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Single-session visuospatial task procedure to prevent childbirth-related posttraumatic stress disorder: a multicentre double-blind randomised controlled trial

Single-session visuospatial task procedure to prevent childbirth-related posttraumatic stress disorder: a multicentre double-blind randomised controlled trial
Single-session visuospatial task procedure to prevent childbirth-related posttraumatic stress disorder: a multicentre double-blind randomised controlled trial
Preventive evidence-based interventions for childbirth-related posttraumatic stress disorder (CB-PTSD) are lacking. Yet, 18.5% of women develop CB-PTSD symptoms following an unplanned caesarean section (UCS). This two-arm, multicentre, double-blind superiority trial tested the efficacy of an early single-session intervention including a visuospatial task on the prevention of maternal CB-PTSD symptoms. The intervention was delivered by trained maternity clinicians. Shortly after UCS, women were included if they gave birth to a live baby, provided consent, and perceived their childbirth as traumatic. Participants were randomly assigned to the intervention or attention-placebo group (allocation ratio 1:1). Assessments were done at birth, six weeks, and six months postpartum. Group differences in maternal CB-PTSD symptoms at six weeks (primary outcomes) and six months postpartum (secondary outcomes) were assessed with the self-report PTSD Checklist for DSM-5 (PCL-5) and by blinded research assessors with the Clinician-administered PTSD scale for DSM-5 (CAPS-5). Analysis was by intention-to-treat. The trial was prospectively registered (ClinicalTrials.gov, NCT03576586). Of the 2068 women assessed for eligibility, 166 were eligible and 146 were randomly assigned to the intervention (n = 74) or attention-placebo control group (n = 72). For the PCL-5, at six weeks, a marginally significant intervention effect was found on the total PCL-5 PTSD symptom count (β = −0.43, S.E. = 0.23, z = −1.88, p < 0.06), and on the intrusions (β = −0.73, S.E. = 0.38, z = −1.94, p < 0.0525) and arousal (β = −0.55, S.E. = 0.29, z = −1.92, p < 0.0552) clusters. At six months, a significant intervention effect on the total PCL-5 PTSD symptom count (β = −0.65, S.E. = 0.32, z = −2.04, p = 0.041, 95%CI[−1.27, −0.03]), on alterations in cognition and mood (β = −0.85, S.E. = 0.27, z = −3.15, p = 0.0016) and arousal (β = −0.56, S.E. = 0.26, z = −2.19, p < 0.0289, 95%CI[−1.07, −0.06]) clusters appeared. No group differences on the CAPS-5 emerged. Results provide evidence that this brief, single-session intervention carried out by trained clinicians can prevent the development of CB-PTSD symptoms up to six months postpartum.
1359-4184
3842–3850
Deforges, Camille
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Sandoz, Vania
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Noël, Yvonnick
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Avignon, Valérie
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Desseauve, David
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Bourdin, Julie
a6d017e0-fe4a-42ea-8f7f-fae1908e5fd6
Vial, Yvan
3614d0d8-18b3-4dc6-bb39-68c3b95044df
Ayers, Susan
ce36519d-3127-466a-a4a1-ade104314fd4
Holmes, Emily A.
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Epiney, Manuella
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Horsch, Antje
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Deforges, Camille
7612e261-8d5a-40a6-a163-7921b25ce96d
Sandoz, Vania
914c9261-5060-4f5c-a9e7-40efa655c813
Noël, Yvonnick
ba47913c-e946-4387-8269-d6db2dd67127
Avignon, Valérie
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Desseauve, David
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Bourdin, Julie
a6d017e0-fe4a-42ea-8f7f-fae1908e5fd6
Vial, Yvan
3614d0d8-18b3-4dc6-bb39-68c3b95044df
Ayers, Susan
ce36519d-3127-466a-a4a1-ade104314fd4
Holmes, Emily A.
a6379ab3-b182-45f8-87c9-3e07e90fe469
Epiney, Manuella
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Horsch, Antje
d9d4960f-dadf-4d64-bb16-6814916803a5

Deforges, Camille, Sandoz, Vania, Noël, Yvonnick, Avignon, Valérie, Desseauve, David, Bourdin, Julie, Vial, Yvan, Ayers, Susan, Holmes, Emily A., Epiney, Manuella and Horsch, Antje (2023) Single-session visuospatial task procedure to prevent childbirth-related posttraumatic stress disorder: a multicentre double-blind randomised controlled trial. Molecular Psychiatry, 28, 3842–3850. (doi:10.1038/s41380-023-02275-w).

Record type: Article

Abstract

Preventive evidence-based interventions for childbirth-related posttraumatic stress disorder (CB-PTSD) are lacking. Yet, 18.5% of women develop CB-PTSD symptoms following an unplanned caesarean section (UCS). This two-arm, multicentre, double-blind superiority trial tested the efficacy of an early single-session intervention including a visuospatial task on the prevention of maternal CB-PTSD symptoms. The intervention was delivered by trained maternity clinicians. Shortly after UCS, women were included if they gave birth to a live baby, provided consent, and perceived their childbirth as traumatic. Participants were randomly assigned to the intervention or attention-placebo group (allocation ratio 1:1). Assessments were done at birth, six weeks, and six months postpartum. Group differences in maternal CB-PTSD symptoms at six weeks (primary outcomes) and six months postpartum (secondary outcomes) were assessed with the self-report PTSD Checklist for DSM-5 (PCL-5) and by blinded research assessors with the Clinician-administered PTSD scale for DSM-5 (CAPS-5). Analysis was by intention-to-treat. The trial was prospectively registered (ClinicalTrials.gov, NCT03576586). Of the 2068 women assessed for eligibility, 166 were eligible and 146 were randomly assigned to the intervention (n = 74) or attention-placebo control group (n = 72). For the PCL-5, at six weeks, a marginally significant intervention effect was found on the total PCL-5 PTSD symptom count (β = −0.43, S.E. = 0.23, z = −1.88, p < 0.06), and on the intrusions (β = −0.73, S.E. = 0.38, z = −1.94, p < 0.0525) and arousal (β = −0.55, S.E. = 0.29, z = −1.92, p < 0.0552) clusters. At six months, a significant intervention effect on the total PCL-5 PTSD symptom count (β = −0.65, S.E. = 0.32, z = −2.04, p = 0.041, 95%CI[−1.27, −0.03]), on alterations in cognition and mood (β = −0.85, S.E. = 0.27, z = −3.15, p = 0.0016) and arousal (β = −0.56, S.E. = 0.26, z = −2.19, p < 0.0289, 95%CI[−1.07, −0.06]) clusters appeared. No group differences on the CAPS-5 emerged. Results provide evidence that this brief, single-session intervention carried out by trained clinicians can prevent the development of CB-PTSD symptoms up to six months postpartum.

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e-pub ahead of print date: 27 September 2023

Identifiers

Local EPrints ID: 507830
URI: http://eprints.soton.ac.uk/id/eprint/507830
ISSN: 1359-4184
PURE UUID: 2c0bd8d6-dd26-45dc-a77b-944cc3b023eb
ORCID for Emily A. Holmes: ORCID iD orcid.org/0000-0001-7319-3112

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Date deposited: 06 Jan 2026 18:02
Last modified: 08 Jan 2026 03:28

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Contributors

Author: Camille Deforges
Author: Vania Sandoz
Author: Yvonnick Noël
Author: Valérie Avignon
Author: David Desseauve
Author: Julie Bourdin
Author: Yvan Vial
Author: Susan Ayers
Author: Emily A. Holmes ORCID iD
Author: Manuella Epiney
Author: Antje Horsch

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