ID
Bron
Aandoening
Post-Traumatic Stress Disorder (PTSD)
Ondersteuning
(2) PsyQ Purmerend.
(3) Delft Technical University.
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
PTSD Checklist for DSM-5 (PCL-5)
Onderzoeksopzet
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.
Onderzoeksproduct en/of interventie
(1) Imagery Rescripting (active control treatment)
(2) Virtual Reality Imagery Rescripting (experimental treatment)
Publiek
University of Amsterdam
Weesperplein 4
A.A.P. Emmerik, van
Amsterdam 1018 XA
The Netherlands
+31-20-5256810
a.a.p.vanemmerik@uva.nl
Wetenschappelijk
University of Amsterdam
Weesperplein 4
A.A.P. Emmerik, van
Amsterdam 1018 XA
The Netherlands
+31-20-5256810
a.a.p.vanemmerik@uva.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- 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.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Other psychopathology that requires immediate other treatment or that would hinder study participation.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL6851 |
| NTR-old | NTR7029 |
| Ander register | : 2018-CP-8752 |