Cost and effectiveness of one session treatment (OST) for children and young people with specific phobias compared to multi-session cognitive behavioural therapy (CBT): results from a randomised controlled trial.

Adolescent Child Cognitive behavioural therapy Cost Cost-effectiveness EQ-5D-Y Mental health services One session treatment Phobic disorders

Journal

BMC psychiatry
ISSN: 1471-244X
Titre abrégé: BMC Psychiatry
Pays: England
ID NLM: 100968559

Informations de publication

Date de publication:
12 08 2022
Historique:
received: 31 08 2021
accepted: 29 07 2022
entrez: 12 8 2022
pubmed: 13 8 2022
medline: 17 8 2022
Statut: epublish

Résumé

In the UK, around 93,000 (0.8%) children and young people (CYP) are experiencing specific phobias that have a substantial impact on daily life. The current gold-standard treatment-multi-session cognitive behavioural therapy (CBT) - is effective at reducing specific phobia severity; however, CBT is time consuming, requires specialist CBT therapists, and is often at great cost and limited availability. A briefer variant of CBT called one session treatment (OST) has been found to offer similar clinical effectiveness for specific phobia as multi-session CBT. The aim of this study was to assess the cost-effectiveness of OST compared to multi-session CBT for CYP with specific phobias through the Alleviating Specific Phobias Experienced by Children Trial (ASPECT), a two-arm, pragmatic, multi-centre, non-inferiority randomised controlled trial. CYP aged seven to 16 years with specific phobias were recruited nationally via Health and Social Care pathways, remotely randomised to the intervention group (OST) or the control group (CBT-based therapies) and analysed (n = 267). Resource use based on NHS and personal social services perspective and quality adjusted life years (QALYs) measured by EQ-5D-Y were collected at baseline and at six-month follow-up. Incremental cost-effectiveness ratio (ICER) was calculated, and non-parametric bootstrapping was conducted to capture the uncertainty around the ICER estimates. The results were presented on a cost-effectiveness acceptability curve (CEAC). A set of sensitivity analyses (including taking a societal perspective) were conducted to assess the robustness of the primary findings. After adjustment and bootstrapping, on average CYP in the OST group incurred less costs (incremental cost was -£302.96 (95% CI -£598.86 to -£28.61)) and maintained similar improvement in QALYs (QALYs gained 0.002 (95% CI - 0.004 to 0.008)). The CEAC shows that the probability of OST being cost-effective was over 95% across all the WTP thresholds. Results of a set of sensitivity analyses were consistent with the primary outcomes. Compared to CBT, OST produced a reduction in costs and maintained similar improvement in QALYs. Results from both primary and sensitivity analyses suggested that OST was highly likely to be cost saving. ISRCTN19883421 (30/11/2016).

Sections du résumé

BACKGROUND
In the UK, around 93,000 (0.8%) children and young people (CYP) are experiencing specific phobias that have a substantial impact on daily life. The current gold-standard treatment-multi-session cognitive behavioural therapy (CBT) - is effective at reducing specific phobia severity; however, CBT is time consuming, requires specialist CBT therapists, and is often at great cost and limited availability. A briefer variant of CBT called one session treatment (OST) has been found to offer similar clinical effectiveness for specific phobia as multi-session CBT. The aim of this study was to assess the cost-effectiveness of OST compared to multi-session CBT for CYP with specific phobias through the Alleviating Specific Phobias Experienced by Children Trial (ASPECT), a two-arm, pragmatic, multi-centre, non-inferiority randomised controlled trial.
METHODS
CYP aged seven to 16 years with specific phobias were recruited nationally via Health and Social Care pathways, remotely randomised to the intervention group (OST) or the control group (CBT-based therapies) and analysed (n = 267). Resource use based on NHS and personal social services perspective and quality adjusted life years (QALYs) measured by EQ-5D-Y were collected at baseline and at six-month follow-up. Incremental cost-effectiveness ratio (ICER) was calculated, and non-parametric bootstrapping was conducted to capture the uncertainty around the ICER estimates. The results were presented on a cost-effectiveness acceptability curve (CEAC). A set of sensitivity analyses (including taking a societal perspective) were conducted to assess the robustness of the primary findings.
RESULTS
After adjustment and bootstrapping, on average CYP in the OST group incurred less costs (incremental cost was -£302.96 (95% CI -£598.86 to -£28.61)) and maintained similar improvement in QALYs (QALYs gained 0.002 (95% CI - 0.004 to 0.008)). The CEAC shows that the probability of OST being cost-effective was over 95% across all the WTP thresholds. Results of a set of sensitivity analyses were consistent with the primary outcomes.
CONCLUSION
Compared to CBT, OST produced a reduction in costs and maintained similar improvement in QALYs. Results from both primary and sensitivity analyses suggested that OST was highly likely to be cost saving.
TRIAL REGISTRATION
ISRCTN19883421 (30/11/2016).

Identifiants

pubmed: 35962334
doi: 10.1186/s12888-022-04192-8
pii: 10.1186/s12888-022-04192-8
pmc: PMC9372970
doi:

Banques de données

ISRCTN
['ISRCTN19883421']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

547

Subventions

Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

© 2022. The Author(s).

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Auteurs

Han-I Wang (HI)

Department of Health Sciences, Seebohm Rowntree Building, University of York, Heslington, YO10 5DD, York, UK. han-i.wang@york.ac.uk.

Barry Wright (B)

Department of Health Sciences, Seebohm Rowntree Building, University of York, Heslington, YO10 5DD, York, UK.
Leeds and York Partnership NHS Foundation Trust, Leeds, UK.

Lucy Tindall (L)

Leeds and York Partnership NHS Foundation Trust, Leeds, UK.

Cindy Cooper (C)

University of Sheffield, Sheffield, UK.

Katie Biggs (K)

University of Sheffield, Sheffield, UK.

Ellen Lee (E)

University of Sheffield, Sheffield, UK.

M Dawn Teare (MD)

Newcastle University, Newcastle upon Tyne, UK.

Lina Gega (L)

Department of Health Sciences, Seebohm Rowntree Building, University of York, Heslington, YO10 5DD, York, UK.
Hull York Medical School, York, UK.

Alexander J Scott (AJ)

Keele University, Keele, UK.

Emily Hayward (E)

Leeds and York Partnership NHS Foundation Trust, Leeds, UK.

Kiera Solaiman (K)

University of Sheffield, Sheffield, UK.

Thompson Davis (T)

Louisiana State University, Baton Rouge, USA.
The University of Alabama, Tuscaloosa, USA.

Dean McMillan (D)

Department of Health Sciences, Seebohm Rowntree Building, University of York, Heslington, YO10 5DD, York, UK.
Hull York Medical School, York, UK.

Simon Gilbody (S)

Department of Health Sciences, Seebohm Rowntree Building, University of York, Heslington, YO10 5DD, York, UK.
Hull York Medical School, York, UK.

Steve Parrott (S)

Department of Health Sciences, Seebohm Rowntree Building, University of York, Heslington, YO10 5DD, York, UK.

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