No registrations found.
ID
Source
Health condition
Post-Traumatic Stress Disorder (PTSD)
Sponsors and support
(2) PsyQ Purmerend.
(3) Delft Technical University.
Intervention
Outcome measures
Primary outcome
PTSD Checklist for DSM-5 (PCL-5)
Secondary outcome
Hospital Anxiety and Depression Scale (HADS)
Post-Traumatic Cognitions Inventory (PTCI)
Non-fear emotion (e.g., guilt, anger, shame) items (added to PCL-5)
Study design
Primary outcome (PCL-5) is administered weekly troughout the study.
Secondary outcomes are administered at every study phase change.
Presence of PTSD is assessed at the start (when evaluating the in-/exclusion criteria) and end of the study.
Intervention
(1) Imagery Rescripting (active control treatment)
(2) Virtual Reality Imagery Rescripting (experimental treatment)
University of Amsterdam
Weesperplein 4
A.A.P. Emmerik, van
Amsterdam 1018 XA
The Netherlands
+31-20-5256810
a.a.p.vanemmerik@uva.nl
University of Amsterdam
Weesperplein 4
A.A.P. Emmerik, van
Amsterdam 1018 XA
The Netherlands
+31-20-5256810
a.a.p.vanemmerik@uva.nl
Inclusion criteria
- Primary diagnosis of PTSD, as established with a structured diagnostic interview (MINI, SCID, or CAPS).
- Index trauma is childhood (<16) sexual abuse.
- Conventional ImRs should be an appropriate treatment if patients were treated outside of the study.
- 16 years or older.
- Sufficient fluency in Dutch to complete research procedures (informed consent and study measures).
- Willingness to provide written informed consent.
Exclusion criteria
- Other psychopathology that requires immediate other treatment or that would hinder study participation.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL6851 |
| NTR-old | NTR7029 |
| Other | : 2018-CP-8752 |