Key factors in children's competence to consent to clinical research
Although law is established on a strong presumption that persons younger than a certain age are not competent to consent, statutory age limits for asking children's consent to clinical research differ widely internationally. From a clinical perspective, competence is assumed to involve many fac...
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description | Although law is established on a strong presumption that persons younger than a certain age are not competent to consent, statutory age limits for asking children's consent to clinical research differ widely internationally. From a clinical perspective, competence is assumed to involve many factors including the developmental stage, the influence of parents and peers, and life experience. We examined potential determining factors for children's competence to consent to clinical research and to what extent they explain the variation in competence judgments.
From January 1, 2012 through January 1, 2014, pediatric patients aged 6 to 18 years, eligible for clinical research studies were enrolled prospectively at various in- and outpatient pediatric departments. Children's competence to consent was assessed by MacArthur Competence Assessment Tool for Clinical Research. Potential determining child variables included age, gender, intelligence, disease experience, ethnicity and socio-economic status (SES). We used logistic regression analysis and change in explained variance in competence judgments to quantify the contribution of a child variable to the total explained variance. Contextual factors included risk and complexity of the decision to participate, parental competence judgment and the child's or parents decision to participate.
Out of 209 eligible patients, 161 were included (mean age, 10.6 years, 47.2 % male). Age, SES, intelligence, ethnicity, complexity, parental competence judgment and trial participation were univariately associated with competence (P < 0.05). Total explained variance in competence judgments was 71.5 %. Only age and intelligence significantly and independently explained the variance in competence judgments, explaining 56.6 % and 12.7 % of the total variance respectively. SES, male gender, disease experience and ethnicity each explained less than 1 % of the variance in competence judgments. Contextual factors together explained an extra 2.8 % (P > 0.05).
Age is the factor that explaines most of to the variance in children's competence to consent, followed by intelligence. Experience with disease did not affect competence in this study, nor did other variables.
Development and use of a standardized instrument for assessing children's competence to consent in drug trials: Are legally established age limits valid?, NTR3918. |
doi_str_mv | 10.1186/s12910-015-0066-0 |
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From January 1, 2012 through January 1, 2014, pediatric patients aged 6 to 18 years, eligible for clinical research studies were enrolled prospectively at various in- and outpatient pediatric departments. Children's competence to consent was assessed by MacArthur Competence Assessment Tool for Clinical Research. Potential determining child variables included age, gender, intelligence, disease experience, ethnicity and socio-economic status (SES). We used logistic regression analysis and change in explained variance in competence judgments to quantify the contribution of a child variable to the total explained variance. Contextual factors included risk and complexity of the decision to participate, parental competence judgment and the child's or parents decision to participate.
Out of 209 eligible patients, 161 were included (mean age, 10.6 years, 47.2 % male). Age, SES, intelligence, ethnicity, complexity, parental competence judgment and trial participation were univariately associated with competence (P < 0.05). Total explained variance in competence judgments was 71.5 %. Only age and intelligence significantly and independently explained the variance in competence judgments, explaining 56.6 % and 12.7 % of the total variance respectively. SES, male gender, disease experience and ethnicity each explained less than 1 % of the variance in competence judgments. Contextual factors together explained an extra 2.8 % (P > 0.05).
Age is the factor that explaines most of to the variance in children's competence to consent, followed by intelligence. Experience with disease did not affect competence in this study, nor did other variables.
Development and use of a standardized instrument for assessing children's competence to consent in drug trials: Are legally established age limits valid?, NTR3918.</description><identifier>ISSN: 1472-6939</identifier><identifier>EISSN: 1472-6939</identifier><identifier>DOI: 10.1186/s12910-015-0066-0</identifier><identifier>PMID: 26498961</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adolescent ; Age Factors ; Bioethics ; Biomedical Research - ethics ; Child ; Comprehension ; Female ; Humans ; Informed Consent By Minors - ethics ; Informed Consent By Minors - legislation & jurisprudence ; Judgments ; Laws, regulations and rules ; Liability, Legal ; Male ; Mental Competency - legislation & jurisprudence ; Methods ; Parents ; Patient Selection - ethics ; Prospective Studies</subject><ispartof>BMC medical ethics, 2015-10, Vol.16 (1), p.74-74, Article 74</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Hein et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c596t-579feb09ddd0bc1ad1364b504f74d61c69d5f5a7995a7130bba08291365c742c3</citedby><cites>FETCH-LOGICAL-c596t-579feb09ddd0bc1ad1364b504f74d61c69d5f5a7995a7130bba08291365c742c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619576/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619576/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26498961$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hein, Irma M</creatorcontrib><creatorcontrib>Troost, Pieter W</creatorcontrib><creatorcontrib>Lindeboom, Robert</creatorcontrib><creatorcontrib>Benninga, Marc A</creatorcontrib><creatorcontrib>Zwaan, C Michel</creatorcontrib><creatorcontrib>van Goudoever, Johannes B</creatorcontrib><creatorcontrib>Lindauer, Ramón J L</creatorcontrib><title>Key factors in children's competence to consent to clinical research</title><title>BMC medical ethics</title><addtitle>BMC Med Ethics</addtitle><description>Although law is established on a strong presumption that persons younger than a certain age are not competent to consent, statutory age limits for asking children's consent to clinical research differ widely internationally. From a clinical perspective, competence is assumed to involve many factors including the developmental stage, the influence of parents and peers, and life experience. We examined potential determining factors for children's competence to consent to clinical research and to what extent they explain the variation in competence judgments.
