Show simple item record

dc.contributor.authorFarrell, L.
dc.contributor.authorWaters, A.
dc.contributor.authorBoschen, M.
dc.contributor.authorHattingh, Laetitia
dc.contributor.authorMcConnell, H.
dc.contributor.authorMilliner, E.
dc.contributor.authorCollings, N.
dc.contributor.authorZimmer-Gembeck, M.
dc.contributor.authorShelton, D.
dc.contributor.authorOllendick, T.
dc.contributor.authorTesta, C.
dc.contributor.authorStorch, E.
dc.date.accessioned2017-01-30T14:23:14Z
dc.date.available2017-01-30T14:23:14Z
dc.date.created2014-01-20T20:01:14Z
dc.date.issued2013
dc.identifier.citationFarrell, Lara J. and Waters, Allison M. and Boschen, Mark J. and Hattingh, Laetitia and McConnell, Harry and Milliner, Ella L. and Collings, Nigel and Zimmer-Gembeck, Melanie and Shelton, Doug and Ollendick, Thomas H. and Testa, Chris and Storch, Eric A. 2013. Difficult-to-treat pediatric obsessive-compulsive disorder: Feasibility and preliminary results of a randomized pilot trial of D-cycloserine-augmented behavior therapy. Depression and Anxiety. 30 (8): pp. 723-731.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/38575
dc.identifier.doi10.1002/da.22132
dc.description.abstract

Background: This study examined the feasibility and preliminary effectiveness of d-cycloserine (DCS)–augmented cognitive behavioral therapy (CBT) for children and adolescents with difficult-to-treat Obsessive Compulsive Disorder, in a double-blind randomized controlled pilot trial (RCT).Methods: Seventeen children and adolescents (aged 8–18 years) with a primary diagnosis of OCD, which was deemed difficult-to-treat, were randomly assigned to either nine sessions of CBT including five sessions of DCS-augmented exposure and response prevention (ERP) [ERP + DCS] or nine sessions of CBT including five sessions of placebo-augmented ERP [ERP + PBO]. Weight-dependent DCS or placebo doses (25 or 50 mg) were taken 1 hour before ERP sessions.Results: At post treatment, both groups showed significant improvements with 94% of the entire sample classified as responders. However, a greater improvement in the ERP + DCS relative to the ERP + PBO condition was observed at 1-month follow-up on clinician-rated obsessional severity and diagnostic severity, and parent ratings of OCD severity. There were no changes across time or condition from 1- to 3-month follow-up.Conclusions: In this preliminary study, DCS-augmented ERP produced significant improvements in OCD severity from posttreatment to 1-month follow-up, relative to a placebo control condition, in severe and difficult-to-treat pediatric OCD. The significant effect on obsessional severity suggests that DCS augmentation might be associated with enhanced modification of obsessional thoughts during ERP, and warrants further investigation.

dc.publisherWiley-Liss, Inc
dc.titleDifficult-to-treat pediatric obsessive-compulsive disorder: Feasibility and preliminary results of a randomized pilot trial of D-cycloserine-augmented behavior therapy
dc.typeJournal Article
dcterms.source.volume30
dcterms.source.startPage723
dcterms.source.endPage731
dcterms.source.issn1091-4269
dcterms.source.titleDepression and Anxiety
curtin.note

This is the accepted version of the following article: Farrell, Lara J. and Waters, Allison M. and Boschen, Mark J. and Hattingh, Laetitia et. al., 2013. Difficult-to-treat pediatric obsessive-compulsive disorder: Feasibility and preliminary results of a randomized pilot trial of D-cycloserine-augmented behavior therapy. Depression and Anxiety. 30 (8): pp. 723-731, which has been published in final form at http://doi.org/10.1002/da.22132

curtin.department
curtin.accessStatusOpen access


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record