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Effectiveness of an EMDR Intervention for Perinatal Loss

Effectiveness of an Eye Movement Desensitization and Reprocessing (EMDR) Intervention for the Prevention of Post-traumatic Symptoms in Perinatal Loss

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05701137
Enrollment
40
Registered
2023-01-27
Start date
2023-04-17
Completion date
2025-03-23
Last updated
2025-07-04

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

Conditions

Pregnancy Loss, PTSD

Keywords

perinatal loss, PTSD, EMDR

Brief summary

The investigators objectives is to assess the effectiveness of Eye Movement Desensitization and Reprocessing - recent traumatic episode (EMDR-RTE) as a preventive intervention for Posttraumatic Stress Disorder (PTSD) symptoms after perinatal loss. The hypothesis is that EMDR-RTE treatment may prevent post-traumatic and depressive symptoms in women who suffered perinatal loss.

Detailed description

Perinatal loss is a general term that refers to a loss from conception to one month postpartum. It is a grief that is still socially unauthorized, however, it is a situation with significant traumatic potential. However, there are no studies evaluating the effectiveness of Eye Movement Desensitization and Reprocessing (EMDR) for the prevention or treatment of perinatal loss. We propose an one-site, open label, randomized controlled trial with the aim of assessing the effectiveness of EMDR recent traumatic episode (EMDR-RTE) as a preventive intervention for PTSD symptoms after perinatal loss. A total of 40 women who have suffered a perinatal loss from the Maternal-Fetal Medicine Service of a tertiary university hospital will be recruited. Women will be randomized to EMDR-RTE or treatment as usual (TAU). Researchers will compare EMDR-RTE and TAU to see if women receiving EMDR-RTE treatment had lower levels of post-traumatic and depressive symptoms.

Interventions

OTHEREMDR-RTE

The experimental group will have EMDR recent traumatic event.

OTHERTAU

The comparator group will have usual psychological intervention.

Sponsors

EMDR Europe
CollaboratorINDUSTRY
Hospital Clinic of Barcelona
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* be over 18 years old * agree to participate and sign the informed consent * request psychological treatment

Exclusion criteria

* active substance use disorder * cognitive disability * language barrier

Design outcomes

Primary

MeasureTime frameDescription
PCL-5Within the first month after perinatal lossPTSD Checklist for DSM-5

Secondary

MeasureTime frameDescription
STAI S/TWithin the first month after perinatal lossSpielberger State/Trait Anxiety Inventory
BDI-IIWithin the first month after perinatal lossBeck Depression Inventory

Other

MeasureTime frame
Satisfaction survey3 months after perinatal loss

Countries

Spain

Outcome results

None listed

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