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Enrolling by Invitation

NCT Number: NCT02757339

Evaluating the Neurobiological Basis of Traumatic Dissociation in Women With Histories of Abuse and Neglect

This study aims to evaluate the neurobiological basis of traumatic dissociation in a cross-diagnostic sample of women who have histories of childhood abuse and neglect.

Enrolling by Invitation

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Key information

Age range

18 year–89 year

Sex eligibility

Female

Study type

Observational

Primary location

McLean Hospital

Belmont, Massachusetts, 02478, United States

About this study

Dissociative symptoms commonly are associated with exposure to traumatic stress. Preliminary evidence from functional magnetic resonance imaging-based analysis (fMRI) of neural activation during dissociative symptom provocation in patients with PTSD or DID has implicated certain key structures involved in the generation of dissociative symptoms. Given the presumed region-to-region neural interplay implicit within this model, the investigators believe the use of intrinsic functional connectivity MRI (fcMRI) represents a valuable next line of investigation into the neurobiology of traumatic dissociation. The investigators also believe that a genetic approach holds promise as another converging line of inquiry into our understanding of traumatic dissociation.

To evaluate the neurobiological basis of traumatic dissociation, this study will recruit patients with PTSD or DID, and recruit matched controls to identify neurobiological correlates of traumatic dissociation.The study will compare the phenomenology of traumatic dissociation in patients with different PTSD subtypes and DID using standardized measures to look at the neurological and genetic correlates.

This study will also include a follow up visit that includes neuroimaging and genetic assessments.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female
  • Clinical diagnosis of PTSD or DID and history of childhood abuse, or healthy controls
  • Age between 18 and 89
  • Legal and mental competency of the patient

Exclusion criteria

  • Male
  • Under 18 or over 89
  • Legal or mental incompetence
  • Delirium secondary to medical illness
  • PTSD or DID due to general medical or neurological illness
  • History of neurological conditions that may cause significant psychiatric symptomatology (e.g., dementia)
  • Any contraindication to MR scans, including claustrophobia, pregnancy, metal implants, etc.
  • Current alcohol or substance dependence or abuse (within the last month)
  • A history of schizophrenia or other psychotic disorder
  • History of head injury or loss of consciousness for longer than 5 min (including concussion)

Treatment and study plan

Primary outcomes

  1. Change from Baseline correlates of traumatic dissociation in Functional Magnetic Resonance Imaging at 36 to 56 weeks

    Time frame: Baseline and 36 to 56 weeks after baseline

    Study participation will involve a baseline 60 minute cognitive assessment and a 60 minute Magnetic Resonance Imaging (MRI) at the 3 Tesla magnet in the McLean Hospital Imaging Center focusing on attention, emotion regulation, and symptoms of depersonalization. The first time point is baseline.The second time point will be 36-56 weeks after the baseline 60 minute Magnetic Resonance Imaging (MRI) scan at the 3 Tesla magnet in the McLean Hospital Imaging Center.

Sponsors and collaborators

Lead sponsor

Mclean Hospital

Other

Registry information

Official study title

Evaluating the Neurobiological Basis of Traumatic Dissociation in a Cross-Diagnostic Sample of Women With Histories of Childhood Abuse and Neglect

Important dates

Study start
2015
Primary completion
2027
Study completion
2027
First posted
May 2, 2016
Registry last updated
Jun 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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