Posttraumatic Stress Disorder PTSD
Conditions
Interventions
This study entails two treatment conditions: the experimental 3MDR intervention
and conventional TF-PT. The 3MDR intervention is a new type of high intensive
exposure treatment, which combines eleme
Sponsors
ARQ Nationaal Psychotrauma Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: - Patients with work-related Posttraumatic Stress Disorder - 18 years or older - Meet the DSM-5 criteria for Posttraumatic Stress Disorder - Trauma-focused therapy naive - Master the Dutch language - Must be on a stable dose of medication at commencement of the trial for at least four weeks, and will be asked to keep the dosage stable during the trail.
Exclusion criteria
Exclusion criteria: - Inability to walk - Current severe alcohol or substance use disorder (SUD) - Acute suicidality - Acute psychosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary clinical outcome parameter is the difference in PTSD symptom severity measured prior to, during and after treatment. Furthermore, cost-effectiveness will be assessed through health-related quality of life and social costs. Our secondary outcomes include: avoidance behaviour, PTSD severity rated by a spouse, anxiety and depressive symptoms, impairment in daily functioning due to PTSD symptoms, neuropsychological functioning, and for the 3MDR condition physiological responses during sessions. | — |
Secondary
| Measure | Time frame |
|---|---|
| Our secondary outcomes include: avoidance behaviour, PTSD severity rated by a spouse, anxiety and depressive symptoms, impairment in daily functioning due to PTSD symptoms, neuropsychological functioning, and for the 3MDR condition physiological responses during sessions. | — |
Countries
Netherlands
Outcome results
None listed