Investigating a digital device to increase the efficiency of trauma-focused psychotherapy in PTSD patients: a pilot randomized controlled trial of the EMD app.
- Conditions
- posttraumatic stress disorderPTSD10002861
- Registration Number
- NL-OMON47137
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Trial is onging in other countries
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 57
- 18 * 65 years of age or older
- Referred to a mental health care organisation for PTSD following one or more traumatic experiences
- Meet the DSM-5 diagnostic criteria for PTSD as confirmed by the CAPS-5
- Are in possession of a device such as a laptop, tablet, mobile phone or computer
- Have sufficient command of the Dutch language, both verbally and in writing
- Provide signed informed consent
- Having current high risk for suicide according to the M.I.N.I. Interview for psychiatric disorders, section C
- Having serious psychiatric co-morbidity i.e. bipolar affective disorder, psychotic disorder, substance dependence that would interfere with EMDR treatment as assessed by the therapist in the intake.
- Being unable to comprehend the spoken and written Dutch language.
- Not having access to a computer, laptop, tablet or smartphone with an internet connection.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary outcome parameter is the difference in PTSD symptom severity<br /><br>response pattern during the five sessions between the EMDR + EMD app group as<br /><br>compared to the EMDR alone group. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary outcomes include depressive symptoms, general anxiety symptoms,<br /><br>acceptability, usability and client satisfaction.</p><br>