Post-Traumatic Stress Disorder
Conditions
Brief summary
VA Cooperative Study CSP #591 is designed to compare the effectiveness of two types of psychotherapy, Prolonged Exposure (PE) and Cognitive Processing Therapy (CPT), for treating posttraumatic stress disorder (PTSD) in male and female Veterans. Despite solid evidence that both treatments are effective in Veterans and non-Veterans, there is a lack of evidence about the effectiveness of these treatments compared with one another. The sample will include 900 male and female Veterans with PTSD due to any traumatic military event. Veterans who are eligible and agree to participate in the study will be randomly assigned (by chance) to receive Prolonged Exposure or Cognitive Processing Therapy. The standard dose of treatment is 12 weekly sessions but Veterans who improve more rapidly may finish in fewer sessions and Veterans who improve more slowly may have additional sessions. The primary outcome is improvement in PTSD symptoms after treatment. The outcome will be measured at regular follow-up visits that will occur at the middle and at the end of treatment and then 3 and 6 months later. The investigators will measure other outcomes, including additional mental health problems, functioning, quality of life, and use of treatments for mental and physical problems. The investigators also will measure Veterans' treatment preference and examine whether Veterans who get the treatment they prefer do better than Veterans who get the less-preferred treatment. As a large multi-site trial with men and women, CSP #591 is designed to provide conclusive information about whether one treatment is better than the other, overall and for different types of patients-for example, men vs. women, combat Veterans vs. Veterans who experienced military sexual trauma, and older vs. younger Veterans. Regardless of the outcome, patients will have more information to help them make an informed decisions about which treatment to choose and VA will have stronger evidence to help make care Veteran-centered.
Detailed description
VA Cooperative Study CSP #591 is designed to compare the effectiveness of Prolonged Exposure (PE) and Cognitive Processing Therapy (CPT) for treating posttraumatic stress disorder (PTSD) in male and female Veterans. PTSD is a serious and prevalent condition in Veterans, affecting just under 9% of VA patients in Fiscal Year 2011 (FY11). Since 2005, the number of VA patients with PTSD has increased 14.8% annually, due not only to new Veterans but also to increased numbers of Vietnam Veterans who are seeking care. In FY11, PTSD was the 3rd most common service-connected disability in VA. Despite solid evidence that Prolonged Exposure and Cognitive Processing Therapy are effective treatments for PTSD in Veterans and non-Veterans, there is insufficient evidence about the effectiveness of these treatments relative to one another. The only study to compare the treatments, a single-site trial in non-Veteran female rape survivors, failed to find a difference, but the study was not adequately powered to compare two such effective treatments. Other data are similarly inconclusive. CSP #591 would break new ground as the first large-scale comparative effectiveness trial of treatment for PTSD and the first study to provide definitive information about how effective treatments for PTSD compare with one another. The study will be a prospective randomized clinical trial with blinded assessment. The population will be male and female Veterans with PTSD due to any traumatic military event. Patients who are eligible and agree to participate in the study will be randomly assigned in a 1:1 ratio to receive Prolonged Exposure or Cognitive Processing Therapy. The investigators propose to administer 12 weekly sessions of each treatment as a standard dose but to allow participants who improve more rapidly to finish in 10 or 11 sessions and participants who have not attained adequate improvement by session 12 to have up to 2 additional sessions. The primary outcome is improvement in PTSD symptom severity as measured by change on the Clinician-Administered PTSD Scale after treatment. The outcome measure will be determined from regular follow-up visits of the patients, which will occur at the middle and at the end of treatment and then 3 and 6 months later. Secondary outcomes include other measures of PTSD, comorbid mental health problems, functioning, quality of life, and service utilization. The investigators also will measure participants' treatment preference and examine whether concordance between preference and allocation is associated with increased treatment effectiveness. In order to detect a standardized mean difference in improvement in PTSD symptom severity of d = .25, a sample size of 900 randomized patients provides 90% power to detect a difference between arms using the linear mixed effects model with a two-sided = .05. Given the lack of conclusive findings to predict which treatment is better, the investigators propose to test a nondirectional hypothesis. Assuming 2.5 years of accrual and an enrollment of 26 participants per year at each site, the investigators would need 14.1 sites to enroll a total of 64 participants per site. The investigators propose to recruit 17 sites to guard against the possibility that some sites will not enroll the required number of participants. VA has a vested interest in understanding the relative effectiveness of Prolonged Exposure and Cognitive Processing Therapy. Both treatments are recommended at the highest level in the Veterans Affairs (VA)/Department of Defense (DoD) PTSD Practice Guideline. VA is required to make these treatments available to Veterans seeking PTSD care. The treatments are being disseminated nationally across the VA system in order to enhance the availability of evidence-based treatments to Veterans with PTSD. VA also has developed a national PTSD Mentoring Program for PTSD Program Administrators to help them manage their clinics to permit the delivery of these treatments. Every facility has an evidence-based therapy coordinator as well to facilitate training in evidence-based psychotherapy. As a large multi-site trial with men and women, CSP #591 would provide definitive information about the comparative effectiveness of Prolonged Exposure and Cognitive Processing Therapy and maximize the study's impact on the field. Because the treatments are based on differing theories about the development of PTSD, a demonstration that one treatment is superior to the other would further scientific exploration by challenging theoretical accounts of etiology and treatment. Regardless of which treatment is better, patients would have more information to help them make an informed decision about which treatment to choose and VA would have stronger evidence to help make care Veteran-centered.
