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Tackling Intrusive Traumatic Memories After Childbirth

tAckling intruSive Traumatic memoRies After chiLdbirth (ASTRAL): A Single-blind Waitlist Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05381155
Acronym
ASTRAL
Enrollment
120
Registered
2022-05-19
Start date
2022-07-13
Completion date
2026-01-20
Last updated
2026-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intrusive Traumatic Memories, Posttraumatic Stress Disorder

Keywords

Posttraumatic Stress Disorder, Childbirth, Behavioral intervention, Randomized controlled trial, Visuospatial task

Brief summary

This single-blind waitlist randomized controlled trial aims to investigate the efficacy of a single-session behavioral intervention composed of a brief evocation of the childbirth memory followed by a visuospatial task (the computer game "Tetris"), on childbirth-related intrusive traumatic memories (CB-ITM) and other childbirth-related posttraumatic stress disorder (CB-PTSD) symptoms. Women who report CB-ITM after 6 weeks postpartum can be included in the study. Participants will be randomly allocated to either the immediate treatment (IT) group or to the waitlist (WL) group. Women in the IT group will first report their CB-ITM in a daily diary during 2 weeks (diary 1). On the 15th day, they will meet a psychologist to receive the single-session behavioral intervention. They will then complete a daily diary during the 2 weeks post-intervention (diary 2) and during the 5th and 6th weeks post-intervention (diary 3). Women in the WL group will report their CB-ITM continuously during 4 weeks in diary 1 and 2 before receiving the same intervention on the 30th day. They will also complete a last diary during the 2 weeks post-intervention (diary 3). It is expected that women in the immediate treatment group (IT group) will have fewer CB-ITM in diary 2, in comparison to the WL group, for which we expect no significant change in the number of CB-ITM between diary 1 and 2. This study will contribute to the development of a single-session behavioral intervention to reduce CB-ITMs and other CB-PTSD symptoms, which would reduce the distress experienced by mothers and may improve the well-being of the whole family.

Interventions

BEHAVIORALA single-session behavioral intervention composed of a brief evocation of the childbirth memory followed by a Tetris gameplay

The intervention is composed of two tasks: 1. The childbirth narration task (8-10 min.): To trigger the malleability of the traumatic childbirth memory through memory reactivation, a psychologist will ask the participants to briefly narrate their childbirth and the moment associated with their most frequent or distressing CB-ITM. This intervention part will take place on the maternity ward to use this context as a reactivation cue. 2. The visuospatial task (3 min. practice + 20 min. gameplay): Participants will be instructed to engage in a Tetris gameplay for 20 minutes on a handheld gaming device (Nintendo 3DS), which is assumed to disrupt memory reconsolidation. This part of the intervention will take place in a neutral room.

Sponsors

Centre Hospitalier Universitaire Vaudois
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

Single-blind waitlist randomized controlled trial

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Signed written consent * Gave birth in one of the study centres * Gave birth to a live baby * Had at least 4 CB-ITM over the past two weeks * Childbirth happened at least 6 weeks ago

Exclusion criteria

* Is not fluent enough in French to participate in the assessments * Life-threatening illness of mother or infant * Has an established intellectual disability or a psychotic illness * Takes propranolol medication * Alcohol and/or illicit drug abuse * Is not able to distinguish ITM linked to other traumatic events from CB-ITM targeted during the intervention * Has an ongoing psychological treatment in relation to her childbirth experience * Is under 18 years old * Being pregnant * Perinatal loss of a child born during the index traumatic childbirth

Design outcomes

Primary

MeasureTime frameDescription
The change in the number of maternal CB-ITM between the 2 weeks pre- and post-interventionDuring the 2 weeks pre- and post-interventionThe number of intrusive traumatic memories related to childbirth reported by participants in a diary during the 2 weeks pre- and post-intervention

Secondary

MeasureTime frameDescription
The change in the severity of maternal CB-PTSD symptoms between the 2nd week pre- and post-intervention2nd weeks pre- and post-interventionCity Birth Trauma Scale (CiBTS)
The change in the number of maternal CB-ITM between the 2 weeks pre-intervention, and the 5th and 6th weeks post-interventionDuring the 2 weeks pre-intervention, and the 5th and 6th weeks post-interventionThe number of intrusive traumatic memories related to childbirth reported by participants in a diary during the 2 weeks pre-intervention, and during the 5th and 6th weeks post-intervention
The change in the severity of maternal CB-PTSD symptoms between the second week pre-intervention and the 6th week post-intervention2nd week pre- and 6th week post-interventionCity Birth Trauma Scale (CiBTS)
The intervention acceptability assessed by participants from 30 to 60 days after the interventionFrom 30 to 60 days after the interventionAcceptability questionnaire specifically designed for the study

Countries

Switzerland

Contacts

PRINCIPAL_INVESTIGATORAntje Horsch, PhD

University of Lausanne and Lausanne University Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026