Open Trial of Trauma-focused Psychodynamic Psychotherapy for People Living With HIV and PTSD
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorMontefiore Medical Center
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
Psychosis
Bipolar I
Acute suicidality
Current substance use disorder
Trial design
Design model
Single group
Treatments tested in this trial
Trauma-focused psychodynamic psychotherapy
BehavioralThis 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.
Treatment groups
20 Participants
are divided into 1 treatment groupGroup A: Trauma-focused psychodynamic psychotherapyExperimental treatment 1 intervention
Trial outcomes
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
Baseline2
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 63
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-upSecondary 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-upOther 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-up2
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-up4
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-upSponsors and contacts
Click on the lead sponsor to view all of their trials.
Montefiore Medical Center
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborator
American Psychoanalytic Association (APsA)
Collaborator
Source ClinicalTrials.gov