Interventions
CPT consists of cognitive therapy and a written trauma narrative. Patients are taught to challenge their beliefs through Socratic questioning and the use of daily worksheets. The initial focus is on beliefs such as denial and self-blame, and then shifts to overgeneralized beliefs about self and the world. Patients process their trauma directly by writing a narrative of their traumatic event(s) that they read to themselves and to therapists. The typical protocol consists of 12 1-hr sessions. In this study, the 12-session protocol will be followed, but participants who improve more rapidly may finish in 10 sessions and those who improve more slowly may receive up to 2 additional sessions to continue working on stuck points with challenging beliefs worksheets.
PE is a manualized, 90-minute, 8-15 week treatment program based on emotional processing theory, which posits that anxiety disorders, including PTSD, reflect pathological fear structures in which emotional and cognitive associations among different elements do not accurately represent reality and renders the individual dysfunctional and distressed. PE is designed to correct erroneous connections in the targeted memory structure. PTSD sufferers typically experience two key pathological emotional response sets and related cognitions: The world is an utterly dangerous place, and I am completely incompetent and unable to cope with stress. In this study, the 12-session protocol will be followed, but participants improve more rapidly may finish in 10 sessions and those who improve more slowly may have up to 2 additional sessions to continue working on exposure.
Sponsors
Study design
Eligibility
Inclusion criteria
Current PTSD and symptom severity of 25 or higher on the Clinician- Administered PTSD Scale (Weathers et al., 2013); agreement to not receive psychotherapy for PTSD during study treatment and allow digital recording of phone interviews and therapy; regular access to a telephone (or agreement to come to the VA for centrally conducted telephone interviews for participant who do not have telephone access). Medication for PTSD and other mental or physical conditions, psychotherapy for other problems, brief visits with an existing therapist, and self-help groups will be allowed.
Exclusion criteria
* substance dependence not in remission for at least 1 month; * current psychotic symptoms and mania (including manic phase of bipolar disorder); * significant current suicidal or homicidal ideation that includes a specific plan; * or moderate to severe cognitive impairment defined as 1 SD below age-graded norms on the Montreal Cognitive Assessment.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS) | immediate post-treatment, 3 and 6 months | The primary outcome is the change of CAPS-5 total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). We chose to use the average in the six months post-treatment in the definition of primary outcome (versus using a single post-treatment timepoint) because we anticipate that improvement established during the course of treatment will be sustained in the 6 months after treatment for both PE and CPT. Possible range for CAPS-5 total score 0-80. Higher score indicates more severe PTSD. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Beck Depression Inventory-II (BDI-II) | immediate post-treatment, 3 and 6 months | BDI-II is a brief, self-report inventory designed to measure the severity of depression symptomatology. The outcome is the change of BDI-II total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for BDI-II 0-63. Higher score indicates more severe depressive symptoms (0-13 minimal, 14-29 mild, 20-28 moderate, 29-63 severe). |
| Spielberger State Anger Inventory (STAXI) | immediate post-treatment, 3 and 6 months | The STAXI is a commonly used measure of trait and state anxiety. The outcome is the change of STAI total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for STAXI 44-176. Higher score indicates greater intensity of anger. |
| Short Inventory of Problems - Revised (SIP-R) | immediate post-treatment, 3 and 6 months | The SIP-R assesses alcohol-related consequences. The outcome is the change of SIP-R total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for SIP-R 0-51. Higher score indicates more severe adverse consequences of substance use. |
| Posttraumatic Diagnostic Scale (PDS-5) | immediate post-treatment, 3 and 6 months | The PDS-5 is a 24-item self-report measure that assesses PTSD symptom severity in the last month according to DSM-5 criteria. The outcome is the change of PDS-5 total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for PDS-5 score 0-80. Higher PDS-5 Score indicates more severe PTSD Symptoms. |
| World Health Organization Disability Assessment Schedule (WHO-DAS-II) | immediate post-treatment, 3 and 6 months | The WHO-DAS-II is an assessment instrument for health and disability. The outcome is the change of WHO-DAS-II total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for WHODAS-II 12-60. Higher score indicates more difficulty and disability due to health condition. |
