Clinical effectiveness of the psychological therapy Mental Health Intervention for Children with Epilepsy in addition to usual care compared with assessment-enhanced usual care alone: a multicentre, randomised controlled clinical trial in the UK

Mental health difficulties are common in children and young people with chronic health conditions, but many of those in need do not access evidence-based psychological treatments. The study aim was to evaluate the clinical effectiveness of integrated mental health treatment for children and young pe...

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Veröffentlicht in:The Lancet (British edition) 2024-03, Vol.403 (10433), p.1254-1266
Hauptverfasser: Bennett, Sophie D, Cross, J Helen, Chowdhury, Kashfia, Ford, Tamsin, Heyman, Isobel, Coughtrey, Anna E, Dalrymple, Emma, Byford, Sarah, Chorpita, Bruce, Fonagy, Peter, Moss-Morris, Rona, Reilly, Colin, Smith, Jonathan A, Stephenson, Terence, Varadkar, Sophia, Blackstone, James, Quartly, Harriet, Hughes, Tyler, Lewins, Amy, Moore, Elana, Walji, Fahreen, Welch, Alice, Whelan, Emily, Zacharia, Alice, D'Oelsnitz, Anaïs, Shah, Mariam, Xu, Laila, Vezyroglou, Aikaterini, Mitchell, Kirsten, Nizza, Isabella E, Ganguli, Poushali, Shafran, Roz
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container_issue 10433
container_start_page 1254
container_title The Lancet (British edition)
container_volume 403
creator Bennett, Sophie D
Cross, J Helen
Chowdhury, Kashfia
Ford, Tamsin
Heyman, Isobel
Coughtrey, Anna E
Dalrymple, Emma
Byford, Sarah
Chorpita, Bruce
Fonagy, Peter
Moss-Morris, Rona
Reilly, Colin
Smith, Jonathan A
Stephenson, Terence
Varadkar, Sophia
Blackstone, James
Quartly, Harriet
Hughes, Tyler
Lewins, Amy
Moore, Elana
Walji, Fahreen
Welch, Alice
Whelan, Emily
Zacharia, Alice
D'Oelsnitz, Anaïs
Shah, Mariam
Xu, Laila
Vezyroglou, Aikaterini
Mitchell, Kirsten
Nizza, Isabella E
Ganguli, Poushali
Shafran, Roz
description Mental health difficulties are common in children and young people with chronic health conditions, but many of those in need do not access evidence-based psychological treatments. The study aim was to evaluate the clinical effectiveness of integrated mental health treatment for children and young people with epilepsy, a common chronic health condition known to be associated with a particularly high rate of co-occurring mental health difficulties. We conducted a parallel group, multicentre, open-label, randomised controlled trial of participants aged 3–18 years, attending epilepsy clinics across England and Northern Ireland who met diagnostic criteria for a common mental health disorder. Participants were randomised (1:1; using an independent web-based system) to receive the Mental Health Intervention for Children with Epilepsy (MICE) in addition to usual care, or assessment-enhanced usual care alone (control). Children and young people in both groups received a full diagnostic mental health assessment. MICE was a modular psychological intervention designed to treat common mental health conditions in children and young people using evidence-based approaches such as cognitive behaviour therapy and behavioural parenting strategies. Usual care for mental health disorders varied by site but typically included referral to appropriate services. Participants, along with their caregivers, and clinicians were not masked to treatment allocation but statisticians were masked until the point of analysis. The primary outcome, analysed by modified intention-to-treat, was the parent-report Strengths and Difficulties Questionnaire (SDQ) at 6 months post-randomisation. The study is complete and registered with ISRCTN (57823197). 1401 young people were potentially deemed eligible for study inclusion. Following the exclusion of 531 young people, 870 participants were assessed for eligibility and completed the SDQ, and 480 caregivers provided consent for study inclusion between May 20, 2019, and Jan 31, 2022. Between Aug 28, 2019, and Feb 21, 2022, 334 participants (mean ages 10·5 years [SD 3·6] in the MICE group vs 10·3 [4·0] in control group at baseline) were randomly assigned to an intervention using minimisation balanced by age, primary mental health disorder, diagnosis of intellectual disability, and autistic spectrum disorder at baseline. 168 (50%) of the participants were female and 166 (50%) were male. 166 participants were randomly assigned to the MICE group and 168 w
doi_str_mv 10.1016/S0140-6736(23)02791-5
