Digital cue-based technique with eye movements for intrusive memories after trauma
Official title: A Novel Digital Cognitive Intervention Targeting Intrusive Memories Among Trauma-Exposed Individuals: A Randomised Clinical Trial
Run by Shaanxi Normal University · NCT07523360 · Data updated 2026-11-12
This online study tests a light, non- distressing intervention using visual cues and eye movements to see if it reduces frequent intrusive memories in people with PTSD.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 50 Years |
| Sex | All |
| Enrollment | 123 (estimated) |
| Sponsor | Shaanxi Normal University Academic / other |
| Locations | 1 site (Xi'an, Shaanxi) |
| Status | Recruiting |
| Started | June 10, 2026 |
| Main results expected | April 10, 2028 |
| Study ends | July 10, 2028 |
| Registry record updated | September 2, 2026 |
| Trial ID | NCT07523360 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with PTSD who experience at least five intrusive memories per week and have internet access and a personal computer.
✕Probably not a fit
Individuals without frequent intrusive memories or who do not meet other criteria may not experience a benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The study uses a randomized, three-arm design to compare trauma-related images, participant-provided images, and neutral images, each paired with bilateral eye movements. It targets adults with PTSD who experience at least five intrusive memories per week and have internet access, aiming to enroll about 40 participants per arm. The primary outcome is the weekly frequency of intrusive memories, with secondary outcomes including PTSD severity measured by CAPS-5. Data will be collected online for efficiency and safety, with an emphasis on minimizing distress during the intervention. The study is conducted at Shaanxi Normal University in Xi'an, led by Zhu Zijian.
Why it matters
Potential benefit: If successful, the intervention could offer a less aversive option to reduce intrusive memories and PTSD symptoms.
How similar studies have gone: Previous work in similar eye-movement and cue-based approaches has shown promise in reducing intrusive memories, but this specific online, three-arm design is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Meet the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) Criterion A for post-traumatic stress disorder (PTSD), which requires exposure to an event involving serious injury or a threat to one's own or another person's physical well-being, either through direct experience or witnessing. 2. Exhibit symptoms from at least three of the five core PTSD symptom domains outlined in DSM-5: intrusive memories (Criterion B), persistent avoidance of trauma-related stimuli (Criterion C), negative alterations in cognitions and mood (Criterion D), alterations in arousal and reactivity (Criterion E), and symptoms lasting for at least one month (Criterion F). 3. Have a total score of 33 or higher on the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5). 4. Have internet access and access to a personal computer. 5. Have not taken part in a previous study of this intervention conducted by this research team. Exclusion Criteria: 1. Fewer than 5 intrusive memories during the baseline week (Week 0). 2. An intelligence quotient (IQ) score lower than 80. 3. A current diagnosis of schizophrenia, obsessive-compulsive disorder (OCD), a severe personality disorder judged to interfere with treatment adherence, or acute suicidal behavior. 4. Severe substance dependence.
Where it's running
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School of Psychology, Shaanxi Normal University
Xi'an, Shaanxi, China Recruiting
Study contacts
- Study coordinator: Zijian Zhu
- Email: zhuzijian0203@snnu.edu.cn
- Phone: +86 13572494696
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.