| World Health Organization Quality of Life (WHOQoL-BREF) | immediate post-treatment, 3 and 6 months | The WHOQoL-BREF is a quality of life assessment. The outcome is the change of WHOQoL-BREF assessment sub-category (Physical Health, Psychological, Social Relationships, Environment) scores from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for WHOQOL-BREF 0-100, Physical Health 0-100, Psychological 0-100, Social Relationships 0-100, and Environment 0-100. Higher score indicates better satisfaction with life. |
| Brief Addiction Monitor (BAM) | immediate post-treatment, 3 and 6 months | The BAM measures an individual's health, alcohol, and drug use. The outcome is the change of BAM total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Range: 0-4 points. Higher score indicates worse outcome (i.e., more severe addiction). |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Behavioral: Prolonged Exposure (PE) PE is a manualized, 90-minute, 8-15 week treatment program based on emotional processing theory, which posits that anxiety disorders, including PTSD, reflect pathological fear structures in which emotional and cognitive associations among different elements do not accurately represent reality and renders the individual dysfunctional and distressed. PE is designed to correct erroneous connections in the targeted memory structure. PTSD sufferers typically experience two key pathological emotional response sets and related cognitions: The world is an utterly dangerous place, and I am completely incompetent and unable to cope with stress. In this study, the 12-session protocol will be followed, but participants improve more rapidly may finish in 10 sessions and those who improve more slowly may have up to 2 additional sessions to continue working on exposure. | 455 |
| Behavioral: Cognitive Processing Therapy (CPT) CPT consists of cognitive therapy and a written trauma narrative. Patients are taught to challenge their beliefs through Socratic questioning and the use of daily worksheets. The initial focus is on beliefs such as denial and self-blame, and then shifts to overgeneralized beliefs about self and the world. Patients process their trauma directly by writing a narrative of their traumatic event(s) that they read to themselves and to therapists. The typical protocol consists of 12 1-hr sessions. In this study, the 12-session protocol will be followed, but participants who improve more rapidly may finish in 10 sessions and those who improve more slowly may receive up to 2 additional sessions to continue working on stuck points with challenging beliefs worksheets. | 461 |
| Total | 916 |
Baseline characteristics
| Characteristic | Behavioral: Cognitive Processing Therapy (CPT) | Total | Behavioral: Prolonged Exposure (PE) |
|---|---|---|---|
| Age, Continuous | 44.9 years | 45.2 years | 45.5 years |
| Any current comorbid psychiatric disorder Anxiety disorder | 166 Participants | 305 Participants | 139 Participants |
| Any current comorbid psychiatric disorder Mood disorder | 332 Participants | 641 Participants | 309 Participants |
| Any current comorbid psychiatric disorder Obsessive compulsive disorder | 29 Participants | 48 Participants | 19 Participants |
| Any current comorbid psychiatric disorder Substance use disorders | 40 Participants | 72 Participants | 32 Participants |
| Any current comorbid psychiatric disorder | 371 Participants | 714 Participants | 343 Participants |
| Any lifetime comorbid psychiatric disorder Anxiety disorder | 181 Participants | 330 Participants | 149 Participants |
| Any lifetime comorbid psychiatric disorder Mood disorder | 400 Participants | 798 Participants | 398 Participants |
| Any lifetime comorbid psychiatric disorder Obsessive compulsive disorder | 36 Participants | 60 Participants | 24 Participants |
| Any lifetime comorbid psychiatric disorder Substance use disorders | 112 Participants | 242 Participants | 130 Participants |
| Any lifetime comorbid psychiatric disorder | 424 Participants | 841 Participants | 417 Participants |
| Beck Depression Inventory-II | 30.0 score on a scale | 30.2 score on a scale | 30.3 score on a scale |
| Beck Depression Inventory-II Suicidality (BDI-II Item 9) | 156 Participants | 319 Participants | 163 Participants |
| Brief Addiction Monitor | 0.8 score on a scale | 0.8 score on a scale | 0.8 score on a scale |
| Clinician Administered PTSD Scale-5 | 40.3 score on a scale | 40.1 score on a scale | 39.9 score on a scale |
| Ethnicity: Spanish, Hispanic or Latino | 72 Participants | 139 Participants | 67 Participants |
| Lifetime trauma exposure Any sexual trauma | 163 Participants | 329 Participants | 166 Participants |
| Lifetime trauma exposure Combat exposure | 347 Participants | 704 Participants | 357 Participants |