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The study aim was to evaluate the clinical effectiveness of integrated mental health treatment for children and young people with epilepsy, a common chronic health condition known to be associated with a particularly high rate of co-occurring mental health difficulties. We conducted a parallel group, multicentre, open-label, randomised controlled trial of participants aged 3–18 years, attending epilepsy clinics across England and Northern Ireland who met diagnostic criteria for a common mental health disorder. Participants were randomised (1:1; using an independent web-based system) to receive the Mental Health Intervention for Children with Epilepsy (MICE) in addition to usual care, or assessment-enhanced usual care alone (control). Children and young people in both groups received a full diagnostic mental health assessment. MICE was a modular psychological intervention designed to treat common mental health conditions in children and young people using evidence-based approaches such as cognitive behaviour therapy and behavioural parenting strategies. Usual care for mental health disorders varied by site but typically included referral to appropriate services. Participants, along with their caregivers, and clinicians were not masked to treatment allocation but statisticians were masked until the point of analysis. The primary outcome, analysed by modified intention-to-treat, was the parent-report Strengths and Difficulties Questionnaire (SDQ) at 6 months post-randomisation. The study is complete and registered with ISRCTN (57823197). 1401 young people were potentially deemed eligible for study inclusion. Following the exclusion of 531 young people, 870 participants were assessed for eligibility and completed the SDQ, and 480 caregivers provided consent for study inclusion between May 20, 2019, and Jan 31, 2022. Between Aug 28, 2019, and Feb 21, 2022, 334 participants (mean ages 10·5 years [SD 3·6] in the MICE group vs 10·3 [4·0] in control group at baseline) were randomly assigned to an intervention using minimisation balanced by age, primary mental health disorder, diagnosis of intellectual disability, and autistic spectrum disorder at baseline. 168 (50%) of the participants were female and 166 (50%) were male. 166 participants were randomly assigned to the MICE group and 168 were randomly assigned to the control group. At 6 months, the mean SDQ difficulties for the 148 participants in the MICE group was 17·6 (SD 6·3) and 19·6 (6·1) for the 148 participants in the control group. The adjusted effect of MICE was –1·7 (95% CI –2·8 to –0·5; p=0·0040; Cohen's d, 0·3). 14 (8%) patients in the MICE group experienced at least one serious adverse event compared with 24 (14%) in the control group. 68% percent of serious adverse events (50 events) were admission due to seizures. MICE was superior to assessment-enhanced usual care in improving symptoms of emotional and behavioural difficulties in young people with epilepsy and common mental health disorders. The trial therefore shows that mental health comorbidities can be effectively and safely treated by a variety of clinicians, utilising an integrated intervention across ages and in the context of intellectual disability and autism. The evidence from this trial suggests that such a model should be fully embedded in epilepsy services and serves as a model for other chronic health conditions in young people. 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Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license</rights><rights>Copyright © 2024 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.</rights><rights>2024. The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. This work is published under https://creativecommons.org/licenses/by/3.0/ (theLicense”). 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The study aim was to evaluate the clinical effectiveness of integrated mental health treatment for children and young people with epilepsy, a common chronic health condition known to be associated with a particularly high rate of co-occurring mental health difficulties. We conducted a parallel group, multicentre, open-label, randomised controlled trial of participants aged 3–18 years, attending epilepsy clinics across England and Northern Ireland who met diagnostic criteria for a common mental health disorder. Participants were randomised (1:1; using an independent web-based system) to receive the Mental Health Intervention for Children with Epilepsy (MICE) in addition to usual care, or assessment-enhanced usual care alone (control). Children and young people in both groups received a full diagnostic mental health assessment. MICE was a modular psychological intervention designed to treat common mental health conditions in children and young people using evidence-based approaches such as cognitive behaviour therapy and behavioural parenting strategies. Usual care for mental health disorders varied by site but typically included referral to appropriate services. Participants, along with their caregivers, and clinicians were not masked to treatment allocation but statisticians were masked until the point of analysis. The primary outcome, analysed by modified intention-to-treat, was the parent-report Strengths and Difficulties Questionnaire (SDQ) at 6 months post-randomisation. The study is complete and registered with ISRCTN (57823197). 