Purpose

This is a randomized controlled trial of Trauma-Focused Psychodynamic Psychotherapy (TFPP) in comparison with TAU (at the VA) in a 2:1 ratio in 75 Veterans with PTSD who have not responded to standard treatment at the VA.

Condition

Eligibility

Eligible Ages
Between 18 Years and 70 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Reporting moderate PTSD, as defined by a CAPS score of >40 - Have at least one of the following history with CPT and/or PE: - offered and declined - dropped out of treatment - been determined unsuitable by their treatment team - received treatment but continue to experience symptoms meeting entrance criteria. - Require stabilization on psychiatric medication for 2 month period prior to entry into study to avoid confounding treatments

Exclusion Criteria

  • Presence of SCID-5 assessed psychotic disorder, bipolar disorder, or substance use that would interfere with trial demands - Severe suicidality that would require immediate crisis management - Organic mental syndromes, delirium, or unstable medical conditions that would interfere with trial demands - Inability to meet trial demands.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Intervention Model Description
Randomized controlled trial of psychosocial interventions
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)
Masking Description
All assessments will be performed by blinded clinical assessors; randomization accomplished by computer algorhythm

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
TFPP
TFPP is a manualized 16-24 session psychodynamic psychotherapy targeted on trauma symptoms of PTSD
  • Other: TFPP
    Trauma-Focused Psychodynamic Psychotherapy
    Other names:
    • psychodynamic psychotherapy
Active Comparator
TAU
TAU in this study is treatment for PTSD as currently delivered at the VA
  • Other: TAU
    treatment as usual at the VA for PTSD

Recruiting Locations

More Details

Status
Recruiting
Sponsor
Montefiore Medical Center

Study Contact

Emily Villeveuve
(212) 686-7500
Emily.Villeneuve@va.gov

Detailed Description

Veterans with PTSD are a highly vulnerable population with tremendous disability and unmet needs. Few VA patients with PTSD now actually receive evidence-based psychotherapy because current exposure-based treatments have low uptake. The project goal is to expand the range of PTSD psychotherapy treatments available at Veterans Administration Medical Centers. This pilot trauma recovery proposal takes the next step in translating a brief efficacious psychotherapy developed and tested for panic disorder, Panic Focused Psychodynamic Psychotherapy (PFPP) for Veterans with PTSD at the VA New York Harbor Healthcare System (VA NYHHCS). PFPP was developed, manualized, and studied in RCTs over the past two decades. We hope that Trauma-Focused Psychodynamic Psychotherapy (TFPP), an adaptation of PFPP, with its high response rates in panic disorder with/without agoraphobia, and non-exposure protocol, will fill crucial gaps in Veteran care. A major challenge facing psychotherapy research is translating and implementing efficacious therapies to the community. No psychodynamic psychotherapy for anxiety or PTSD has achieved this in the US. This pilot RCT represents a paradigm shift in its approach to trauma. TFPP will be the only PTSD treatment for Veterans to incorporate Veterans' input into refinement of the treatment as this project progresses. TFPP targets aspects of traumatic experience and approaches Veterans' lives more broadly than the symptom-focused treatments the VA currently offers our traumatized Veterans.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.