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Comparative Effectiveness Research in Veterans With PTSD

CSP #591 - CERV-PTSD: Comparative Effectiveness Research in Veterans With PTSD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01928732
Acronym
CERV-PTSD
Enrollment
916
Registered
2013-08-27
Start date
2014-10-31
Completion date
2019-04-18
Last updated
2022-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-Traumatic Stress Disorder

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

VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frameDescription
Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS)immediate post-treatment, 3 and 6 monthsThe 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

MeasureTime frameDescription
Beck Depression Inventory-II (BDI-II)immediate post-treatment, 3 and 6 monthsBDI-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 monthsThe 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 monthsThe 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 monthsThe 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 monthsThe 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 monthsThe 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 monthsThe 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

ArmCount
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
Total916

Baseline characteristics

CharacteristicBehavioral: Cognitive Processing Therapy (CPT)TotalBehavioral: Prolonged Exposure (PE)
Age, Continuous44.9 years45.2 years45.5 years
Any current comorbid psychiatric disorder
Anxiety disorder
166 Participants305 Participants139 Participants
Any current comorbid psychiatric disorder
Mood disorder
332 Participants641 Participants309 Participants
Any current comorbid psychiatric disorder
Obsessive compulsive disorder
29 Participants48 Participants19 Participants
Any current comorbid psychiatric disorder
Substance use disorders
40 Participants72 Participants32 Participants
Any current comorbid psychiatric disorder371 Participants714 Participants343 Participants
Any lifetime comorbid psychiatric disorder
Anxiety disorder
181 Participants330 Participants149 Participants
Any lifetime comorbid psychiatric disorder
Mood disorder
400 Participants798 Participants398 Participants
Any lifetime comorbid psychiatric disorder
Obsessive compulsive disorder
36 Participants60 Participants24 Participants
Any lifetime comorbid psychiatric disorder
Substance use disorders
112 Participants242 Participants130 Participants
Any lifetime comorbid psychiatric disorder424 Participants841 Participants417 Participants
Beck Depression Inventory-II30.0 score on a scale30.2 score on a scale30.3 score on a scale
Beck Depression Inventory-II Suicidality (BDI-II Item 9)156 Participants319 Participants163 Participants
Brief Addiction Monitor0.8 score on a scale0.8 score on a scale0.8 score on a scale
Clinician Administered PTSD Scale-540.3 score on a scale40.1 score on a scale39.9 score on a scale
Ethnicity: Spanish, Hispanic or Latino72 Participants139 Participants67 Participants
Lifetime trauma exposure
Any sexual trauma
163 Participants329 Participants166 Participants
Lifetime trauma exposure
Combat exposure
347 Participants704 Participants357 Participants
Lifetime trauma exposure
Disaster exposure
385 Participants776 Participants391 Participants
Lifetime trauma exposure
Life-threatening illness or injury
163 Participants317 Participants154 Participants
Lifetime trauma exposure
Other traumatic event
354 Participants725 Participants371 Participants
Lifetime trauma exposure
Physical assault
408 Participants794 Participants386 Participants
Lifetime trauma exposure
Serious accident
389 Participants774 Participants385 Participants
Lifetime trauma exposure: Number of event types (of 17)7.4 number of event types7.54 number of event types7.7 number of event types
Married/cohabitating237 Participants483 Participants246 Participants
Number of patients preferring PE treatment at baseline214 Participants446 Participants232 Participants
Positive VA Military Sexual Trauma Screen133 Participants267 Participants134 Participants
Positive VA Traumatic Brain Injury Screen281 Participants575 Participants294 Participants
Post-high school education192 Participants408 Participants216 Participants
Posttraumatic Diagnostic Scale50.5 score on a scale50.63 score on a scale50.7 score on a scale
PTSD disability
Approved
202 Participants388 Participants186 Participants
PTSD disability
Denied
19 Participants45 Participants26 Participants
PTSD disability
Never applied
109 Participants234 Participants125 Participants
PTSD disability
Pending
129 Participants245 Participants116 Participants
Race/Ethnicity, Customized
American Indian/Alaskan Native
15 Participants33 Participants18 Participants
Race/Ethnicity, Customized
Asian
11 Participants25 Participants14 Participants
Race/Ethnicity, Customized
Black
130 Participants249 Participants119 Participants
Race/Ethnicity, Customized
Native Hawaiian/Pacific Islander
10 Participants17 Participants7 Participants
Race/Ethnicity, Customized
Other
25 Participants46 Participants21 Participants
Race/Ethnicity, Customized
White
289 Participants590 Participants301 Participants
Receiving psychotherapy98 Participants193 Participants95 Participants
Service Era
Gulf War
87 Participants172 Participants85 Participants
Service Era
OEF/OIF/OND
270 Participants530 Participants260 Participants
Service Era
Other
59 Participants125 Participants66 Participants
Service Era
Vietnam
77 Participants159 Participants82 Participants
Sex: Female, Male
Female
92 Participants186 Participants94 Participants
Sex: Female, Male
Male
369 Participants730 Participants361 Participants
Short Inventory of Problems-Revised3.3 score on a scale3.4 score on a scale3.5 score on a scale
Spielberger Trait Anger Expression Inventory
Anger Expression
36.4 score on a scale36.9 score on a scale37.3 score on a scale
Spielberger Trait Anger Expression Inventory
State Anger
17.9 score on a scale17.9 score on a scale17.8 score on a scale
Spielberger Trait Anger Expression Inventory
Trait Anger
24.2 score on a scale24.2 score on a scale24.1 score on a scale
Taking psychotropic medication317 Participants620 Participants303 Participants
Unemployed263 Participants534 Participants271 Participants
World Health Organization Disability Adjustment Scale-II29.7 score on a scale29.6 score on a scale29.4 score on a scale
World Health Organization Quality of Life-BREF
Environment
57.4 score on a scale57.8 score on a scale58.2 score on a scale
World Health Organization Quality of Life-BREF
Physical Health
43.7 score on a scale44.1 score on a scale44.4 score on a scale
World Health Organization Quality of Life-BREF
Psychological
46.4 score on a scale46.5 score on a scale46.5 score on a scale
World Health Organization Quality of Life-BREF
Social Relationships
40.6 score on a scale41.0 score on a scale41.3 score on a scale

