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NCT05244564 · ClinicalTrials.gov registry record · NA

Computer Monitor vs Augmented Reality 3MDR for PTSD PTSD: A Randomized Controlled Trial

A NA study of Stress Disorders, Post-Traumatic, sponsored by Uniformed Services University of the Health Sciences.

Recruiting
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT05244564: Recruiting NA study of Stress Disorders, Post-Traumatic, sponsored by Uniformed Services University of the Health Sciences.

NCT05244564 is a NA study of Stress Disorders, Post-Traumatic that is actively recruiting participants, run by Uniformed Services University of the Health Sciences. The registered enrollment target is 60 participants, below the 155-participant average among 66 other Stress Disorders, Post-Traumatic trials with a reported enrollment target (61% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05244564, a NA study of Stress Disorders, Post-Traumatic, is actively recruiting participants, sponsored by Uniformed Services University of the Health Sciences.

RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

This is a prospective randomized controlled trial comparing two ways of delivering Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR) therapy for posttraumatic stress disorder (PTSD). The study seeks 60 volunteers who have PTSD and are eligible for care in the Department of Defense healthcare system. There will be 10-14 therapy sessions that are 60-90 minutes long, about once a week, and symptoms will be assessed before and after the therapy as well as 3 and 6 months after completing therapy. 3MDR asks you to choose pictures and music that are integrated into a virtual reality environment. You will be walking on a treadmill throughout each therapy session, while the therapist stands next to the treadmill and asks you questions about the pictures you chose.

Primary Outcome

The primary outcome measure will be the Clinician Administered PTSD scale for DSM5 (CAPS-5), the gold standard measure for PTSD diagnosis, to assess PTSD symptom severity.

Conditions Studied

Stress Disorders, Post-Traumatic

Interventions

  • OTHER Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR)

Study Locations (1)

Maryland

  • Uniformed Services University - Bethesda

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2023-04-30
Est. Completion 2027-10-30
Phase NA
Uniformed Services University of the Health Sciences

27 total trials

What NCT05244564 shows while recruiting

NCT05244564 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 155-participant average among 66 other Stress Disorders, Post-Traumatic trials with a reported enrollment target (61% lower).

The record links to 1 condition, with Stress Disorders, Post-Traumatic appearing as the primary indexed condition, and to 1 intervention - of which Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR) is the first listed.

NCT05244564 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT05244564 about?

NCT05244564 is a clinical study titled "Computer Monitor vs Augmented Reality 3MDR for PTSD PTSD: A Randomized Controlled Trial". This is a prospective randomized controlled trial comparing two ways of delivering Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR) therapy for posttraumatic stress disorder (PTSD). The study seeks 60 volunteers who have PTSD and are eligible for care in the Departmen...

What is the current status of trial NCT05244564?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2023-04-30. Estimated completion is 2027-10-30.

What conditions does trial NCT05244564 study?

This clinical trial studies the following conditions: Stress Disorders, Post-Traumatic.

What interventions are being tested in trial NCT05244564?

The interventions under investigation include: Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR) (OTHER).

Who is sponsoring clinical trial NCT05244564?

This trial is sponsored by Uniformed Services University of the Health Sciences, which has 27 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05244564 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Learn More About Clinical Trials

Similar trials for Stress Disorders, Post-Traumatic

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05244564's enrollment target sits among peer trials

60 43rd of 66 higher than 22 of 66 other Stress Disorders, Post-Traumatic trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Stress Disorders, Post-Traumatic trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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More recruiting context for NCT05244564

Source: ClinicalTrials.gov NCT05244564, the US trial registry maintained by the National Library of Medicine. NCT05244564 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.