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

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

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02757339
Enrollment
200
Registered
2016-05-02
Start date
2015-06-01
Completion date
2027-06-01
Last updated
2026-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dissociative Identity Disorder, Posttraumatic Stress Disorders

Keywords

neurobiology, PTSD, DID

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

Mclean Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 89 Years
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline correlates of traumatic dissociation in Functional Magnetic Resonance Imaging at 36 to 56 weeksBaseline and 36 to 56 weeks after baselineStudy 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.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORMilissa L Kaufman, M.D./Ph.D

Mclean Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 26, 2026