Clinical trial Recruiting at 1 site Interventional Ages 18 and up

An EMDR app for PTSD in people with substance dependence.

Official title: Efficacy and Feasibility of Autonomous Eye Movement Desensitization and Reprocessing (A-EMDR) for Patients With Posttraumatic Stress Disorder (PTSD) and Substance Use Disorders

Run by Centre for Addiction and Mental Health · NCT07146633 · Data updated 2026-11-12

This project will test whether an app-based autonomous EMDR program helps adults with PTSD who also have a substance use disorder.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment24 (estimated)
SponsorCentre for Addiction and Mental Health
Academic / other
Locations1 site (Toronto, Ontario)
StatusRecruiting
StartedJanuary 20, 2026
Main results expectedJanuary 30, 2027
Study endsJanuary 30, 2027
Registry record updatedMay 22, 2026
Trial IDNCT07146633 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) who are fluent in English, have PTSD with a PCL-5 score >32, a past-year substance use disorder (other than caffeine), are medically stable, and have no current suicidal risk or acute psychosis/mania are the best fits for this study.

Probably not a fit

People with severe or unstable mental illness, current suicidal risk, non–English speakers, or those unable or unwilling to attend in-person visits or pause other new behavioral therapies are unlikely to benefit from this pilot.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This open-label pilot randomized, wait-list controlled study tests autonomous eye movement desensitization and reprocessing (A-EMDR) delivered via an app in adults with PTSD and a co-occurring substance use disorder. Participants are randomized to four weeks of A-EMDR plus treatment-as-usual (TAU) or a wait-list TAU arm, with primary outcomes measured at week 4 and a follow-up at week 8 for the A-EMDR group. Enrollment requires adults with PCL-5 scores >32 and a past-year SUD, and excludes those with unstable severe mental illness or current suicidality. Feasibility, safety, and symptom change data will guide whether a larger definitive trial is warranted.

Why it matters

Potential benefit: If effective, the app could provide a brief, low-cost PTSD treatment option that is easier to scale for people with co-occurring substance use disorders.

How similar studies have gone: Face-to-face EMDR has established evidence for PTSD, but autonomous or app-delivered EMDR is relatively novel and has limited prior testing, particularly in populations with co-occurring substance use disorders.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Aged 18-years old or older
* Fluent in English
* Diagnosed with PTSD by the PTSD Checklist for DSM-5 (PCL-5 past month version score \>32)
* Diagnosed with past-year substance use disorder other than caffeine by structured clinical interview for DSM-5 (SCID-5)
* Agrees not to participate in other treatments during the study duration (e.g., mindfulness, yoga, biofeedback, self-hypnosis or tai chi) except individuals who have been already on continuous therapies for at least three months

Exclusion Criteria:

* Diagnosis of a severe or unstable mental illness that precludes safe participation in the study by a healthcare practitioner such as acute psychosis or mania diagnosed by a healthcare practitioner
* Current suicidality risk as indicated during the conduct of the Columbia Suicide Severity Rating Scale (C-SSRS) (21) with concurrence after a study physician's evaluation if the response to C-SSRS questions 1 or 2 is "yes"

Where it's running

  • 100 Stokes St
    Toronto, Ontario, Canada
    Recruiting

Similar studies

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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.