Post-Traumatic Stress Disorder (PTSD) Clinical Trials

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

Status: Recruiting
Location: See location...
Intervention Type: Behavioral, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Canada
100 Stokes St
RECRUITING
Toronto
Time Frame
Start Date: 2026-01-20
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 24
Treatments
Experimental: A-EMDR
Placebo_comparator: Regular care
Related Therapeutic Areas
Sponsors
Leads: Centre for Addiction and Mental Health

This content was sourced from clinicaltrials.gov