A Study on the Efficacy of Virtual Reality Exposure Therapy (VRET) for Survivors of Childhood Sexual Abuse and War Related Trauma
Primary Purpose
Posttraumatic Stress Disorder (PTSD), Depression
Status
Unknown status
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
VRET
TAU
Sponsored by
About this trial
This is an interventional treatment trial for Posttraumatic Stress Disorder (PTSD) focused on measuring Posttraumatic Stress Disorder, Depression, Treatment, VRET
Eligibility Criteria
Inclusion Criteria:
- principal diagnosis meeting DSM-IV criteria for PTSD and/or major depression following CSA or war related trauma
- between the ages of 18 and 70-years-old
- having sufficient fluency in Dutch to complete treatment and research protocol
Exclusion Criteria:
- current bipolar disorder
- current psychotic disorders
- current suicidality
- high dissociation level (Dissociative Experiences Scale (DES) cut-off score ≥ 40)
Sites / Locations
- Reinier van Arkel Groep PTC ZNRecruiting
- PsyQRecruiting
- Erasmus University RotterdamRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
VRET
TAU
Arm Description
Virtual Reality Exposure Therapy (VRET) The experimental treatment VRET is offered with the Multi-Modal Memory Restructuring System (3MR system) and a therapy manual. Participants can use this system at home. Note: The 3MR system is offered via a computer screen, no head-mounted display (HMD) equipment is used in this study.
Treatment As Usual
Outcomes
Primary Outcome Measures
Posttraumatic Stress Disorder (PTSD) Checklist Diagnostic & Statistical Manual of Mental Disorders (DSM) 5 (PCL-5) to measure change from baseline self-reported symptoms of PTSD at the endpoint of the therapy (after completing 12 sessions) and follow-ups
The PCL-5 is a brief assessment that identifies the presence and symptom severity of PTSD. We use the PCL-5 to measure self-reported symptoms of PTSD.
Beck Depression Inventory-II (BDI-II) to measure change from baseline self-reported symptoms of depression at the endpoint of the therapy (after completing 12 sessions) and follow-ups
The BDI-II is a self-report questionnaire which measures the severity of depression in 21 statements, with four levels of increasing severity each. We use the BDI-II to measure self-reported symptoms of depression.
Secondary Outcome Measures
The Outcome Questionnaire-45-2 (OQ-45-2) to measure change from baseline self-reported symptoms and well-being at the endpoint of the therapy (after completing 12 sessions) and follow-ups
The OQ-45-2 is a questionnaire which measures well-being in three domains; symptom distress, interpersonal functioning and social role. We use the OQ-45-2 to measure improvement in well-being in participants as addition to the symptom checklists, and to make a useful translation of the research data into clinical practice.
Full Information
NCT ID
NCT02234076
First Posted
July 15, 2014
Last Updated
August 16, 2016
Sponsor
Erasmus Medical Center
Collaborators
Netherlands Organisation for Scientific Research, Erasmus University Rotterdam, Delft University of Technology, University of Amsterdam, PsyQ, Reinier van Arkel Groep, Psychotraumacentrum Zuid-Nederland
1. Study Identification
Unique Protocol Identification Number
NCT02234076
Brief Title
A Study on the Efficacy of Virtual Reality Exposure Therapy (VRET) for Survivors of Childhood Sexual Abuse and War Related Trauma
Official Title
A Study on the Efficacy of Virtual Reality Exposure Therapy (VRET) for Survivors of Childhood Sexual Abuse and War Related Trauma
Study Type
Interventional
2. Study Status
Record Verification Date
August 2016
Overall Recruitment Status
Unknown status
Study Start Date
October 2014 (undefined)
Primary Completion Date
October 2016 (Anticipated)
Study Completion Date
October 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Erasmus Medical Center
Collaborators
Netherlands Organisation for Scientific Research, Erasmus University Rotterdam, Delft University of Technology, University of Amsterdam, PsyQ, Reinier van Arkel Groep, Psychotraumacentrum Zuid-Nederland
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Background: Childhood Sexual Abuse (CSA) and combat related war-trauma are associated with posttraumatic stress disorder (PTSD) and depression. PTSD is one of the most prevalent Diagnostic and Statistical Manual of Mental Disorders (DSM) axis 1 disorders for which psychotherapy is widely practiced. Depression is one of the most common co morbid disorders when PTSD is diagnosed. Exposure to the traumatic memories or cues of the traumatic event often plays an important role in reducing symptoms of PTSD. Also symptoms of PTSD and depression have been related to a reduced specificity in autobiographical memory.
Objective: This study will examine the efficacy of a Virtual Reality Exposure Therapy (VRET) in a CSA and war related trauma sample by comparing it with treatment as usual (TAU). It will also attempt to develop protocols to implement this new technology into clinical practice and collect data to develop a treatment progress prediction model.
Study design: A randomized controlled intervention study.
Study population: 144 individuals with memories of CSA or war related trauma and symptoms of PTSD and/or depression.
Intervention: VRET or TAU.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Posttraumatic Stress Disorder (PTSD), Depression
Keywords
Posttraumatic Stress Disorder, Depression, Treatment, VRET
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
144 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
VRET
Arm Type
Experimental
Arm Description
Virtual Reality Exposure Therapy (VRET)
The experimental treatment VRET is offered with the Multi-Modal Memory Restructuring System (3MR system) and a therapy manual. Participants can use this system at home. Note: The 3MR system is offered via a computer screen, no head-mounted display (HMD) equipment is used in this study.
