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D‐cycloserine‐augmented one‐session treatment of specific phobias in children and adolescents

BACKGROUND: D‐Cycloserine has potential to enhance exposure therapy outcomes. The current study presents a preliminary randomized, placebo‐controlled double‐blind pilot trial of DCS‐augmented one‐session treatment (OST) for youth (7–14 years) with specific phobia. A secondary aim of this pilot study...

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Autores principales: Farrell, Lara J., Waters, Allison M., Oar, Ella L., Tiralongo, Evelin, Garbharran, Vinay, Alston‐Knox, Clair, McConnell, Harry, Collings, Nigel, Zimmer‐Gembeck, Melanie, Donovan, Caroline L., Testa, Chris, Storch, Eric A., Ollendick, Thomas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991588/
https://www.ncbi.nlm.nih.gov/pubmed/30106248
http://dx.doi.org/10.1002/brb3.984
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author Farrell, Lara J.
Waters, Allison M.
Oar, Ella L.
Tiralongo, Evelin
Garbharran, Vinay
Alston‐Knox, Clair
McConnell, Harry
Collings, Nigel
Zimmer‐Gembeck, Melanie
Donovan, Caroline L.
Testa, Chris
Storch, Eric A.
Ollendick, Thomas H.
author_facet Farrell, Lara J.
Waters, Allison M.
Oar, Ella L.
Tiralongo, Evelin
Garbharran, Vinay
Alston‐Knox, Clair
McConnell, Harry
Collings, Nigel
Zimmer‐Gembeck, Melanie
Donovan, Caroline L.
Testa, Chris
Storch, Eric A.
Ollendick, Thomas H.
author_sort Farrell, Lara J.
collection PubMed
description BACKGROUND: D‐Cycloserine has potential to enhance exposure therapy outcomes. The current study presents a preliminary randomized, placebo‐controlled double‐blind pilot trial of DCS‐augmented one‐session treatment (OST) for youth (7–14 years) with specific phobia. A secondary aim of this pilot study was to explore the effects of youth age and within‐session fear reduction as potential moderators of DCS outcomes in order to generate hypotheses for a larger trial. It was hypothesized that DCS would be associated with greater improvements than placebo, that children (7–10 years) would have greater benefits than adolescents (11–14 years), and that DCS effects would be stronger for participants with the greater within‐session fear reduction during the OST. METHODS: Thirty‐five children and adolescents were randomized to either OST combined with DCS (n = 17), or OST combined with placebo (PBO; n = 18) and assessed at 1 week, 1 month, and 3 month following treatment. RESULTS: There were no significant pre‐ to post‐treatment or follow‐up benefits of DCS relative to placebo. Secondary analyses of age indicated that relative to PBO, DCS was associated with greater improvements for children (but not adolescents) on measures of severity at 1‐month follow‐up. Children in the DCS condition also showed significantly greater improvement to 1 month on global functioning relative to other groups. Conversely, adolescents had significant post‐treatment benefits in the PBO condition on symptom severity measures relative to DCS, and adolescents in the DCS condition had significantly poorer functioning at 3 months relative to all other groups. Finally, there was a trend for within‐session fear reduction to be associated with moderating effects of DCS, whereby greater reduction in fear was associated with greater functioning at one‐month follow‐up for children who received DCS, relative to PBO. LIMITATIONS: The study sample was small and therefore conclusions are tentative and require replication. CONCLUSIONS: Age and within‐session fear reduction may be important moderators of DCS‐augmented one‐session exposure therapy, which requires testing in a fully powered randomized controlled trial.
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spelling pubmed-59915882018-06-20 D‐cycloserine‐augmented one‐session treatment of specific phobias in children and adolescents Farrell, Lara J. Waters, Allison M. Oar, Ella L. Tiralongo, Evelin Garbharran, Vinay Alston‐Knox, Clair McConnell, Harry Collings, Nigel Zimmer‐Gembeck, Melanie Donovan, Caroline L. Testa, Chris Storch, Eric A. Ollendick, Thomas H. Brain Behav Original Research BACKGROUND: D‐Cycloserine has potential to enhance exposure therapy outcomes. The current study presents a preliminary randomized, placebo‐controlled double‐blind pilot trial of DCS‐augmented one‐session treatment (OST) for youth (7–14 years) with specific phobia. A secondary aim of this pilot study was to explore the effects of youth age and within‐session fear reduction as potential moderators of DCS outcomes in order to generate hypotheses for a larger trial. It was hypothesized that DCS would be associated with greater improvements than placebo, that children (7–10 years) would have greater benefits than adolescents (11–14 years), and that DCS effects would be stronger for participants with the greater within‐session fear reduction during the OST. METHODS: Thirty‐five children and adolescents were randomized to either OST combined with DCS (n = 17), or OST combined with placebo (PBO; n = 18) and assessed at 1 week, 1 month, and 3 month following treatment. RESULTS: There were no significant pre‐ to post‐treatment or follow‐up benefits of DCS relative to placebo. Secondary analyses of age indicated that relative to PBO, DCS was associated with greater improvements for children (but not adolescents) on measures of severity at 1‐month follow‐up. Children in the DCS condition also showed significantly greater improvement to 1 month on global functioning relative to other groups. Conversely, adolescents had significant post‐treatment benefits in the PBO condition on symptom severity measures relative to DCS, and adolescents in the DCS condition had significantly poorer functioning at 3 months relative to all other groups. Finally, there was a trend for within‐session fear reduction to be associated with moderating effects of DCS, whereby greater reduction in fear was associated with greater functioning at one‐month follow‐up for children who received DCS, relative to PBO. LIMITATIONS: The study sample was small and therefore conclusions are tentative and require replication. CONCLUSIONS: Age and within‐session fear reduction may be important moderators of DCS‐augmented one‐session exposure therapy, which requires testing in a fully powered randomized controlled trial. John Wiley and Sons Inc. 2018-05-01 /pmc/articles/PMC5991588/ /pubmed/30106248 http://dx.doi.org/10.1002/brb3.984 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Farrell, Lara J.
Waters, Allison M.
Oar, Ella L.
Tiralongo, Evelin
Garbharran, Vinay
Alston‐Knox, Clair
McConnell, Harry
Collings, Nigel
Zimmer‐Gembeck, Melanie
Donovan, Caroline L.
Testa, Chris
Storch, Eric A.
Ollendick, Thomas H.
D‐cycloserine‐augmented one‐session treatment of specific phobias in children and adolescents
title D‐cycloserine‐augmented one‐session treatment of specific phobias in children and adolescents
title_full D‐cycloserine‐augmented one‐session treatment of specific phobias in children and adolescents
title_fullStr D‐cycloserine‐augmented one‐session treatment of specific phobias in children and adolescents
title_full_unstemmed D‐cycloserine‐augmented one‐session treatment of specific phobias in children and adolescents
title_short D‐cycloserine‐augmented one‐session treatment of specific phobias in children and adolescents
title_sort d‐cycloserine‐augmented one‐session treatment of specific phobias in children and adolescents
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991588/
https://www.ncbi.nlm.nih.gov/pubmed/30106248
http://dx.doi.org/10.1002/brb3.984
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