1401 young people were potentially deemed eligible for study inclusion. Following the exclusion of 531 young people, 870 participants were assessed for eligibility and completed the SDQ, and 480 caregivers provided consent for study inclusion between May 20, 2019, and Jan 31, 2022. Between Aug 28, 2019, and Feb 21, 2022, 334 participants (mean ages 10·5 years [SD 3·6] in the MICE group vs 10·3 [4·0] in control group at baseline) were randomly assigned to an intervention using minimisation balanced by age, primary mental health disorder, diagnosis of intellectual disability, and autistic spectrum disorder at baseline. 168 (50%) of the participants were female and 166 (50%) were male. 166 participants were randomly assigned to the MICE group and 168 were randomly assigned to the control group. At 6 months, the mean SDQ difficulties for the 148 participants in the MICE group was 17·6 (SD 6·3) and 19·6 (6·1) for the 148 participants in the control group. The adjusted effect of MICE was –1·7 (95% CI –2·8 to –0·5; p=0·0040; Cohen's d, 0·3). 14 (8%) patients in the MICE group experienced at least one serious adverse event compared with 24 (14%) in the control group. 68% percent of serious adverse events (50 events) were admission due to seizures. MICE was superior to assessment-enhanced usual care in improving symptoms of emotional and behavioural difficulties in young people with epilepsy and common mental health disorders. The trial therefore shows that mental health comorbidities can be effectively and safely treated by a variety of clinicians, utilising an integrated intervention across ages and in the context of intellectual disability and autism. The evidence from this trial suggests that such a model should be fully embedded in epilepsy services and serves as a model for other chronic health conditions in young people. UK National Institute for Health Research Programme Grants for Applied Research programme and Epilepsy Research UK Endeavour Project Grant.</description><subject>Adolescent</subject><subject>Adverse events</subject><subject>Anxiety</subject><subject>Autism</subject><subject>Behavior therapy</subject><subject>Caregivers</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Children &amp; youth</subject><subject>Chronic illnesses</subject><subject>Clinics</subject><subject>Cognitive ability</subject><subject>Comorbidity</subject><subject>Consent</subject><subject>Cost-Benefit Analysis</subject><subject>Diagnostic systems</subject><subject>Disorders</subject><subject>Effectiveness</subject><subject>Emotional behavior</subject><subject>England</subject><subject>Epilepsy</subject><subject>Epilepsy - therapy</subject><subject>Families &amp; family life</subject><subject>Female</subject><subject>Health care</subject><subject>Health promotion</subject><subject>Humans</subject><subject>Intellectual disabilities</subject><subject>Intellectual Disability</subject><subject>Intervention</subject><subject>Male</subject><subject>Mental depression</subject><subject>Mental disorders</subject><subject>Mental Health</subject><subject>Modular design</subject><subject>Neurosciences</subject><subject>Psychosocial Intervention</subject><subject>Randomization</subject><subject>Seizures</subject><subject>Signs and symptoms</subject><subject>Treatment Outcome</subject><subject>Young 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effectiveness of the psychological therapy Mental Health Intervention for Children with Epilepsy in addition to usual care compared with assessment-enhanced usual care alone: a multicentre, randomised controlled clinical trial in the UK</title><author>Bennett, Sophie D ; Cross, J Helen ; Chowdhury, Kashfia ; Ford, Tamsin ; Heyman, Isobel ; Coughtrey, Anna E ; Dalrymple, Emma ; Byford, Sarah ; Chorpita, Bruce ; Fonagy, Peter ; Moss-Morris, Rona ; Reilly, Colin ; Smith, Jonathan A ; Stephenson, Terence ; Varadkar, Sophia ; Blackstone, James ; Quartly, Harriet ; Hughes, Tyler ; Lewins, Amy ; Moore, Elana ; Walji, Fahreen ; Welch, Alice ; Whelan, Emily ; Zacharia, Alice ; D'Oelsnitz, Anaïs ; Shah, Mariam ; Xu, Laila ; Vezyroglou, Aikaterini ; Mitchell, Kirsten ; Nizza, Isabella E ; Ganguli, Poushali ; Shafran, Roz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-fb77fe037273ecc4cbb94692880fd35409c69e39458b4ad7e53155dc4584a3453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adolescent</topic><topic>Adverse