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Study identifier: NCT04672551 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

EMDR Treatment in PTSD Following Cardiac Events

Condition: Posttraumatic Stress Disorder · Myocardial Infarction · Eye Movement Desensitization and Reprocessing  ·  Sponsor: University of Zurich

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

Cardiac events can often result in debilitating and persistent psychological symptoms. A key question involves whether optimal treatment of cardiac-induced posttraumatic stress disorder (PTSD) reduces PTSD symptoms and thereby may offset the risk of recurrent or worsening cardiovascular disease. Cardiac-induced PTSD 1) is prevalent, 2) features symptoms unique to internal ongoing somatic threat, with fears and worries that can be distinguished from PTSD resulting from external causes, 3) is persistent, 4) is associated with negative physical and emotional consequences, and 5) has not been the subject of randomized-controlled treatment trials (RCT). There is preliminary evidence suggesting that patients with cardiac-disease induced PTSD might particularly profit from EMDR. Nevertheless, this possibility has not been tested in cardiac-induced PTSD. Currently, patients with cardiac-induced PTSD are not routinely offered trauma-focused therapies, with a lack of scientific evidence likely being one major reason for this omission. If our proposed RCT shows that EMDR can be an effective treatment for patients with ACS-induced PTSD, EMDR could be routinely implemented as first-line treatment. The RCT outcomes might inform larger trials to test whether poor prognosis in terms of major adverse cardiovascular events can be improved through EMDR in patients with cardiac-induced PTSD.

This description comes directly from the study's public registry record.

Talk to the study team

Christoph Mueller-Pfeiffer, PD Dr. med.  ·  +41 44 255 52 80  ·  christoph.mueller-pfeiffer@access.uzh.ch

Mary Princip, PD Dr. phil.  ·  +41 44 255 52 80  ·  mary.princip@usz.ch

Always discuss trial participation with your own doctor first.

Locations (1)

University Hospital ZurichZurich, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT04672551