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RecruitingNCT05929911TFPP-PLWHUpdated Jun 12, 2026

Open Trial of Trauma-focused Psychodynamic Psychotherapy for People Living With HIV and PTSD

An interventional study of Trauma-focused psychodynamic psychotherapy in Post Traumatic Stress Disorder (PTSD) and HIV, sponsored by Montefiore Medical Center. Recruiting at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-06-12.

Sponsored by Montefiore Medical Center · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Apr 2024; still recruiting 2 years 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
01

Study summary

People living with HIV (PLWH) have a higher rate of post-traumatic stress disorder (PTSD) diagnosis than the general population. Comorbid PTSD is also associated with negative HIV-related health outcomes. Unfortunately, little outcome research has examined the usefulness of PTSD treatments for PTSD. This pilot study adapts for PLWH a non-exposure based psychotherapy for PTSD focused on reflecting on one's emotions and relationships and understanding and working through how trauma may have disrupted them. The study team is interested in better understanding the needs of PLWH with PTSD, learning whether PLWH with PTSD find this treatment acceptable and helpful, and beginning to understand the relationship between HIV-related health factors (e.g., inflammation and stress biology) and PTSD, and how these health factors may improve during treatment.

02

Conditions studied

  • Post Traumatic Stress Disorder (PTSD)
  • HIV

Keywords

  • HIV
  • psychotherapy
  • trauma
03

In context

Stress Disorders, Post-Traumatic

2,239 studies on the registry are indexed under Stress Disorders, Post-Traumatic; 554 are open to participants now.

This study's planned enrollment of 20 is below the median of 70 across 1,858 interventional studies indexed under Stress Disorders, Post-Traumatic.

Browse Stress Disorders, Post-Traumatic studies →

Lead sponsor

Montefiore Medical Center is the lead sponsor of 402 studies on the registry; 70 are open to participants now.

Of its 81 completed or terminated interventional studies of FDA-regulated products, 73 (90%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Diagnosis of DSM-5 defined PTSD, per the Clinician Administered PTSD Scale \& CAPS-5 total severity score greater than or equal to 25
  • HIV diagnosis (by medical records or HIV testing)
  • Stable psychiatric/psychotropic medication for >=2 months and ongoing during treatment

Exclusion criteria

Exclusion Criteria:

  • Psychosis
  • Bipolar I
  • Acute suicidality
  • Current substance use disorder
  • Organic mental syndrome or intellectual disability
  • Unstable non-HIV medical conditions
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    Trauma-focused psychodynamic psychotherapy

    Twice-weekly psychotherapy for 24 sessions

    Behavioral: Trauma-focused psychodynamic psychotherapy

Interventions

  • BehavioralTrauma-focused psychodynamic psychotherapy

    This psychotherapy addresses disruptions in the ability to reflect and affective regulation by exploring the psychological meanings of symptoms and their relation to traumatic events. The therapist works to identify intrapsychic conflicts, intense negative affects, and defense mechanisms related to the PTSD syndrome using a psychodynamic formulation that provides a framework for intervention. The transference provides a forum for patients to address feelings of mistrust, difficulties with authority, fears of abuse, angry and guilty feelings, and fantasies. This treatment will be provided in-person or over teletherapy as the public health situation demands.

    Also known as: TFPP

06

What researchers measure

Primary outcomes

  1. Change in PTSD Score based on the Clinician Administered PTSD Scale for DSM-5

    Lower scores denote less severe PTSD symptoms; a decline of at least 30% from an individual's baseline CAPS score is defined as a treatment response on the CAPS; diagnostic remission will be defined as achieving response plus failing to meet for DSM-5 defined PTSD per the CAPS after treatment.

    Time frame: Baseline

  2. Change in PTSD Score based on the Clinician Administered PTSD Scale for DSM-5

    Lower scores denote less severe PTSD symptoms; a decline of at least 30% from an individual's baseline CAPS score is defined as a treatment response on the CAPS; diagnostic remission will be defined as achieving response plus failing to meet for DSM-5 defined PTSD per the CAPS after treatment.

    Time frame: Week 6

  3. Change in PTSD Score based on the Clinician Administered PTSD Scale for DSM-5

    Lower scores denote less severe PTSD symptoms; a decline of at least 30% from an individual's baseline CAPS score is defined as a treatment response on the CAPS; diagnostic remission will be defined as achieving response plus failing to meet for DSM-5 defined PTSD per the CAPS after treatment.

    Time frame: Week 12 (treatment termination)

  4. Change in PTSD Score based on the Clinician Administered PTSD Scale for DSM-5

    Lower scores denote less severe PTSD symptoms; a decline of at least 30% from an individual's baseline CAPS score is defined as a treatment response on the CAPS; diagnostic remission will be defined as achieving response plus failing to meet for DSM-5 defined PTSD per the CAPS after treatment.

    Time frame: 3-month post-treatment follow-up

Secondary outcomes

  1. Change in Depression Score based on the Hamilton Depression Rating Scale (HDRS)

    The HDRS (also known as the Ham-D) scale contains 17 items pertaining to symptoms of depression experienced over the past week. Scoring is based on the 17-item scale and scores of 0-7 are considered as being normal, 8-16 suggest mild depression, 17-23 moderate depression, and scores over 24 are indicative of severe depression with the maximum score being 52 on the 17-point scale.