Arm Title
TAU
Arm Type
Active Comparator
Arm Description
Treatment As Usual
Intervention Type
Behavioral
Intervention Name(s)
VRET
Other Intervention Name(s)
Virtual Reality Exposure Therapy (VRET)
Intervention Type
Behavioral
Intervention Name(s)
TAU
Intervention Description
Treatment as usual offered by the participating mental health care organisations
Primary Outcome Measure Information:
Title
Posttraumatic Stress Disorder (PTSD) Checklist Diagnostic & Statistical Manual of Mental Disorders (DSM) 5 (PCL-5) to measure change from baseline self-reported symptoms of PTSD at the endpoint of the therapy (after completing 12 sessions) and follow-ups
Description
The PCL-5 is a brief assessment that identifies the presence and symptom severity of PTSD. We use the PCL-5 to measure self-reported symptoms of PTSD.
Time Frame
At pre (baseline), post (after 12 therapy sessions with a minimum of 6 weeks and a maximum of 12 weeks), and follow-up (3 and 12 months post treatment) measurements
Title
Beck Depression Inventory-II (BDI-II) to measure change from baseline self-reported symptoms of depression at the endpoint of the therapy (after completing 12 sessions) and follow-ups
Description
The BDI-II is a self-report questionnaire which measures the severity of depression in 21 statements, with four levels of increasing severity each. We use the BDI-II to measure self-reported symptoms of depression.
Time Frame
At pre (baseline), post (with a minimum of 6 weeks and a maximum of 12 weeks), and follow-up (3 and 12 months post treatment) measurements
Secondary Outcome Measure Information:
Title
The Outcome Questionnaire-45-2 (OQ-45-2) to measure change from baseline self-reported symptoms and well-being at the endpoint of the therapy (after completing 12 sessions) and follow-ups
Description
The OQ-45-2 is a questionnaire which measures well-being in three domains; symptom distress, interpersonal functioning and social role. We use the OQ-45-2 to measure improvement in well-being in participants as addition to the symptom checklists, and to make a useful translation of the research data into clinical practice.
Time Frame
At pre (baseline), post (with a minimum of 6 weeks and a maximum of 12 weeks) and follow up (3 and 12 months post treatment) measurements
Other Pre-specified Outcome Measures:
Title
The Positive and Negative Affect Scale (PANAS) to measure change in self-reported emotional progress between therapy sessions
Description
The PANAS is a self-report questionnaire to measure positive and negative affect. The PANAS measures specific feelings as 'interested', 'inspired' etc. We use the PANAS to measure change in these affects between therapy sessions.
Time Frame
Two times per week during 6 weeks
Title
The 9-item depression module of the Patient Health Questionnaire (PHQ) to measure self-reported emotional progress between therapy sessions
Description
The PHQ is a self-report questionnaire which scores the nine DSM-criteria for depression. We use the PHQ to measure change in the nine primary depression symptoms between therapy sessions.
Time Frame
Two times per week during 6 weeks
Title
The shortened version (6 items) of the PCL-5 to measure change in self-reported emotional progress between therapy sessions
Description
For general information PCL-5 see primary outcome section. We use 6 items of the PCL-5 to measure self-reported symptoms of PTSD between therapy sessions.
Time Frame
Two times per week during 6 weeks
Title
The self-report questionnaire Patient's acceptance of a Self-Management health system to asses participants' acceptance of the used technology
Description
The self-report questionnaire Patient's acceptance of a Self-Management health system is a questionnaire to evaluate participants' acceptance of the technology used during the current study. Outcomes are important because they might implicate alterations to strengthen usability of the technology.
Time Frame
Post treatment (after 6 weeks)
Title
The Mini International Neuropsychiatric Interview 5.0.0. (MINI 5.0.0.) Dutch version to screen for Diagnostic and Statistical Manual of Mental Disorder (DSM)-IV diagnoses
Description
The MINI 5.0.0. Dutch version is a semi-structured clinical interview to screen for DSM-IV diagnoses such as PTSD, major depression, bipolar disorder. We use the MINI 5.0.0. Dutch to check in- and exclusion criteria, and to determine change in diagnosis after therapy.
Time Frame
At pre (baseline), post (after 12 therapy sessions with a minimum of 6 weeks and a maximum of 12 weeks), and follow-up (3 and 12 months post treatment) measurements
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
principal diagnosis meeting DSM-IV criteria for PTSD and/or major depression following CSA or war related trauma
between the ages of 18 and 70-years-old
having sufficient fluency in Dutch to complete treatment and research protocol
Exclusion Criteria:
current bipolar disorder
current psychotic disorders
current suicidality
high dissociation level (Dissociative Experiences Scale (DES) cut-off score ≥ 40)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marieke van Meggelen, MSc
Phone
0031(0)10-4088689
Email
m.vanmeggelen@fsw.eur.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Ingmar Franken, full professor
Email
franken@fsw.eur.nl
Facility Information:
Facility Name
Reinier van Arkel Groep PTC ZN
City
Den Bosch
State/Province
Noord-Brabant
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marieke van Meggelen, MSc
Phone
0031(0)10-4088689
Facility Name
PsyQ
City
Rotterdam/The Hague
State/Province
Zuid-Holland
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marieke van Meggelen, MSc
Phone
0031(0)10-4088689
Facility Name
Erasmus University Rotterdam
City
Rotterdam
State/Province
Zuid-Holland
ZIP/Postal Code
3000 DR
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marieke van Meggelen, MSc
Phone
0031(0)10-4088689
12. IPD Sharing Statement
Links:
URL
http://ii.tudelft.nl/vesp/
Description
Project website
Learn more about this trial
A Study on the Efficacy of Virtual Reality Exposure Therapy (VRET) for Survivors of Childhood Sexual Abuse and War Related Trauma
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