events</topic><topic>Anxiety</topic><topic>Autism</topic><topic>Behavior therapy</topic><topic>Caregivers</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Children &amp; youth</topic><topic>Chronic illnesses</topic><topic>Clinics</topic><topic>Cognitive ability</topic><topic>Comorbidity</topic><topic>Consent</topic><topic>Cost-Benefit Analysis</topic><topic>Diagnostic systems</topic><topic>Disorders</topic><topic>Effectiveness</topic><topic>Emotional behavior</topic><topic>England</topic><topic>Epilepsy</topic><topic>Epilepsy - therapy</topic><topic>Families &amp; family life</topic><topic>Female</topic><topic>Health care</topic><topic>Health promotion</topic><topic>Humans</topic><topic>Intellectual disabilities</topic><topic>Intellectual Disability</topic><topic>Intervention</topic><topic>Male</topic><topic>Mental depression</topic><topic>Mental disorders</topic><topic>Mental Health</topic><topic>Modular design</topic><topic>Neurosciences</topic><topic>Psychosocial Intervention</topic><topic>Randomization</topic><topic>Seizures</topic><topic>Signs and symptoms</topic><topic>Treatment Outcome</topic><topic>Young adults</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bennett, Sophie D</creatorcontrib><creatorcontrib>Cross, J Helen</creatorcontrib><creatorcontrib>Chowdhury, Kashfia</creatorcontrib><creatorcontrib>Ford, Tamsin</creatorcontrib><creatorcontrib>Heyman, Isobel</creatorcontrib><creatorcontrib>Coughtrey, Anna E</creatorcontrib><creatorcontrib>Dalrymple, Emma</creatorcontrib><creatorcontrib>Byford, Sarah</creatorcontrib><creatorcontrib>Chorpita, Bruce</creatorcontrib><creatorcontrib>Fonagy, Peter</creatorcontrib><creatorcontrib>Moss-Morris, Rona</creatorcontrib><creatorcontrib>Reilly, Colin</creatorcontrib><creatorcontrib>Smith, Jonathan A</creatorcontrib><creatorcontrib>Stephenson, Terence</creatorcontrib><creatorcontrib>Varadkar, Sophia</creatorcontrib><creatorcontrib>Blackstone, James</creatorcontrib><creatorcontrib>Quartly, Harriet</creatorcontrib><creatorcontrib>Hughes, Tyler</creatorcontrib><creatorcontrib>Lewins, Amy</creatorcontrib><creatorcontrib>Moore, Elana</creatorcontrib><creatorcontrib>Walji, Fahreen</creatorcontrib><creatorcontrib>Welch, Alice</creatorcontrib><creatorcontrib>Whelan, Emily</creatorcontrib><creatorcontrib>Zacharia, Alice</creatorcontrib><creatorcontrib>D'Oelsnitz, Anaïs</creatorcontrib><creatorcontrib>Shah, Mariam</creatorcontrib><creatorcontrib>Xu, Laila</creatorcontrib><creatorcontrib>Vezyroglou, Aikaterini</creatorcontrib><creatorcontrib>Mitchell, Kirsten</creatorcontrib><creatorcontrib>Nizza, Isabella E</creatorcontrib><creatorcontrib>Ganguli, Poushali</creatorcontrib><creatorcontrib>Shafran, Roz</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>News PRO</collection><collection>Pharma and Biotech Premium PRO</collection><collection>Global News &amp; ABI/Inform Professional</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS 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(Corporate)</collection><collection>Nursing &amp; Allied Health Premium</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>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>The Lancet (British edition)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bennett, Sophie D</au><au>Cross, J Helen</au><au>Chowdhury, Kashfia</au><au>Ford, Tamsin</au><au>Heyman, Isobel</au><au>Coughtrey, Anna E</au><au>Dalrymple, Emma</au><au>Byford, Sarah</au><au>Chorpita, Bruce</au><au>Fonagy, Peter</au><au>Moss-Morris, Rona</au><au>Reilly, Colin</au><au>Smith, Jonathan A</au><au>Stephenson, Terence</au><au>Varadkar, Sophia</au><au>Blackstone, James</au><au>Quartly, Harriet</au><au>Hughes, Tyler</au><au>Lewins, Amy</au><au>Moore, Elana</au><au>Walji, Fahreen</au><au>Welch, Alice</au><au>Whelan, Emily</au><au>Zacharia, Alice</au><au>D'Oelsnitz, Anaïs</au><au>Shah, Mariam</au><au>Xu, Laila</au><au>Vezyroglou, Aikaterini</au><au>Mitchell, Kirsten</au><au>Nizza, Isabella E</au><au>Ganguli, Poushali</au><au>Shafran, Roz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical effectiveness of the psychological therapy Mental Health Intervention for Children with Epilepsy in addition to usual care compared with assessment-enhanced usual care alone: a multicentre, randomised controlled clinical trial in the UK</atitle><jtitle>The Lancet (British edition)</jtitle><addtitle>Lancet</addtitle><date>2024-03-30</date><risdate>2024</risdate><volume>403</volume><issue>10433</issue><spage>1254</spage><epage>1266</epage><pages>1254-1266</pages><issn>0140-6736</issn><issn>1474-547X</issn><eissn>1474-547X</eissn><abstract>Mental health difficulties are common in children and young people with chronic health conditions, but many of those in need do not access evidence-based psychological