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Study identifier: NCT06806267 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of the Effectiveness of VRET Combined With tDCS in the Treatment of PTSD in Ukrainian Veterans and Civilians

Condition: PTSD - Post Traumatic Stress Disorder  ·  Sponsor: Malek Bajbouj

PhaseNA
Planned participants514
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

A new method is being tested to assist individuals in Ukraine with Post-Traumatic Stress Disorder (PTSD), including veterans and civilians affected by war. The study is a collaboration among Ukrainian healthcare institutions and the Charité Berlin. What is PTSD? PTSD can occur after a distressing or traumatic experience, such as exposure to war. It can result in persistent negative memories, nightmares, heightened nervousness, or avoidance of reminders associated with the event. Purpose of the Study Two innovative treatments for PTSD are being tested: 1. Virtual Reality Therapy: This approach uses specialized goggles to create a safe and realistic virtual environment where individuals can confront memories and process emotions with guidance from a therapist. 2. Brain Stimulation Therapy (tDCS): This method applies a gentle electrical current to the scalp to support improved emotional regulation by the brain. The study aims to determine whether combining these two treatments is more effective than using virtual reality therapy alone. Participant Involvement Participants will: * Attend 10 therapy sessions over several weeks. * Use virtual reality goggles to engage with safe scenarios related to their memories, guided by a therapist. * Potentially receive brain stimulation therapy during some virtual reality sessions. * Learn relaxation techniques to help manage stress and enhance emotional control. Potential Benefits for Participants * These treatments may reduce sym…

This description comes directly from the study's public registry record.

Talk to the study team

Yuliya Kovalchuk, M.Sc.  ·  +4915777013849  ·  yuliya.kovalchuk@charite.de

Always discuss trial participation with your own doctor first.

Locations (1)

Charité - Universitätsmedizin BerlinBerlin, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT06806267