Decrease Trauma-related Shame With Virtual Reality: The Effectiveness of SHINE-VR

NCT ID: NCT06384508

Last Updated: 2025-12-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

6 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-03

Study Completion Date

2025-05-19

Brief Summary

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Suffering from PTSD in childhood can have detrimental formative consequences. Researchers have been eager to develop effective interventions and to enhance treatment motivation since the introduction of the diagnosis of PTSD in the DSM. With evolving understanding of the disorder, its definition and criteria have changed over the course of time. The most recent change involves the addition of the criterium D of negative affects or emotions in relation to PTSD, the feeling of shame amongst others. Individuals experiencing interpersonal trauma, such as sexual abuse, are at high-risk developing trauma-related shame, which in turn can impact the course and effectiveness of PTSD treatment. Shame-inducing situations are typically being avoided, and the feelings are not disclosed to peers and other people. Hence, acknowledging and sharing feelings of shame as well as practicing self-compassion have been proposed to reduce the impact of that negative self-conscious emotion. These aspects get partially tackled in evidence-based trauma therapies, however, there appears to be a need for a more specific trauma-related shame intervention in addition to existing treatments. Recent research has focused on developing such interventions for adults and has reported positive effects.

To our knowledge, there is no intervention specifically tackling trauma-related shame in adolescents. Virtual Reality (VR) is a promising tool for such an intervention. Findings suggest that including VR in a treatment results in high treatment satisfaction and that it is highly motivating for its users, which is a crucial component for treatment success.

The goal of this study is to test the effectiveness of a short-term VR shame intervention (SHINE-VR) for adolescents suffering from PTSD after having experienced sexual abuse. The primary objectives of this study to assess the effect of SHINE-VR on trauma-related shame, self-compassion, and PTSD symptom reduction, to investigate whether treatment motivation, an increase in self-compassion, and a decrease in trauma-related shame are associated with PTSD symptom reduction.

Detailed Description

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Conditions

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Shame

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Single Case Experimental Design (ABC) with two different baseline lengths
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
The participants are unaware of different baseline lengths

Study Groups

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SHINE-VR Baseline 1 week

Participants will receive SHINE-VR additionally to regular trauma treatment. The baseline phase starts after trauma processing, e.g. after module 6 of TF-CBT or processing of the traumatic event with EMDR.

This group has a one week baseline, 3 weeks intervention, and 2 week follow-up phase.

Group Type ACTIVE_COMPARATOR

SHINE-VR

Intervention Type BEHAVIORAL

The SHINE-VR takes place after trauma processing, e.g. after module 6 of TF-CBT or processing of the traumatic event with EMDR, and is followed by the rest of the regular treatment. SHINE-VR consists of the following 3 VR sessions à 45min:

* Introduction: getting acquainted with VR, playing a VR game developed for the feasibility study (Krupljanin et al., in preparation), receiving psychoeducation about seeking help.
* Shame: virtual group therapy setting, psychoeducation about shame, virtual peers sharing thoughts of shame and their learnings/positive affirmations.
* Self-compassion: practicing self-compassion using an immersive perspective-changing task in VR.

SHINE-VR Baseline 2 weeks

Participants will receive SHINE-VR additionally to regular trauma treatment. The baseline phase starts after trauma processing, e.g. after module 6 of TF-CBT or processing of the traumatic event with EMDR.

This group has a two week baseline, 3 weeks intervention, and a 1 week follow-up phase.

Group Type ACTIVE_COMPARATOR

SHINE-VR

Intervention Type BEHAVIORAL

The SHINE-VR takes place after trauma processing, e.g. after module 6 of TF-CBT or processing of the traumatic event with EMDR, and is followed by the rest of the regular treatment. SHINE-VR consists of the following 3 VR sessions à 45min:

* Introduction: getting acquainted with VR, playing a VR game developed for the feasibility study (Krupljanin et al., in preparation), receiving psychoeducation about seeking help.
* Shame: virtual group therapy setting, psychoeducation about shame, virtual peers sharing thoughts of shame and their learnings/positive affirmations.
* Self-compassion: practicing self-compassion using an immersive perspective-changing task in VR.

Interventions

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SHINE-VR

The SHINE-VR takes place after trauma processing, e.g. after module 6 of TF-CBT or processing of the traumatic event with EMDR, and is followed by the rest of the regular treatment. SHINE-VR consists of the following 3 VR sessions à 45min:

* Introduction: getting acquainted with VR, playing a VR game developed for the feasibility study (Krupljanin et al., in preparation), receiving psychoeducation about seeking help.
* Shame: virtual group therapy setting, psychoeducation about shame, virtual peers sharing thoughts of shame and their learnings/positive affirmations.
* Self-compassion: practicing self-compassion using an immersive perspective-changing task in VR.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Between 12 and 17 years old at inclusion
* Interpersonal trauma (sexual abuse); in case of multiple traumas the main trauma should be sexual abuse
* Indication for PTSD treatment
* Getting trauma treatment as usual
* Adequate command of the Dutch language

Exclusion Criteria

* Known mental disability
* Epilepsy
Minimum Eligible Age

12 Years

Maximum Eligible Age

17 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Amsterdam

OTHER

Sponsor Role collaborator

Universiteit Leiden

OTHER

Sponsor Role lead

Responsible Party

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Carlijn Bergwerff

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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GGZ Delfland

The Hague, Haaglanden, Netherlands

Site Status

iMindU Practice for Child, Adolescent and Adult Psychiatry

Leiden, South Holland, Netherlands

Site Status

LEVVEL

Amsterdam, , Netherlands

Site Status

Kenter Jeugdhulp

Haarlem, , Netherlands

Site Status

LUMC Curium

Oegstgeest, , Netherlands

Site Status

Countries

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Netherlands

References

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Aakvaag HF, Thoresen S, Wentzel-Larsen T, Dyb G, Roysamb E, Olff M. Broken and guilty since it happened: A population study of trauma-related shame and guilt after violence and sexual abuse. J Affect Disord. 2016 Nov 1;204:16-23. doi: 10.1016/j.jad.2016.06.004. Epub 2016 Jun 11.

Reference Type RESULT
PMID: 27318595 (View on PubMed)

Neff KD, Bluth K, Toth-Kiraly I, Davidson O, Knox MC, Williamson Z, Costigan A. Development and Validation of the Self-Compassion Scale for Youth. J Pers Assess. 2021 Jan-Feb;103(1):92-105. doi: 10.1080/00223891.2020.1729774. Epub 2020 Mar 3.

Reference Type RESULT
PMID: 32125190 (View on PubMed)

Sachser C, Berliner L, Risch E, Rosner R, Birkeland MS, Eilers R, Hafstad GS, Pfeiffer E, Plener PL, Jensen TK. The child and Adolescent Trauma Screen 2 (CATS-2) - validation of an instrument to measure DSM-5 and ICD-11 PTSD and complex PTSD in children and adolescents. Eur J Psychotraumatol. 2022 Aug 1;13(2):2105580. doi: 10.1080/20008066.2022.2105580. eCollection 2022.

Reference Type RESULT
PMID: 35928521 (View on PubMed)

Drieschner KH, Boomsma A. Validation of the Treatment Motivation Scales for Forensic outpatient treatment (TMS-F). Assessment. 2008 Jun;15(2):242-55. doi: 10.1177/1073191107311651. Epub 2008 Feb 1.

Reference Type RESULT
PMID: 18245208 (View on PubMed)

Other Identifiers

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NL83340.058.23

Identifier Type: -

Identifier Source: org_study_id

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