treatments. The study aim was to evaluate the clinical effectiveness of integrated mental health treatment for children and young people with epilepsy, a common chronic health condition known to be associated with a particularly high rate of co-occurring mental health difficulties. We conducted a parallel group, multicentre, open-label, randomised controlled trial of participants aged 3–18 years, attending epilepsy clinics across England and Northern Ireland who met diagnostic criteria for a common mental health disorder. Participants were randomised (1:1; using an independent web-based system) to receive the Mental Health Intervention for Children with Epilepsy (MICE) in addition to usual care, or assessment-enhanced usual care alone (control). Children and young people in both groups received a full diagnostic mental health assessment. MICE was a modular psychological intervention designed to treat common mental health conditions in children and young people using evidence-based approaches such as cognitive behaviour therapy and behavioural parenting strategies. Usual care for mental health disorders varied by site but typically included referral to appropriate services. Participants, along with their caregivers, and clinicians were not masked to treatment allocation but statisticians were masked until the point of analysis. The primary outcome, analysed by modified intention-to-treat, was the parent-report Strengths and Difficulties Questionnaire (SDQ) at 6 months post-randomisation. The study is complete and registered with ISRCTN (57823197). 1401 young people were potentially deemed eligible for study inclusion. Following the exclusion of 531 young people, 870 participants were assessed for eligibility and completed the SDQ, and 480 caregivers provided consent for study inclusion between May 20, 2019, and Jan 31, 2022. Between Aug 28, 2019, and Feb 21, 2022, 334 participants (mean ages 10·5 years [SD 3·6] in the MICE group vs 10·3 [4·0] in control group at baseline) were randomly assigned to an intervention using minimisation balanced by age, primary mental health disorder, diagnosis of intellectual disability, and autistic spectrum disorder at baseline. 168 (50%) of the participants were female and 166 (50%) were male. 166 participants were randomly assigned to the MICE group and 168 were randomly assigned to the control group. At 6 months, the mean SDQ difficulties for the 148 participants in the MICE group was 17·6 (SD 6·3) and 19·6 (6·1) for the 148 participants in the control group. The adjusted effect of MICE was –1·7 (95% CI –2·8 to –0·5; p=0·0040; Cohen's d, 0·3). 14 (8%) patients in the MICE group experienced at least one serious adverse event compared with 24 (14%) in the control group. 68% percent of serious adverse events (50 events) were admission due to seizures. MICE was superior to assessment-enhanced usual care in improving symptoms of emotional and behavioural difficulties in young people with epilepsy and common mental health disorders. The trial therefore shows that mental health comorbidities can be effectively and safely treated by a variety of clinicians, utilising an integrated intervention across ages and in the context of intellectual disability and autism. The evidence from this trial suggests that such a model should be fully embedded in epilepsy services and serves as a model for other chronic health conditions in young people. UK National Institute for Health Research Programme Grants for Applied Research programme and Epilepsy Research UK Endeavour Project Grant.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>38461840</pmid><doi>10.1016/S0140-6736(23)02791-5</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0140-6736
ispartof The Lancet (British edition), 2024-03, Vol.403 (10433), p.1254-1266
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Adolescent
Adverse events
Anxiety
Autism
Behavior therapy
Caregivers
Child
Child, Preschool
Children
Children & youth
Chronic illnesses
Clinics
Cognitive ability
Comorbidity
Consent
Cost-Benefit Analysis
Diagnostic systems
Disorders
Effectiveness
Emotional behavior
England
Epilepsy
Epilepsy - therapy
Families & family life
Female
Health care
Health promotion
Humans
Intellectual disabilities
Intellectual Disability
Intervention
Male
Mental depression
Mental disorders
Mental Health
Modular design
Neurosciences
Psychosocial Intervention
Randomization
Seizures
Signs and symptoms
Treatment Outcome
Young adults
title Clinical effectiveness of the psychological therapy Mental Health Intervention for Children with Epilepsy in addition to usual care compared with assessment-enhanced usual care alone: a multicentre, randomised controlled clinical trial in the UK
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