Status:

NOT_YET_RECRUITING

Neurofeedback and Well-Being Among People With Co-Occurring Obsessive Compulsive Disorder and Post-traumatic Stress Symptoms

Lead Sponsor:

Wayne State University

Conditions:

Well-Being, Psychological

Mood Disturbance

Eligibility:

All Genders

18-90 years

Phase:

NA

Brief Summary

The proposed study will collect novel data evaluating the feasibility of a neurofeedback training program delivered to prospective clients with a history of clinically concerning trauma-related mental...

Eligibility Criteria

Inclusion

  • being a client placed on the clinic waitlist to receive exposure-response prevention for OCD symptoms at the Anxiety and OCD Treatment Center of Ann Arbor, in Ann Arbor, MI.
  • having self-reported symptoms of OCD;
  • having post-traumatic stress symptoms as indicated by a score of 3 or higher on the Primary Care PTSD Screen for DSM-5 (PC-PTSD-5) screening measure;
  • being age 18+.
  • being a citizen of the United States of America -

Exclusion

  • a lifetime history of significant untreated mental illness (not currently treated schizophrenia, schizoaffective disorder, bipolar disorder, or substance use disorder) or neurological or pervasive developmental disorder;
  • a documented history of epilepsy;
  • lifetime history of any head injury with loss of consciousness;
  • current exposure domestic or intimate partner violence or otherwise state that their current living conditions are unsafe;
  • current experiences of psychosis or suicidality within the last six months;
  • currently taking, or in the past month has taken benzodiazepines, narcotic drugs, or cannabis;
  • currently pregnant
  • engagement in self-harming behaviors in the last 3 months that required medical attention;
  • lack of competence to understand or consent to the study procedures;
  • lack of fluency in written and spoken English. -

Key Trial Info

Start Date :

November 1 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

January 1 2029

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT07217925

Start Date

November 1 2025

End Date

January 1 2029

Last Update

November 12 2025

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