Open Trial of Trauma-focused Psychodynamic Psychotherapy for People Living With HIV and PTSD (TFPP-PLWH)
Primary Purpose
Post Traumatic Stress Disorder, HIV
Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Trauma-focused psychodynamic psychotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Post Traumatic Stress Disorder focused on measuring PTSD, HIV, psychotherapy, trauma
Eligibility Criteria
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: Psychosis Bipolar I Acute suicidality Current substance use disorder Organic mental syndrome or intellectual disability Unstable non-HIV medical conditions
Sites / Locations
- Albert Einstein College of Medicine
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Trauma-focused psychodynamic psychotherapy
Arm Description
Twice-weekly psychotherapy for 24 sessions
Outcomes
Primary Outcome Measures
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.
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.
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.
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.
Secondary Outcome Measures
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.
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.
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.
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.
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.
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.
Change in symptom-specific reflective functioning
Lower scores indicate worse dysregulation, improvement denoted by higher numbers
Change in HIV Viral Load
Larger numbers are indicative of greater viral load and are worse
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)
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.
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
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.
Full Information
NCT ID
NCT05929911
First Posted
June 23, 2023
Last Updated
September 18, 2023
Sponsor
Montefiore Medical Center
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID)
1. Study Identification
Unique Protocol Identification Number
NCT05929911
Brief Title
Open Trial of Trauma-focused Psychodynamic Psychotherapy for People Living With HIV and PTSD
Acronym
TFPP-PLWH
Official Title
Pilot Feasibility Proposal to Adapt Trauma-focused Psychodynamic Psychotherapy (TFPP) for PLWH and PTSD
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 2023 (Anticipated)
Primary Completion Date
November 2024 (Anticipated)
Study Completion Date
November 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Montefiore Medical Center
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Traumatic Stress Disorder, HIV
Keywords
PTSD, HIV, psychotherapy, trauma
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Trauma-focused psychodynamic psychotherapy
Arm Type
Experimental
Arm Description
Twice-weekly psychotherapy for 24 sessions
Intervention Type
Behavioral
Intervention Name(s)
Trauma-focused psychodynamic psychotherapy
Other Intervention Name(s)
TFPP
Intervention Description
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.
Primary Outcome Measure Information:
Title
Change in PTSD Score based on the Clinician Administered PTSD Scale for DSM-5
Description
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
Title
Change in PTSD Score based on the Clinician Administered PTSD Scale for DSM-5
Description
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 5
Title
Change in PTSD Score based on the Clinician Administered PTSD Scale for DSM-5
Description
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)
Title
Change in PTSD Score based on the Clinician Administered PTSD Scale for DSM-5
Description
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 Outcome Measure Information:
Title
Change in Depression Score based on the Hamilton Depression Rating Scale (HDRS)
Description
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)
Title
Change in Anxiety Score based on the Hamilton Rating Scale for Anxiety (HAM-A)
Description
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)
Title
Change in Functional Impairment based on the Sheehan Disability Scale (SDS)
Description
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 5, Week 12 (treatment termination), 3-month post-treatment follow-up
Title
Change in Drug and/or Alcohol Problems based on the Short Inventory of Problems-Alcohol and Drugs (SIP-AD)
Description
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 5, Week 12 (treatment termination), 3-month post-treatment follow-up
Title
Change in Complex PTSD symptoms based on an International Trauma Interview
Description
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 5, Week 12 (treatment termination), 3-month post-treatment follow-up
Title
Attrition from treatment by end of therapy duration
Description
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)
Title
Change in symptom-specific reflective functioning
Description
Lower scores indicate worse dysregulation, improvement denoted by higher numbers
Time Frame
Baseline, Week 5, Week 12 (treatment termination)
Title
Change in HIV Viral Load
Description
Larger numbers are indicative of greater viral load and are worse
Time Frame
Baseline, Week 5, Week 12 (treatment termination)
Title
Change in AIDS Clinical Trials Group Adherence Questionnaire
Description
Gives a 3D day for day measure of AIDS drug compliance. Bigger number are better (taking more doses of medicine)
Time Frame
Baseline, Week 5, Week 12 (treatment termination), 3-month post-treatment follow-up
Title
Change in salivary cortisol
Description
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
Title
Change in salivary cytokines
Description
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
Title
Number of patients with clinical PTSD response based on the Clinician Administered PTSD Scale for DSM-5
Description
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 5, Week 12 (treatment termination), 3-month post-treatment follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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:
Psychosis
Bipolar I
Acute suicidality
Current substance use disorder
Organic mental syndrome or intellectual disability
Unstable non-HIV medical conditions
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
John R Keefe, PhD
Phone
703-981-7184
Email
john.keefe@einsteinmed.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Barbara L Milrod, MD
Phone
917-593-1377
Email
bmilrod@montefiore.edu
Facility Information:
Facility Name
Albert Einstein College of Medicine
City
Bronx
State/Province
New York
ZIP/Postal Code
10461
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John R Keefe, PhD
Phone
347-391-4189
Email
john.keefe@einsteinmed.edu
First Name & Middle Initial & Last Name & Degree
Barbara L Milrod, MD
Email
bmilrod@montefiore.org
First Name & Middle Initial & Last Name & Degree
Barbara L Milrod, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Open Trial of Trauma-focused Psychodynamic Psychotherapy for People Living With HIV and PTSD
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