From January 1, 2012 through January 1, 2014, pediatric patients aged 6 to 18 years, eligible for clinical research studies were enrolled prospectively at various in- and outpatient pediatric departments. Children's competence to consent was assessed by MacArthur Competence Assessment Tool for Clinical Research. Potential determining child variables included age, gender, intelligence, disease experience, ethnicity and socio-economic status (SES). We used logistic regression analysis and change in explained variance in competence judgments to quantify the contribution of a child variable to the total explained variance. Contextual factors included risk and complexity of the decision to participate, parental competence judgment and the child's or parents decision to participate.
Out of 209 eligible patients, 161 were included (mean age, 10.6 years, 47.2 % male). Age, SES, intelligence, ethnicity, complexity, parental competence judgment and trial participation were univariately associated with competence (P < 0.05). Total explained variance in competence judgments was 71.5 %. Only age and intelligence significantly and independently explained the variance in competence judgments, explaining 56.6 % and 12.7 % of the total variance respectively. SES, male gender, disease experience and ethnicity each explained less than 1 % of the variance in competence judgments. Contextual factors together explained an extra 2.8 % (P > 0.05).
Age is the factor that explaines most of to the variance in children's competence to consent, followed by intelligence. Experience with disease did not affect competence in this study, nor did other variables.
Development and use of a standardized instrument for assessing children's competence to consent in drug trials: Are legally established age limits valid?, NTR3918.</description><subject>Adolescent</subject><subject>Age Factors</subject><subject>Bioethics</subject><subject>Biomedical Research - ethics</subject><subject>Child</subject><subject>Comprehension</subject><subject>Female</subject><subject>Humans</subject><subject>Informed Consent By Minors - ethics</subject><subject>Informed Consent By Minors - legislation & jurisprudence</subject><subject>Judgments</subject><subject>Laws, regulations and rules</subject><subject>Liability, Legal</subject><subject>Male</subject><subject>Mental Competency - legislation & jurisprudence</subject><subject>Methods</subject><subject>Parents</subject><subject>Patient Selection - ethics</subject><subject>Prospective Studies</subject><issn>1472-6939</issn><issn>1472-6939</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>KPI</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqNkk1v1DAQhi0EoqXwA7igSByAQ4on8Ud8QaoKtKtWKuLrajnOZNdVYi92gui_x9stpYs4VJbssf28Y4_9EvIc6CFAI94mqBTQkgIvKRWipA_IPjBZlULV6uGdeI88SemSUpBNXT0me5VgqlEC9sn7M7wqemOnEFPhfGFXbugi-lepsGFc44TeYjGFPPMJ_XQdDs47a4YiYkIT7eopedSbIeGzm_GAfPv44evxaXl-cbI4PjovLVdiKrlUPbZUdV1HWwumg1qwllPWS9YJsEJ1vOdGKpU7qGnbGtrkCmvBrWSVrQ_Iu23e9dyO2Nl8n2gGvY5uNPFKB-P07o53K70MPzUToLgUOcHrmwQx_JgxTXp0yeIwGI9hThpkJVXTwDX68h_0MszR5_IyJZWkjRTNX2ppBtTO9yGfazdJ9RFnwBgHpjJ1-B8qtw5Hlx8We5fXdwRvdgSZmfDXtDRzSvrs0-Le7OLL5_uzF993WdiyNoaUIva37wxUb-ynt_bT2X56Yz9Ns-bF3Q-6VfzxW_0b4l3Q_w</recordid><startdate>20151024</startdate><enddate>20151024</enddate><creator>Hein, Irma M</creator><creator>Troost, Pieter W</creator><creator>Lindeboom, Robert</creator><creator>Benninga, Marc A</creator><creator>Zwaan, C Michel</creator><creator>van Goudoever, Johannes B</creator><creator>Lindauer, Ramón J L</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>KPI</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>AABKS</scope><scope>ABSDQ</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151024</creationdate><title>Key factors in children's competence to consent to clinical research</title><author>Hein, Irma M ; Troost, Pieter W ; Lindeboom, Robert ; Benninga, Marc A ; Zwaan, C Michel ; van Goudoever, Johannes B ; Lindauer, Ramón J L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c596t-579feb09ddd0bc1ad1364b504f74d61c69d5f5a7995a7130bba08291365c742c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Age Factors</topic><topic>Bioethics</topic><topic>Biomedical Research - ethics</topic><topic>Child</topic><topic>Comprehension</topic><topic>Female</topic><topic>Humans</topic><topic>Informed Consent By Minors - ethics</topic><topic>Informed Consent By Minors - legislation & jurisprudence</topic><topic>Judgments</topic><topic>Laws, regulations and