    Time frame: Baseline, Week 12 (treatment termination)

  2. Change in Anxiety Score based on the Hamilton Rating Scale for Anxiety (HAM-A)

    Severity of anxiety will be assessed using the Hamilton Rating Scale for Anxiety (HAM-A). The scale consists of 14 items, each defined by a series of symptoms, and measures both psychic anxiety (mental agitation and psychological distress) and somatic anxiety (physical complaints related to anxiety). Each item is scored on a scale of 0 (not present) to 4 (severe), with a total score range of 0-56, where \<17 indicates mild severity, 18-24 mild to moderate severity and 25-30 moderate to severe anxiety.

    Time frame: Baseline, Week 12 (treatment termination)

  3. Change in Functional Impairment based on the Sheehan Disability Scale (SDS)

    The Sheehan Disability Scale is a composite of three self-rated items designed to measure the extent to which three major domains in the patient's life are functionally impaired by psychiatric or medical symptoms. The SDS is a brief, 5-item self-report tool that assesses functional impairment in work/school (0-10 scoring range), social life (0-10 scoring range), and family life (0-10 scoring range). A composite range of 0-30 is possible. Scores of ≥5 on any of the 3 individual scales and overall higher totals scores are associated with significant functional impairment.

    Time frame: Baseline, Week 6, Week 12 (treatment termination), 3-month post-treatment follow-up

Other outcomes

  1. Change in Drug and/or Alcohol Problems based on the Short Inventory of Problems-Alcohol and Drugs (SIP-AD)

    The Short Inventory of Problems Alcohol and Drugs is a fifteen item instrument used to assess the self-reported consequences of alcohol and substance abuse. The format establishes whether consequences ever happened to the respondents and the frequency of occurrence of the consequences. Possible responses are scored on a 4-point scale (0 = Never; 1 = Once or a few times; 2 = Once or twice a week; 3 = Daily or almost daily) based on occurrences over the prior 3-month period. A higher composite total is indicative of increasingly severe consequences.

    Time frame: Baseline, Week 6, Week 12 (treatment termination), 3-month post-treatment follow-up

  2. Attrition from treatment by end of therapy duration

    Attrition from treatment will be evaluated by the failure to complete experimental psychotherapy intervention defined as attending at least 16 out of 24 TFPP sessions within the 12-week period OR patient declaring intention to not attend any further TFPP sessions during the 12-week period. The specific session in which the patient dropped out will be recorded.

    Time frame: Up to Treatment Termination (Week 12)

  3. Change in AIDS Clinical Trials Group Adherence Questionnaire

    Gives a 3D day for day measure of AIDS drug compliance. Bigger number are better (taking more doses of medicine)

    Time frame: Baseline, Week 6, Week 12 (treatment termination), 3-month post-treatment follow-up

  4. Number of patients with clinical PTSD response based on the Clinician Administered PTSD Scale for DSM-5

    Lower scores denote less severe PTSD symptoms; a decline of at least 30% from an individual's baseline CAPS score is defined as a treatment response on the CAPS; diagnostic remission will be defined as achieving response plus failing to meet for DSM-5 defined PTSD per the CAPS after treatment.

    Time frame: Baseline, Week 6, Week 12 (treatment termination), 3-month post-treatment follow-up

  5. Change in salivary cytokines

    Multiple cytokines will be assessed: 14-Plex Luminex Panel of cytokines IL-1α, IL-1β, IL-6, IL-8, IL-17, TNF, IFN-g, MCP-1, MIP-3α, MIP-1α, MIP-1β, RANTES, GMCSF and CXCL9. Interpretation is joint, complicated, and determined within subject

    Time frame: Baseline, Week 12 (treatment termination), 3-month post-treatment follow-up

  6. Change in salivary cortisol

    normal morning cortisol level depends on the lab but is around 0.094-1.551 µg/dL. Interpretations are made with-in person.

    Time frame: Baseline, Week 12 (treatment termination), 3-month post-treatment follow-up

  7. Change in HIV Viral Load

    Larger numbers are indicative of greater viral load and are worse

    Time frame: Baseline, Week 6, Week 12 (treatment termination)

  8. Change in Complex PTSD symptoms based on an International Trauma Interview

    Additional instrument based off of the CAPS-5, assessing ICD-11 defined Complex PTSD symptoms; additionally meeting for Complex PTSD is defined by having at least one clinically significant symptom in each of the 3 symptom domains.

    Time frame: Baseline, Week 6, Week 12 (treatment termination), 3-month post-treatment follow-up

  9. Change in symptom-specific reflective functioning

    Lower scores indicate worse dysregulation, improvement denoted by higher numbers

    Time frame: Baseline, Week 6, Week 12 (treatment termination)

07

Study locations

1 of 1 sites recruiting
  • Albert Einstein College of Medicine
    The Bronx, New York 10461, United States
    Recruiting
08

References and documents

Publications

  • Kehn M, Milrod B, Chen CK. Clinical Case of Trauma-Focused Psychodynamic Psychotherapy for a Veteran With PTSD and Race-Based Trauma. Am J Psychother. 2024 Sep 1;77(3):146-150. doi: 10.1176/appi.psychotherapy.20230040. No abstract available. PubMed 39277802 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05929911
Lead sponsor
Montefiore Medical Center
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID), American Psychoanalytic Association (APsA)
Responsible party
Sponsor
First posted
Jul 3, 2023
Start date
Apr 26, 2024
Primary completion
Jun 2027 (estimated)
Completion
Jun 2027 (estimated)
Last update
Jun 12, 2026

Study contacts

John R Keefe, PhD
Contact
john.keefe@einsteinmed.edu
703-981-7184
Barbara L Milrod, MD
Contact
bmilrod@montefiore.edu
917-593-1377
Barbara Milrod, MD
principal investigator · Montefiore Medical Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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