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Clinical Trials in Switzerland / NCT04672551
Recruiting Not applicable

EMDR Treatment in PTSD Following Cardiac Events

NCT04672551 · tracked via the Priya Life Science Switzerland tracker
Phase
Not applicable
Started
2020-11-21
Last updated
2026-05-07

Condition(s) studied

Posttraumatic Stress DisorderMyocardial InfarctionEye Movement Desensitization and Reprocessing

Investigational drug(s) / intervention(s)

EMDR Treatment

EMDR Treatment: Eight individual EMDR sessions lasting for 1 hours will be provided over 8 weeks by licensed EMDR therapists from the German-speaking part of Switzerland. Each EMDR session follows a standardized 8-phase protocol.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 18-70 years * Men or women * STEMI (irrespective of troponin, but ST-elevation) or non-STEMI (troponin positive) at the time of the cardiac event, as verified by the cardiologist * Diagnosis of PTSD caused by the cardiac event Exclusion Criteria: * Psychotic disorder, bipolar disorder, substance abuse as measured with the Mini International Neuropsychiatric Interview (M.I.N.I) * Acute suicidal ideation as assessed with the M.I.N.I. * Non-selective beta blockers (e.g., propranolol) during the study period * Ongoing psychological/psychiatric treatment outside of the trial during the study period * Visionary problems, e.g. strabismus, which does not allow adequate eye movements * Insufficient knowledge of the German language * Expected inability or willingness to follow the study protocol * Regular medication with benzodiazepine

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Hospital Zurich Zurich Switzerland Recruiting

More University of Zurich trials in Switzerland

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04672551 on ClinicalTrials.gov ↗ ← All trials in Switzerland