rules</topic><topic>Liability, Legal</topic><topic>Male</topic><topic>Mental Competency - legislation & jurisprudence</topic><topic>Methods</topic><topic>Parents</topic><topic>Patient Selection - ethics</topic><topic>Prospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hein, Irma M</creatorcontrib><creatorcontrib>Troost, Pieter W</creatorcontrib><creatorcontrib>Lindeboom, Robert</creatorcontrib><creatorcontrib>Benninga, Marc A</creatorcontrib><creatorcontrib>Zwaan, C Michel</creatorcontrib><creatorcontrib>van Goudoever, Johannes B</creatorcontrib><creatorcontrib>Lindauer, Ramón J L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>Gale In Context: Global Issues</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Philosophy Collection</collection><collection>Philosophy Database</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC medical ethics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hein, Irma M</au><au>Troost, Pieter W</au><au>Lindeboom, Robert</au><au>Benninga, Marc A</au><au>Zwaan, C Michel</au><au>van Goudoever, Johannes B</au><au>Lindauer, Ramón J L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Key factors in children's competence to consent to clinical research</atitle><jtitle>BMC medical ethics</jtitle><addtitle>BMC Med Ethics</addtitle><date>2015-10-24</date><risdate>2015</risdate><volume>16</volume><issue>1</issue><spage>74</spage><epage>74</epage><pages>74-74</pages><artnum>74</artnum><issn>1472-6939</issn><eissn>1472-6939</eissn><abstract>Although law is established on a strong presumption that persons younger than a certain age are not competent to consent, statutory age limits for asking children's consent to clinical research differ widely internationally. From a clinical perspective, competence is assumed to involve many factors including the developmental stage, the influence of parents and peers, and life experience. We examined potential determining factors for children's competence to consent to clinical research and to what extent they explain the variation in competence judgments.
From January 1, 2012 through January 1, 2014, pediatric patients aged 6 to 18 years, eligible for clinical research studies were enrolled prospectively at various in- and outpatient pediatric departments. Children's competence to consent was assessed by MacArthur Competence Assessment Tool for Clinical Research. Potential determining child variables included age, gender, intelligence, disease experience, ethnicity and socio-economic status (SES). We used logistic regression analysis and change in explained variance in competence judgments to quantify the contribution of a child variable to the total explained variance. Contextual factors included risk and complexity of the decision to participate, parental competence judgment and the child's or parents decision to participate.
Out of 209 eligible patients, 161 were included (mean age, 10.6 years, 47.2 % male). Age, SES, intelligence, ethnicity, complexity, parental competence judgment and trial participation were univariately associated with competence (P < 0.05). Total explained variance in competence judgments was 71.5 %. Only age and intelligence significantly and independently explained the variance in competence judgments, explaining 56.6 % and 12.7 % of the total variance respectively. SES, male gender, disease experience and ethnicity each explained less than 1 % of the variance in competence judgments. Contextual factors together explained an extra 2.8 % (P > 0.05).
Age is the factor that explaines most of to the variance in children's competence to consent, followed by intelligence. Experience with disease did not affect competence in this study, nor did other variables.
Development and use of a standardized instrument for assessing children's competence to consent in drug trials: Are legally established age limits valid?, NTR3918.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26498961</pmid><doi>10.1186/s12910-015-0066-0</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Age Factors Bioethics Biomedical Research - ethics Child Comprehension Female Humans Informed Consent By Minors - ethics Informed Consent By Minors - legislation & jurisprudence Judgments Laws, regulations and rules Liability, Legal Male Mental Competency - legislation & jurisprudence Methods Parents Patient Selection - ethics Prospective Studies |
title | Key factors in children's competence to consent to clinical research |
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