| Lifetime trauma exposure Disaster exposure | 385 Participants | 776 Participants | 391 Participants |
| Lifetime trauma exposure Life-threatening illness or injury | 163 Participants | 317 Participants | 154 Participants |
| Lifetime trauma exposure Other traumatic event | 354 Participants | 725 Participants | 371 Participants |
| Lifetime trauma exposure Physical assault | 408 Participants | 794 Participants | 386 Participants |
| Lifetime trauma exposure Serious accident | 389 Participants | 774 Participants | 385 Participants |
| Lifetime trauma exposure: Number of event types (of 17) | 7.4 number of event types | 7.54 number of event types | 7.7 number of event types |
| Married/cohabitating | 237 Participants | 483 Participants | 246 Participants |
| Number of patients preferring PE treatment at baseline | 214 Participants | 446 Participants | 232 Participants |
| Positive VA Military Sexual Trauma Screen | 133 Participants | 267 Participants | 134 Participants |
| Positive VA Traumatic Brain Injury Screen | 281 Participants | 575 Participants | 294 Participants |
| Post-high school education | 192 Participants | 408 Participants | 216 Participants |
| Posttraumatic Diagnostic Scale | 50.5 score on a scale | 50.63 score on a scale | 50.7 score on a scale |
| PTSD disability Approved | 202 Participants | 388 Participants | 186 Participants |
| PTSD disability Denied | 19 Participants | 45 Participants | 26 Participants |
| PTSD disability Never applied | 109 Participants | 234 Participants | 125 Participants |
| PTSD disability Pending | 129 Participants | 245 Participants | 116 Participants |
| Race/Ethnicity, Customized American Indian/Alaskan Native | 15 Participants | 33 Participants | 18 Participants |
| Race/Ethnicity, Customized Asian | 11 Participants | 25 Participants | 14 Participants |
| Race/Ethnicity, Customized Black | 130 Participants | 249 Participants | 119 Participants |
| Race/Ethnicity, Customized Native Hawaiian/Pacific Islander | 10 Participants | 17 Participants | 7 Participants |
| Race/Ethnicity, Customized Other | 25 Participants | 46 Participants | 21 Participants |
| Race/Ethnicity, Customized White | 289 Participants | 590 Participants | 301 Participants |
| Receiving psychotherapy | 98 Participants | 193 Participants | 95 Participants |
| Service Era Gulf War | 87 Participants | 172 Participants | 85 Participants |
| Service Era OEF/OIF/OND | 270 Participants | 530 Participants | 260 Participants |
| Service Era Other | 59 Participants | 125 Participants | 66 Participants |
| Service Era Vietnam | 77 Participants | 159 Participants | 82 Participants |
| Sex: Female, Male Female | 92 Participants | 186 Participants | 94 Participants |
| Sex: Female, Male Male | 369 Participants | 730 Participants | 361 Participants |
| Short Inventory of Problems-Revised | 3.3 score on a scale | 3.4 score on a scale | 3.5 score on a scale |
| Spielberger Trait Anger Expression Inventory Anger Expression | 36.4 score on a scale | 36.9 score on a scale | 37.3 score on a scale |
| Spielberger Trait Anger Expression Inventory State Anger | 17.9 score on a scale | 17.9 score on a scale | 17.8 score on a scale |
| Spielberger Trait Anger Expression Inventory Trait Anger | 24.2 score on a scale | 24.2 score on a scale | 24.1 score on a scale |
| Taking psychotropic medication | 317 Participants | 620 Participants | 303 Participants |
| Unemployed | 263 Participants | 534 Participants | 271 Participants |
| World Health Organization Disability Adjustment Scale-II | 29.7 score on a scale | 29.6 score on a scale | 29.4 score on a scale |
| World Health Organization Quality of Life-BREF Environment | 57.4 score on a scale | 57.8 score on a scale | 58.2 score on a scale |
| World Health Organization Quality of Life-BREF Physical Health | 43.7 score on a scale | 44.1 score on a scale | 44.4 score on a scale |
| World Health Organization Quality of Life-BREF Psychological | 46.4 score on a scale | 46.5 score on a scale | 46.5 score on a scale |
| World Health Organization Quality of Life-BREF Social Relationships | 40.6 score on a scale | 41.0 score on a scale | 41.3 score on a scale |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 1 / 455 | 2 / 461 |
| other Total, other adverse events | 42 / 455 | 65 / 461 |
| serious Total, serious adverse events | 55 / 455 | 63 / 461 |
Outcome results
Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS)
The primary outcome is the change of CAPS-5 total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). We chose to use the average in the six months post-treatment in the definition of primary outcome (versus using a single post-treatment timepoint) because we anticipate that improvement established during the course of treatment will be sustained in the 6 months after treatment for both PE and CPT. Possible range for CAPS-5 total score 0-80. Higher score indicates more severe PTSD.
