NCT05788302

Brief Summary

The primary objective of this research is to collect pilot data that demonstrates that proposed neural, psychophysiological and subjective markers measured before, during, and after treatment change over the course of Prolonged Exposure therapy (PE) for posttraumatic stress disorder (PTSD). The aims of the study are to: (1) examine theoretically informed mechanisms as pretreatment predictors of PE treatment efficacy, (2) characterize how neural, psychophysiological, and subjective markers measured before, during, and after treatment change over the course of PE, and (3) examine proposed mechanisms of change as measures of PE treatment efficacy. This is a longitudinal study of predictors of exposure therapy efficacy that will be conducted within the context of a standard 10 session PE treatment trial, with independent multimodal assessment batteries administered at pre-treatment, mid-treatment, post-treatment, and at 1-month follow-up. This data will be used to support a future NIMH and/or VA grant submission.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
19mo left

Started Apr 2023

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress66%
Apr 2023Dec 2027

First Submitted

Initial submission to the registry

March 8, 2023

Completed
20 days until next milestone

First Posted

Study publicly available on registry

March 28, 2023

Completed
4 days until next milestone

Study Start

First participant enrolled

April 1, 2023

Completed
3.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2027

Expected
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2027

Last Updated

November 13, 2025

Status Verified

September 1, 2025

Enrollment Period

3.9 years

First QC Date

March 8, 2023

Last Update Submit

November 12, 2025

Conditions

Keywords

Post Traumatic Stress DisorderExposure Therapy

Outcome Measures

Primary Outcomes (1)

  • Change from baseline in Clinician Administered PTSD Scale for DSM-5 (CAPS-5)

    The primary clinical outcome, CAPS-5, is the gold standard clinical interview for assessing PTSD severity. In CAPS-5, each of the 20 symptoms of PTSD is rated on a 5-point severity scale ranging from 0 (absent) to 4 (extreme). Total scores range from 0 to 80.

    Given during screening session, pre-treatment, mid-treatment (post session 5 in week 5 of treatment), post-treatment (post session 10 in week 10 of treatment), and at 1-month follow up.

Secondary Outcomes (8)

  • PTSD Checklist for DSM-5 (PCL-5)

    Given during screening session, pre-treatment, mid-treatment (post session 5 in week 5 of treatment), post-treatment (post session 10 in week 10 of treatment), and at 1-month follow up.

  • Quick Inventory of Depressive Symptomatology - Self report (QIDS-SR)

    Given during screening session, pre-treatment, mid-treatment (post session 5 in week 5 of treatment), post-treatment (post session 10 in week 10 of treatment), and at 1-month follow up.]

  • Prefrontal cortical activity during script-driven imagery (SDI)

    Given during screening session, pre-treatment, mid-treatment (post session 5 in week 5 of treatment), post-treatment (post session 10 in week 10 of treatment), and at 1-month follow up.

  • Change in electrocardiography (ECG) and heart rate variability (HRV) during script driven imagery (SDI)

    Given during screening session, pre-treatment, mid-treatment (post session 5 in week 5 of treatment), post-treatment (post session 10 in week 10 of treatment), and at 1-month follow up.]

  • Change in skin conductance (SC) during script-driven imagery (SDI)

    Given during screening session, pre-treatment, mid-treatment (post session 5 in week 5 of treatment), post-treatment (post session 10 in week 10 of treatment), and at 1-month follow up.

  • +3 more secondary outcomes

Study Arms (1)

Prolonged Exposure therapy for posttraumatic stress disorder

EXPERIMENTAL

15 participants who meet study inclusion/exclusion criteria will be individually administered a full course of PE during 10, 60 minute-sessions, with independent multimodal assessment batteries administered at pre-treatment, mid-treatment (post session 5), post-treatment, and a 1-month follow-up.

Behavioral: Prolonged Exposure

Interventions

\- Participation will occur throughout 17 weeks over 15 separate visits during which 10, 60-minute sessions of PE will take place. Session 1 of PE will focus on psychoeducation. Session 2 of PE will involve a continuation of psychoeducation and rationale for exposure as well as the collaborative construction of the in vivo exposure hierarchy. After session 2, participants will begin homework where they are instructed to confront situations on their hierarchy. Starting in session 3 of PE, participants will begin imaginal exposures to their worst trauma memory. This involves the participant recounting and visualizing the trauma memory aloud with the clinician in the room for 30-40 minutes. The session will end with 15-20 minutes of processing the imaginal exposure. Participants will continue in-session imaginal exposures until the end of treatment. Throughout the treatment, participants will listen to a recording of their imaginal exposure and engage in in vivo exposures daily.

Prolonged Exposure therapy for posttraumatic stress disorder

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age 18 or older
  • Meeting diagnostic criteria for PTSD as defined by DSM-5 assessed by the Diagnostic Interview for Anxiety, Mood, and Obsessive-compulsive and related Psychiatric Disorders (DIAMOND), and
  • Interest in starting PE

You may not qualify if:

  • Current or past history of schizophrenic or other psychotic disorders,
  • Untreated Bipolar Disorder or a history of a manic/mixed episode within the last 6 months,
  • Severe traumatic brain injury,
  • Major neurological problems,
  • Current substance use disorder of moderate or greater severity assessed by the DIAMOND,
  • Active risk to self or others,
  • Current participation in therapy other than present-centered supportive therapy,
  • Previously received \> 2 sessions of Prolonged Exposure, and
  • Having no memory of their traumatic event.
  • For participants who are currently prescribed psychotropic medication, they will be eligible for the study provided medication use has been stable for 2 months prior to enrollment and remains stable throughout participation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

MGH

Boston, Massachusetts, 02114, United States

RECRUITING

Related Publications (40)

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MeSH Terms

Conditions

Stress Disorders, Post-Traumatic

Condition Hierarchy (Ancestors)

Stress Disorders, TraumaticTrauma and Stressor Related DisordersMental Disorders

Study Officials

  • Amanda W Baker, Ph.D.

    Massachusetts General Hospital

    PRINCIPAL INVESTIGATOR
  • Vladimir Ivkovic, Ph.D.

    Massachusetts General Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Amanda W Baker, Ph.D.

CONTACT

Vladimir Ivkovic, Ph.D.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

March 8, 2023

First Posted

March 28, 2023

Study Start

April 1, 2023

Primary Completion (Estimated)

March 1, 2027

Study Completion (Estimated)

December 1, 2027

Last Updated

November 13, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will share

A de-identified, anonymized dataset will be created and shared after study completion.

Shared Documents
STUDY PROTOCOL
Time Frame
Data will be available within a year of submission after publications.

Locations