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		<title>Big Data in Children&#8217;s Healthcare Research Wins Conditional Support from Underrepresented Groups</title>
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		<pubDate>Fri, 16 Oct 2026 19:29:09 +0000</pubDate>
				<category><![CDATA[Health]]></category>
		<category><![CDATA[Technology]]></category>
		<category><![CDATA[anonymisation]]></category>
		<category><![CDATA[big data]]></category>
		<category><![CDATA[children and young people]]></category>
		<category><![CDATA[data governance]]></category>
		<category><![CDATA[data privacy]]></category>
		<category><![CDATA[health equity]]></category>
		<category><![CDATA[informed consent]]></category>
		<category><![CDATA[medical research ethics]]></category>
		<category><![CDATA[paediatric healthcare]]></category>
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					<description><![CDATA[A systematic review of 17 studies finds that children, young people, and underserved groups support big data use in paediatric healthcare research, but only under strict conditions of anonymisation, oversight, and transparent governance.]]></description>
		
		
		
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