Time frame: immediate post-treatment, 3 and 6 months
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| Behavioral: Prolonged Exposure (PE) | Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS) | Posttreatment | 24.3 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS) | 3 Months | 26.4 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS) | 6 Months | 24.8 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS) | Posttreatment | 27.2 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS) | 3 Months | 28.7 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS) | 6 Months | 26.9 score on a scale |
Beck Depression Inventory-II (BDI-II)
BDI-II is a brief, self-report inventory designed to measure the severity of depression symptomatology. The outcome is the change of BDI-II total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for BDI-II 0-63. Higher score indicates more severe depressive symptoms (0-13 minimal, 14-29 mild, 20-28 moderate, 29-63 severe).
Time frame: immediate post-treatment, 3 and 6 months
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| Behavioral: Prolonged Exposure (PE) | Beck Depression Inventory-II (BDI-II) | Posttreatment | 22.0 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Beck Depression Inventory-II (BDI-II) | 3 Months | 22.2 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Beck Depression Inventory-II (BDI-II) | 6 Months | 21.9 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Beck Depression Inventory-II (BDI-II) | Posttreatment | 22.7 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Beck Depression Inventory-II (BDI-II) | 3 Months | 23.6 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Beck Depression Inventory-II (BDI-II) | 6 Months | 22.9 score on a scale |
Brief Addiction Monitor (BAM)
The BAM measures an individual's health, alcohol, and drug use. The outcome is the change of BAM total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Range: 0-4 points. Higher score indicates worse outcome (i.e., more severe addiction).
Time frame: immediate post-treatment, 3 and 6 months
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| Behavioral: Prolonged Exposure (PE) | Brief Addiction Monitor (BAM) | Posttreatment | 0.88 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Brief Addiction Monitor (BAM) | 3 Months | 1.0 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Brief Addiction Monitor (BAM) | 6 Months | 0.96 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Brief Addiction Monitor (BAM) | Posttreatment | 0.86 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Brief Addiction Monitor (BAM) | 3 Months | 0.94 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Brief Addiction Monitor (BAM) | 6 Months | 0.80 score on a scale |
Posttraumatic Diagnostic Scale (PDS-5)
The PDS-5 is a 24-item self-report measure that assesses PTSD symptom severity in the last month according to DSM-5 criteria. The outcome is the change of PDS-5 total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for PDS-5 score 0-80. Higher PDS-5 Score indicates more severe PTSD Symptoms.
Time frame: immediate post-treatment, 3 and 6 months
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| Behavioral: Prolonged Exposure (PE) | Posttraumatic Diagnostic Scale (PDS-5) | Posttreatment | 33.5 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Posttraumatic Diagnostic Scale (PDS-5) | 3 Months | 34.5 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Posttraumatic Diagnostic Scale (PDS-5) | 6 Months | 33.6 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Posttraumatic Diagnostic Scale (PDS-5) | Posttreatment | 36.7 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Posttraumatic Diagnostic Scale (PDS-5) | 3 Months | 37.5 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Posttraumatic Diagnostic Scale (PDS-5) | 6 Months | 36.7 score on a scale |
Short Inventory of Problems - Revised (SIP-R)
The SIP-R assesses alcohol-related consequences. The outcome is the change of SIP-R total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for SIP-R 0-51. Higher score indicates more severe adverse consequences of substance use.
