Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07146633

Efficacy of an EMDR App for PTSD and SUD

Led by Centre for Addiction and Mental Health · Updated on 2026-02-12

24

Participants Needed

1

Research Sites

101 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The current proposal is aimed to confirm the efficacy of this novel therapeutic method (autonomous eye movement desensitization and reprocessing; A-EMDR) in a patient group (PTSD and SUD), and to assess the feasibility of the application within this group. While there is no basis to assume lower efficacy of the treatment with this population, confirming that hypothesis is an important and helpful step before a full-performance research study can be initiated. Furthermore, this study proposal will provide additional information regarding the feasibility for this population, which will allow for a more tailored approach in future study.

CONDITIONS

Official Title

Efficacy of an EMDR App for PTSD and SUD

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Fluent in English
  • Diagnosed with PTSD by PTSD Checklist for DSM-5 (PCL-5) past month version score greater than 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 study except those on continuous therapies for at least three months
Not Eligible

You will not qualify if you...

  • Diagnosis of severe or unstable mental illness preventing safe participation, such as acute psychosis or mania
  • Current suicidality risk as indicated by Columbia Suicide Severity Rating Scale (C-SSRS) and confirmed by study physician if responses to questions 1 or 2 are yes

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

100 Stokes St

Toronto, Ontario, Canada

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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