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
1 / 4552 / 461
other
Total, other adverse events
42 / 45565 / 461
serious
Total, serious adverse events
55 / 45563 / 461

Outcome results

Primary

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

ArmMeasureGroupValue (MEAN)
Behavioral: Prolonged Exposure (PE)Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS)Posttreatment24.3 score on a scale
Behavioral: Prolonged Exposure (PE)Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS)3 Months26.4 score on a scale
Behavioral: Prolonged Exposure (PE)Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS)6 Months24.8 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS)Posttreatment27.2 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS)3 Months28.7 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Change in PTSD Symptom Severity on the Clinician-Administered PTSD Scale (CAPS)6 Months26.9 score on a scale
Comparison: Overall Treatment Effect Response Odds Ratio (OR). Response is defined as greater than or equal to 10 point improvement in severity.95% CI: [1, 1.65]
Comparison: Overall Treatment Effect Loss of Diagnosis Odds Ratio (OR). Loss of Diagnosis is defined as Response, plus no longer meeting DSM-5 symptom criteria and severity less than 25.95% CI: [1.12, 1.74]
Comparison: Overall Treatment Effect Remission Odds Ratio (OR). Remission is defined as loss of diagnosis plus severity less than 12.95% CI: [1.24, 2]
Secondary

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

ArmMeasureGroupValue (MEAN)
Behavioral: Prolonged Exposure (PE)Beck Depression Inventory-II (BDI-II)Posttreatment22.0 score on a scale
Behavioral: Prolonged Exposure (PE)Beck Depression Inventory-II (BDI-II)3 Months22.2 score on a scale
Behavioral: Prolonged Exposure (PE)Beck Depression Inventory-II (BDI-II)6 Months21.9 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Beck Depression Inventory-II (BDI-II)Posttreatment22.7 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Beck Depression Inventory-II (BDI-II)3 Months23.6 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Beck Depression Inventory-II (BDI-II)6 Months22.9 score on a scale
Secondary

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

ArmMeasureGroupValue (MEAN)
Behavioral: Prolonged Exposure (PE)Brief Addiction Monitor (BAM)Posttreatment0.88 score on a scale
Behavioral: Prolonged Exposure (PE)Brief Addiction Monitor (BAM)3 Months1.0 score on a scale
Behavioral: Prolonged Exposure (PE)Brief Addiction Monitor (BAM)6 Months0.96 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Brief Addiction Monitor (BAM)Posttreatment0.86 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Brief Addiction Monitor (BAM)3 Months0.94 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Brief Addiction Monitor (BAM)6 Months0.80 score on a scale
Secondary

