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dc.contributor.authorHall, Charlotte L.
dc.contributor.authorBrown, Nikki
dc.date.accessioned2020-02-06T10:59:01Z
dc.date.available2020-02-06T10:59:01Z
dc.date.issued2020
dc.identifier.citationLennox, C., Hall, C. L., Carter, L.-A., Beresford, B., Young, S., Kraam, A., Brown, N., Wilkinson-Cunningham, L., Reeves, M. & Chitsabesan, P. (2020). FACT: a randomised controlled trial to assess the feasibility of QbTest in the assessment process of attention deficit hyperactivity disorder (ADHD) for young people in prison-a feasibility trial protocol. BMJ Open, 10 (1), pp.e035519.en
dc.identifier.other10.1136/bmjopen-2019-035519
dc.identifier.urihttp://hdl.handle.net/20.500.12904/7742
dc.description© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
dc.description.abstractINTRODUCTIONThe prevalence of attention deficit hyperactivity disorder (ADHD) within the Children and Young People Secure Estate (CYPSE) is much higher than seen in the general population. To make a diagnosis of ADHD, clinicians draw on information from multiple sources, including parents and teachers. However, obtaining these is particularly difficult for young people in the secure estate. There is increasing evidence in the community that QbTest is able to assist in the accurate and earlier diagnosis of ADHD. The objective of this study is to assess the feasibility and acceptability of QbTest in the assessment of ADHD within the CYPSE.METHODS AND ANALYSISA single-centre parallel group feasibility randomised controlled trial will be conducted. Sixty young people within the CYPSE identified as displaying possible symptoms of ADHD will be randomised to the intervention arm (n=30; QbTest plus usual care) or control arm (n=30; usual care). Primary analyses will be descriptive and a process evaluation will be conducted to assess the contexts involved in implementing the intervention. Interviews will be conducted to explore acceptability and thematic analysis will be used to analyse the data.ETHICS AND DISSEMINATIONThis study was approved by National Health Service Wales research ethics committee 3 (18/WA/0347) on 15 February 2019. The findings will be published in peer-reviewed journals, presented at relevant conferences and disseminated to the public via summaries cocreated with our patient and public involvement group.TRIAL REGISTRATION NUMBERISRCTN17402196.en
dc.description.urihttps://bmjopen.bmj.com/content/10/1/e035519en
dc.subjectChild psychiatryen
dc.subjectAttention deficit disorder with hyperactivityen
dc.subjectPrisonsen
dc.subjectOutcome assessment (Health care)en
dc.titleFACT: a randomised controlled trial to assess the feasibility of QbTest in the assessment process of attention deficit hyperactivity disorder (ADHD) for young people in prison-a feasibility trial protocolen
dc.typeArticleen
refterms.dateFOA2021-11-30T16:42:06Z


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