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Reducing intrusive traumatic memories after emergency caesarean section: A proof-of-principle randomized controlled study

Preventative psychological interventions to aid women after traumatic childbirth are needed. This proof-of-principle randomized controlled study evaluated whether the number of intrusive traumatic memories mothers experience after emergency caesarean section (ECS) could be reduced by a brief cogniti...

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Autores principales: Horsch, Antje, Vial, Yvan, Favrod, Céline, Harari, Mathilde Morisod, Blackwell, Simon E., Watson, Peter, Iyadurai, Lalitha, Bonsall, Michael B., Holmes, Emily A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466064/
https://www.ncbi.nlm.nih.gov/pubmed/28453969
http://dx.doi.org/10.1016/j.brat.2017.03.018
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author Horsch, Antje
Vial, Yvan
Favrod, Céline
Harari, Mathilde Morisod
Blackwell, Simon E.
Watson, Peter
Iyadurai, Lalitha
Bonsall, Michael B.
Holmes, Emily A.
author_facet Horsch, Antje
Vial, Yvan
Favrod, Céline
Harari, Mathilde Morisod
Blackwell, Simon E.
Watson, Peter
Iyadurai, Lalitha
Bonsall, Michael B.
Holmes, Emily A.
author_sort Horsch, Antje
collection PubMed
description Preventative psychological interventions to aid women after traumatic childbirth are needed. This proof-of-principle randomized controlled study evaluated whether the number of intrusive traumatic memories mothers experience after emergency caesarean section (ECS) could be reduced by a brief cognitive intervention. 56 women after ECS were randomized to one of two parallel groups in a 1:1 ratio: intervention (usual care plus cognitive task procedure) or control (usual care). The intervention group engaged in a visuospatial task (computer-game ‘Tetris’ via a handheld gaming device) for 15 min within six hours following their ECS. The primary outcome was the number of intrusive traumatic memories related to the ECS recorded in a diary for the week post-ECS. As predicted, compared with controls, the intervention group reported fewer intrusive traumatic memories (M = 4.77, SD = 10.71 vs. M = 9.22, SD = 10.69, d = 0.647 [95% CI: 0.106, 1.182]) over 1 week (intention-to-treat analyses, primary outcome). There was a trend towards reduced acute stress re-experiencing symptoms (d = 0.503 [95% CI: −0.032, 1.033]) after 1 week (intention-to-treat analyses). Times series analysis on daily intrusions data confirmed the predicted difference between groups. 72% of women rated the intervention “rather” to “extremely” acceptable. This represents a first step in the development of an early (and potentially universal) intervention to prevent postnatal posttraumatic stress symptoms that may benefit both mother and child. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, www.clinicaltrials.gov, NCT02502513.
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spelling pubmed-54660642017-07-01 Reducing intrusive traumatic memories after emergency caesarean section: A proof-of-principle randomized controlled study Horsch, Antje Vial, Yvan Favrod, Céline Harari, Mathilde Morisod Blackwell, Simon E. Watson, Peter Iyadurai, Lalitha Bonsall, Michael B. Holmes, Emily A. Behav Res Ther Article Preventative psychological interventions to aid women after traumatic childbirth are needed. This proof-of-principle randomized controlled study evaluated whether the number of intrusive traumatic memories mothers experience after emergency caesarean section (ECS) could be reduced by a brief cognitive intervention. 56 women after ECS were randomized to one of two parallel groups in a 1:1 ratio: intervention (usual care plus cognitive task procedure) or control (usual care). The intervention group engaged in a visuospatial task (computer-game ‘Tetris’ via a handheld gaming device) for 15 min within six hours following their ECS. The primary outcome was the number of intrusive traumatic memories related to the ECS recorded in a diary for the week post-ECS. As predicted, compared with controls, the intervention group reported fewer intrusive traumatic memories (M = 4.77, SD = 10.71 vs. M = 9.22, SD = 10.69, d = 0.647 [95% CI: 0.106, 1.182]) over 1 week (intention-to-treat analyses, primary outcome). There was a trend towards reduced acute stress re-experiencing symptoms (d = 0.503 [95% CI: −0.032, 1.033]) after 1 week (intention-to-treat analyses). Times series analysis on daily intrusions data confirmed the predicted difference between groups. 72% of women rated the intervention “rather” to “extremely” acceptable. This represents a first step in the development of an early (and potentially universal) intervention to prevent postnatal posttraumatic stress symptoms that may benefit both mother and child. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, www.clinicaltrials.gov, NCT02502513. Elsevier Science 2017-07 /pmc/articles/PMC5466064/ /pubmed/28453969 http://dx.doi.org/10.1016/j.brat.2017.03.018 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Horsch, Antje
Vial, Yvan
Favrod, Céline
Harari, Mathilde Morisod
Blackwell, Simon E.
Watson, Peter
Iyadurai, Lalitha
Bonsall, Michael B.
Holmes, Emily A.
Reducing intrusive traumatic memories after emergency caesarean section: A proof-of-principle randomized controlled study
title Reducing intrusive traumatic memories after emergency caesarean section: A proof-of-principle randomized controlled study
title_full Reducing intrusive traumatic memories after emergency caesarean section: A proof-of-principle randomized controlled study
title_fullStr Reducing intrusive traumatic memories after emergency caesarean section: A proof-of-principle randomized controlled study
title_full_unstemmed Reducing intrusive traumatic memories after emergency caesarean section: A proof-of-principle randomized controlled study
title_short Reducing intrusive traumatic memories after emergency caesarean section: A proof-of-principle randomized controlled study
title_sort reducing intrusive traumatic memories after emergency caesarean section: a proof-of-principle randomized controlled study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466064/
https://www.ncbi.nlm.nih.gov/pubmed/28453969
http://dx.doi.org/10.1016/j.brat.2017.03.018
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