RECRUITING

Post-Traumatic Stress Disorder Focused Psychodynamic Psychotherapy

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PTSDpsychotherapypsychodynamic psychotherapy

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

A Pilot Randomized Controlled Trial of Trauma-Focused Psychodynamic Psychotherapy (TFPP) at the VA in Veterans With PTSD

Quick Facts

Study Start:2018-11-02
Study Completion:2026-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03755401

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 70 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Reporting moderate PTSD, as defined by a CAPS score of \>40
  2. * Have at least one of the following history with CPT and/or PE:
  3. * offered and declined
  4. * dropped out of treatment
  5. * been determined unsuitable by their treatment team
  6. * received treatment but continue to experience symptoms meeting entrance criteria.
  7. * Require stabilization on psychiatric medication for 2 month period prior to entry into study to avoid confounding treatments
  1. * Presence of SCID-5 assessed psychotic disorder, bipolar disorder, or substance use that would interfere with trial demands
  2. * Severe suicidality that would require immediate crisis management
  3. * Organic mental syndromes, delirium, or unstable medical conditions that would interfere with trial demands
  4. * Inability to meet trial demands.

Contacts and Locations

Study Contact

Emily Villeveuve
CONTACT
(212) 686-7500
Emily.Villeneuve@va.gov
Cory K Chen, Ph.D.
CONTACT
(212) 686-7500
Cory.Chen@va.gov

Principal Investigator

Barbara Milrod, MD
PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University

Study Locations (Sites)

VA New York Harbor Healthcare System - Manhattan Campus
New York, New York, 10010
United States

Collaborators and Investigators

Sponsor: Montefiore Medical Center

  • Barbara Milrod, MD, PRINCIPAL_INVESTIGATOR, Weill Medical College of Cornell University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2018-11-02
Study Completion Date2026-05

Study Record Updates

Study Start Date2018-11-02
Study Completion Date2026-05

Terms related to this study

Keywords Provided by Researchers

  • psychotherapy
  • psychodynamic psychotherapy

Additional Relevant MeSH Terms

  • PTSD