasperbauer; Colin Halverson
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