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

ArmMeasureGroupValue (MEAN)
Behavioral: Prolonged Exposure (PE)Posttraumatic Diagnostic Scale (PDS-5)Posttreatment33.5 score on a scale
Behavioral: Prolonged Exposure (PE)Posttraumatic Diagnostic Scale (PDS-5)3 Months34.5 score on a scale
Behavioral: Prolonged Exposure (PE)Posttraumatic Diagnostic Scale (PDS-5)6 Months33.6 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Posttraumatic Diagnostic Scale (PDS-5)Posttreatment36.7 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Posttraumatic Diagnostic Scale (PDS-5)3 Months37.5 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Posttraumatic Diagnostic Scale (PDS-5)6 Months36.7 score on a scale
Secondary

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

ArmMeasureGroupValue (MEAN)
Behavioral: Prolonged Exposure (PE)Short Inventory of Problems - Revised (SIP-R)Posttreatment2.61 score on a scale
Behavioral: Prolonged Exposure (PE)Short Inventory of Problems - Revised (SIP-R)3 Months2.42 score on a scale
Behavioral: Prolonged Exposure (PE)Short Inventory of Problems - Revised (SIP-R)6 Months3.09 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Short Inventory of Problems - Revised (SIP-R)Posttreatment2.49 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Short Inventory of Problems - Revised (SIP-R)3 Months2.29 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Short Inventory of Problems - Revised (SIP-R)6 Months1.72 score on a scale
Secondary

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

ArmMeasureGroupValue (MEAN)
Behavioral: Prolonged Exposure (PE)Spielberger State Anger Inventory (STAXI)Posttreatment93.4 score on a scale
Behavioral: Prolonged Exposure (PE)Spielberger State Anger Inventory (STAXI)3 Months93.2 score on a scale
Behavioral: Prolonged Exposure (PE)Spielberger State Anger Inventory (STAXI)6 Months93.2 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Spielberger State Anger Inventory (STAXI)Posttreatment94.6 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Spielberger State Anger Inventory (STAXI)3 Months94.7 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)Spielberger State Anger Inventory (STAXI)6 Months94.5 score on a scale
Secondary

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

ArmMeasureGroupValue (MEAN)
Behavioral: Prolonged Exposure (PE)World Health Organization Disability Assessment Schedule (WHO-DAS-II)Posttreatment28.6 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Disability Assessment Schedule (WHO-DAS-II)3 Months28.0 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Disability Assessment Schedule (WHO-DAS-II)6 Months28.5 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Disability Assessment Schedule (WHO-DAS-II)Posttreatment28.6 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Disability Assessment Schedule (WHO-DAS-II)3 Months28.7 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Disability Assessment Schedule (WHO-DAS-II)6 Months28.5 score on a scale
Secondary

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

ArmMeasureGroupValue (MEAN)
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Physical Health - Posttreatment47.0 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Physical Health - 3 Months47.0 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Physical Health - 6 Months47.1 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Psychological - Posttreatment49.0 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Psychological - 3 Months49.1 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Psychological - 6 Months49.5 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Social Relationship - Posttreatment45.4 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Social Relationship - 3 Months46.2 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Social Relationship - 6 Months46.2 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Environment - Posttreatment61.1 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Environment - 3 Months61.5 score on a scale
Behavioral: Prolonged Exposure (PE)World Health Organization Quality of Life (WHOQoL-BREF)Environment - 6 Months62.3 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Environment - 3 Months59.8 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Physical Health - Posttreatment48.6 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Social Relationship - Posttreatment43.9 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Physical Health - 3 Months47.0 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Environment - Posttreatment59.5 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Physical Health - 6 Months46.9 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Social Relationship - 3 Months44.1 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Psychological - Posttreatment48.9 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Environment - 6 Months60.9 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Psychological - 3 Months48.1 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Social Relationship - 6 Months45.5 score on a scale
Behavioral: Cognitive Processing Therapy (CPT)World Health Organization Quality of Life (WHOQoL-BREF)Psychological - 6 Months49.1 score on a scale

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026