Time frame: immediate post-treatment, 3 and 6 months
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| Behavioral: Prolonged Exposure (PE) | Short Inventory of Problems - Revised (SIP-R) | Posttreatment | 2.61 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Short Inventory of Problems - Revised (SIP-R) | 3 Months | 2.42 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Short Inventory of Problems - Revised (SIP-R) | 6 Months | 3.09 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Short Inventory of Problems - Revised (SIP-R) | Posttreatment | 2.49 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Short Inventory of Problems - Revised (SIP-R) | 3 Months | 2.29 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Short Inventory of Problems - Revised (SIP-R) | 6 Months | 1.72 score on a scale |
Spielberger State Anger Inventory (STAXI)
The STAXI is a commonly used measure of trait and state anxiety. The outcome is the change of STAI total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for STAXI 44-176. Higher score indicates greater intensity of anger.
Time frame: immediate post-treatment, 3 and 6 months
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| Behavioral: Prolonged Exposure (PE) | Spielberger State Anger Inventory (STAXI) | Posttreatment | 93.4 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Spielberger State Anger Inventory (STAXI) | 3 Months | 93.2 score on a scale |
| Behavioral: Prolonged Exposure (PE) | Spielberger State Anger Inventory (STAXI) | 6 Months | 93.2 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Spielberger State Anger Inventory (STAXI) | Posttreatment | 94.6 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Spielberger State Anger Inventory (STAXI) | 3 Months | 94.7 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | Spielberger State Anger Inventory (STAXI) | 6 Months | 94.5 score on a scale |
World Health Organization Disability Assessment Schedule (WHO-DAS-II)
The WHO-DAS-II is an assessment instrument for health and disability. The outcome is the change of WHO-DAS-II total score from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for WHODAS-II 12-60. Higher score indicates more difficulty and disability due to health condition.
Time frame: immediate post-treatment, 3 and 6 months
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| Behavioral: Prolonged Exposure (PE) | World Health Organization Disability Assessment Schedule (WHO-DAS-II) | Posttreatment | 28.6 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Disability Assessment Schedule (WHO-DAS-II) | 3 Months | 28.0 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Disability Assessment Schedule (WHO-DAS-II) | 6 Months | 28.5 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Disability Assessment Schedule (WHO-DAS-II) | Posttreatment | 28.6 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Disability Assessment Schedule (WHO-DAS-II) | 3 Months | 28.7 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Disability Assessment Schedule (WHO-DAS-II) | 6 Months | 28.5 score on a scale |
World Health Organization Quality of Life (WHOQoL-BREF)
The WHOQoL-BREF is a quality of life assessment. The outcome is the change of WHOQoL-BREF assessment sub-category (Physical Health, Psychological, Social Relationships, Environment) scores from baseline (pre-treatment) to the average in the six months post-treatment (measured at immediate post-treatment, 3 and 6 months follow-up visits). Possible range for WHOQOL-BREF 0-100, Physical Health 0-100, Psychological 0-100, Social Relationships 0-100, and Environment 0-100. Higher score indicates better satisfaction with life.
Time frame: immediate post-treatment, 3 and 6 months
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Physical Health - Posttreatment | 47.0 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Physical Health - 3 Months | 47.0 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Physical Health - 6 Months | 47.1 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Psychological - Posttreatment | 49.0 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Psychological - 3 Months | 49.1 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Psychological - 6 Months | 49.5 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Social Relationship - Posttreatment | 45.4 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Social Relationship - 3 Months | 46.2 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Social Relationship - 6 Months | 46.2 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Environment - Posttreatment | 61.1 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Environment - 3 Months | 61.5 score on a scale |
| Behavioral: Prolonged Exposure (PE) | World Health Organization Quality of Life (WHOQoL-BREF) | Environment - 6 Months | 62.3 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Environment - 3 Months | 59.8 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Physical Health - Posttreatment | 48.6 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Social Relationship - Posttreatment | 43.9 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Physical Health - 3 Months | 47.0 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Environment - Posttreatment | 59.5 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Physical Health - 6 Months | 46.9 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Social Relationship - 3 Months | 44.1 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Psychological - Posttreatment | 48.9 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Environment - 6 Months | 60.9 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Psychological - 3 Months | 48.1 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Social Relationship - 6 Months | 45.5 score on a scale |
| Behavioral: Cognitive Processing Therapy (CPT) | World Health Organization Quality of Life (WHOQoL-BREF) | Psychological - 6 Months | 49.1 score on a scale |