Clinical trial Recruiting at 1 site Interventional Ages 18 to 50

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 typeInterventional
Ages18 Years to 50 Years
SexAll
Enrollment123 (estimated)
SponsorShaanxi Normal University
Academic / other
Locations1 site (Xi'an, Shaanxi)
StatusRecruiting
StartedJune 10, 2026
Main results expectedApril 10, 2028
Study endsJuly 10, 2028
Registry record updatedSeptember 2, 2026
Trial IDNCT07523360 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

  • School of Psychology, Shaanxi Normal University
    Xi'an, Shaanxi, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.