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Tackling Intrusive Traumatic Memories After a Difficult Birth

Tackling Intrusive Traumatic Memories After a Difficult Birth: a proof-of Principle Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04286724
Enrollment
23
Registered
2020-02-27
Start date
2020-07-08
Completion date
2021-04-14
Last updated
2021-06-22

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

Brief summary

This proof-of-principle study aims to investigate the effects of a brief behavioural procedure including a computerized visuospatial task (the computer game Tetris) preceded by a reactivation of the traumatic memory of childbirth, on birth-related intrusive traumatic memories and other postpartum posttraumatic stress symptoms. Women who report birth-related intrusive memories after 6 weeks postpartum will monitor their intrusive traumatic memories in a daily diary. After two weeks of diary, they will meet a psychologist to briefly evoke the memory of their birth, and receive a brief behavioural procedure including playing Tetris. Participants will then continue to complete an intrusive traumatic memory diary during two weeks. It is predicted that they will report fewer intrusive memories in the two weeks following the intervention, compared to the two weeks before. This will inform the potential future development of a simple computerized intervention procedure to reduce distressing psychological symptoms after traumatic childbirth.

Interventions

BEHAVIORALBrief behavioural procedure including a computerized visuospatial task (computer game Tetris)

Brief behavioural procedure including a computerized visuospatial task (the computer game Tetris) preceded by a reactivation of the traumatic memory of childbirth

Sponsors

Antje Horsch
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Single group pre-post study

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Gave birth at the Lausanne University Hospital * Gave written consent * Have at least 4 related-to-childbirth intrusions over the two weeks prior to recruitment, and at least 2 related-to-childbirth intrusions during the pre-intervention diary * Gave birth more than 6 weeks ago * Is able to distinguish intrusions linked to the traumatic childbirth from intrusions linked to other traumatic events

Exclusion criteria

* Gave birth to a stillborn child * Not fluent in French * Severe illness of mother or infant (e.g. cancer, cardiovascular disease, severe neurodevelopmental difficulties, malformations) * Have an established intellectual disability, or psychiatric history such as psychotic illness * Alcohol abuse and/or illegal drug use * Currently receiving psychological care in relation with the traumatic birth experience

Design outcomes

Primary

MeasureTime frameDescription
Frequency of intrusive memories of the index traumaWithin 2 weeks following the interventionFrequency of intrusive traumatic memories related to childbirth recorded by participants in a trauma-related intrusive memories diary over the two weeks after the intervention

Secondary

MeasureTime frameDescription
Presence and severity of maternal PTSD symptoms1 month after the interventionPTSD Checklist (PCL-5) for DSM-5
Frequency of intrusive memories of the index traumaBetween 4 and 6 weeks after the interventionFrequency of intrusive traumatic memories related to childbirth recorded by participants in a trauma-related intrusive memories diary between the 4th and 6th weeks following the intervention
Psychological distress related to intrusive memories of the index traumaWithin 2 weeks following the interventionRating scale for psychological distress related to intrusive memories related to childbirth that are reported in an intrusive memories diary over the two weeks after the intervention. It is a SUDS (Subjective Units of Distress Scale) from 1 to 10 (1= No distress at all while having the intrusion ; 10 = Extreme distress while having the intrusion).

Other

MeasureTime frameDescription
Intervention acceptability1 month after the intervention10-point Likert scale (1= The intervention was not at all acceptable; 10 = The intervention was extremely acceptable).

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026