Virtual reality could open doors to trauma therapy
NCT ID NCT06684977
First seen Aug 17, 2026 · Last updated Aug 18, 2026 · Updated 1 time
Summary
This study tests whether low-cost virtual reality (VR) tools, like 360° video and a new VR Photoscan process, can help people with post-traumatic stress disorder (PTSD) engage more easily with trauma-focused therapy. Participants will receive standard therapy (TF-CBT) either alone or with the addition of a personalized VR environment designed to help them revisit and process traumatic memories. The goal is to see if this approach is feasible and acceptable to patients and therapists, potentially making VR a practical tool in routine mental health care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Low-cost virtual reality environments using 360° video or VR Photoscan, used alongside standard trauma-focused cognitive behavioural therapy (TF-CBT)
- What this could lead to
- If this works, it could offer a low-cost, practical way to help people with PTSD engage more easily with trauma-focused therapy, potentially improving treatment outcomes.
- What could go wrong
- This is a very small feasibility study with only 15 participants, so results may not apply broadly. The technology may not be acceptable or effective for everyone, and there are risks like motion sickness or discomfort.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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15 people
The number who actually took part.
- Started
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Jun 2024
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults who self-report the experience of type 1 trauma (NI related) * PTSD symptoms as identified via PCL-5 \> 31 * Ability to give informed consent * Suitable and willingness to engage in TF-CBT * Scene of the traumatic event is accessible for 360° video or VR Photoscan Exclusion Criteria: * History of severe motion sickness * History of seizures, seizure disorder, or epilepsy * History of bipolar disorder, psychosis, or schizophrenia * Younger than 18 years old * Experiences their trauma at a site that is not accessible (i.e., would not be possible to capture images) * Previously engaged in TF-CBT within the PTS in the past 12 months * Actively suicidal or undertaken suicidal action in the past 3 months
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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South Eastern Health and Social Care Trust (Regional Trauma Network)
Belfast, Dundonald, BT16 1RH, United Kingdom
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Other studies related to the condition(s) this trial covers.
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