Trauma-focused Therapies for Posttraumatic Stress in Psychosis: study protocol for the RE.PROCESS randomized controlled trial

Author:

Burger Simone Rosanne1ORCID,Linden Tineke van der2,Hardy Amy3,de Bont Paul A. J.4,Vleugel Berber van der5,Staring Anton B. P.6,de Roos Carlijn7,Zelst Catherine van8,Gottlieb Jennifer D.9,Mueser Kim10,Minnen Agnes van11,de Jongh Ad12,Marcelis Machteld13,Gaag Mark van der1,Berg David van den1

Affiliation:

1. Vrije Universiteit Amsterdam, Department of Clinical Psychology

2. Vrije Universiteit Amsterdam

3. Institute of Psychiatry at the Maudsley: King's College London Institute of Psychiatry Psychology and Neuroscience

4. GGZ Oost Brabant

5. GGZ Noord-Holland-Noord

6. Altrecht Foundation for Mental Health Care: Altrecht

7. Academic Centre for Child and Adolescent Psychiatry Levvel, Amsterdam University Medical Centre

8. Department of Psychosis Research and Innovation, Parnassia Psychiatric Institute, the Hague

9. Cambridge Health Alliance Department of Psychiatry

10. Boston University

11. Radboud Universiteit Behavioural Science Institute

12. ACTA: Academisch Centrum Tandheelkunde Amsterdam

13. Universiteit Maastricht Faculty of Health Medicine and Life Sciences

Abstract

Abstract Introduction: Many people with psychotic disorders experience symptoms of post-traumatic stress disorder (PTSD). In recent years, several trauma-focused therapies (TFTs), including cognitive restructuring (CR), prolonged exposure (PE), and eye movement desensitization and reprocessing (EMDR) have been studied and found to be safe and effective in reducing PTSD symptoms in individuals with psychosis. However, studies were conducted in different countries, with varying inclusion criteria, therapy duration, control groups, and trial outcomes. RE.PROCESS will be the first study to compare the impact of CR, PE and EMDR with a waiting list control condition within the same context.Methods and analysis: This is the protocol of a pragmatic, single-blind, multicentre, superiority randomized controlled trial, in which CR, PE, and EMDR are compared to a waiting list control condition for TFT (WL) in a naturalistic treatment setting. Inclusion criteria are: Age ≥ 16 years; meeting full DSM-5 diagnostic criteria for PTSD on the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5), with a total CAPS score ≥ 23; and a psychotic disorder in the schizophrenia spectrum confirmed by the Structured Clinical Interview for DSM-5 (SCID-5). Participants (N = 200) will be randomly allocated to 16 sessions of one of the TFTs or WL, in addition to receiving treatment as usual (TAU) for psychosis. The primary objective is to compare the effects of CR, PE, and EMDR to WL on researcher-rated severity of PTSD symptoms over time from baseline to 6-month follow-up. Secondary objectives are to examine these effects at the separate time-points (i.e. mid-treatment, post-treatment, and at 6-month follow-up) and to test the effects for clinician-rated presence of PTSD diagnosis, and self-rated severity of (complex) PTSD symptoms.Discussion: This is the first RCT to directly compare the effects of CR, PE and EMDR within the same context to TAU on PTSD symptoms in individuals with psychosis and PTSD. Secondary effects on clinical and functional outcomes will be investigated both directly after therapy and long-term.Trial registration: ISRCTN, ISRCTN56150327. Registered 18 June 2019, https://doi.org/10.1186/ISRCTN56150327

Publisher

Research Square Platform LLC

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