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Sequenced Treatment Effectiveness for Posttraumatic Stress

Comparative Effectiveness PTSD Trial of Sequenced Pharmacotherapy and Psychotherapy in Primary Care

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04597190
Acronym
STEPS
Enrollment
700
Registered
2020-10-22
Start date
2020-06-01
Completion date
2024-08-01
Last updated
2025-05-08

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

Conditions

PTSD

Keywords

antidepressants, exposure therapy, primary care

Brief summary

Individuals with PTSD are more likely to engage in unhealthy behaviors such as tobacco use, drug use, alcohol misuse, and have high rates of morbidity/mortality. PTSD negatively impacts marriages, educational attainment, and occupational functioning. Some patients with PTSD can be successfully referred to specialty mental health clinics, but most patients with PTSD cannot engage in specialty care because of geographical, financial and cultural barriers and must be treated in primary care. However, policy makers do not know the best way to treat PTSD in primary care clinics, especially for patients who do not respond to the initial treatment choice. There are effective treatments for PTSD that are feasible to deliver in primary care. These treatments include commonly prescribed antidepressants and brief exposure-based therapies. However, because there are no head-to-head comparisons between pharmacotherapy and psychotherapy in primary care settings, primary care providers do not know which treatments to recommend to their patients. In addition, despite high treatment non-response rates, very few studies have examined which treatment should be recommend next when patients do not respond well to the first, and no such studies have been conducted in primary care settings. This trial will be conducted in Federally Qualified Health Centers and VA Medical Centers, where the prevalence of both past trauma exposure and PTSD are particularly high. The investigators will enroll 700 primary care patients. The investigators propose to 1) compare outcomes among patients randomized to initially receive pharmacotherapy or brief psychotherapy, 2) compare outcomes among patients randomized to treatment sequences (i.e., switching and augmenting) for patients not responding to the initial treatment and 3) examine variation in treatment outcomes among different subgroups of patients. Telephone and web surveys will be used to assessed outcomes important to patients, like self-reported symptom burden, side-effects, health related quality of life, and recovery outcomes, at baseline, 4 and 8 months. Results will help patients and primary care providers choose which treatment to try first and which treatment to try second if the first is not effective.

Detailed description

Background: In primary care settings, PTSD frequently goes undetected and untreated. When PTSD is diagnosed in primary care, treatment is usually inadequate and outcomes are poor. This is highly problematic because many patients with PTSD prefer receiving care in primary care settings, and less than half are successfully referred to the specialty mental health setting. This is especially a concern for safety net primary settings such as Federally Qualified Health Centers and VA Medical Centers, where the prevalence of both past trauma exposure and PTSD are particularly high. However, there are effective pharmacotherapy and psychotherapy treatments for PTSD that are feasible to deliver in primary care. Objective: Because there are no head-to-head comparisons of pharmacotherapy and psychotherapy for PTSD among primary care patients, the investigators propose to 1) compare outcomes among patients randomized to initially receive pharmacotherapy or brief psychotherapy, 2) compare outcomes among patients randomized to treatment sequences (i.e., switching and augmenting) for patients not responding to the initial treatment and 3) examine variation in treatment outcomes among different subgroups of patients. Methods: This multi-site trial will enroll 700 patients meeting clinical criteria for PTSD from 7 Federally Qualified Health Centers and 8 VA Medical Centers. The pharmacotherapy treatments are sertraline, fluoxetine, paroxetine and venlafaxine. The psychotherapy treatment is Written Exposure Therapy. Telephone and web surveys will be used to assessed outcomes (patient treatment engagement, self-reported symptom burden, health related quality of life, and recovery outcomes) at baseline, 4 and 8 months. Patients will be the unit of the intent-to-treat analysis. Multiple imputation will be used for missing data. Mixed-models will be used to test hypotheses. Significance: Due to a lack of head-to-head comparisons between pharmacotherapy and psychotherapy protocols, clinical practice guidelines for PTSD provide contradictory recommendations about pharmacotherapy and psychotherapy. In particular, PTSD clinical practice guidelines have little to offer primary care providers because so few trials have been conducted in this setting. The proposed large pragmatic trial will compare, head-to-head, FDA approved PTSD medications with a brief trauma-focused psychotherapy that is evidence-based and feasible to deliver in primary care. In addition, despite high treatment non-response rates, very few trials have examined treatment sequencing and none have done so in the primary care setting. For patients not responding to the initial treatment, the proposed research is powered to compare, head-to-head, alternative treatment sequences that are feasible to deliver in primary care.

Interventions

Prescribers and patients choose among three selective serotonin reuptake inhibitors (SSRI), sertraline, paroxetine, or fluoxetine based on patient's treatment history (i.e., failed SSRI trials due to side-effects or lack of efficacy) and preference. If a patient experiences problematic side effects after taking their choice of SSRI, the provider may switch them to another of the SSRI options during the first 8 weeks of follow-up. Patients on any antidepressant (including SSRIs) at enrollment will be cross-tapered over four weeks to either fluoxetine, sertraline or paroxetine (i.e., the old drug will be tapered down while the new drug is tapering up).

DRUGSerotonin-norepinephrine reuptake inhibitor

Prescribers will prescribe venlafaxine.

BEHAVIORALWritten Exposure Therapy

Written Exposure Therapy will be delivered during six 30 minute sessions. The first session includes psychoeducation about symptoms of PTSD, provides a treatment rationale for approaching the trauma memory, and discusses the use of writing as a means of doing so. In sessions 2-6, patients will write about the memory of their worst traumatic event for 20 minutes, with a focus on details of the event and thoughts and feelings that occurred during the event. Patients are directed to write about the same trauma memory during each session. The session ends with the therapist instructing the patient to allow themselves to experience any trauma-related memories, images, thoughts, and feelings in the interval between sessions. The therapist reads the narrative between sessions to make sure instructions were followed. Feedback about the narrative is provided to the patient at the beginning of sessions 3-6. This feedback is used to prompt the patient for writing in the current session.

Sponsors

Stanford University
CollaboratorOTHER
Boston University
CollaboratorOTHER
Washington State University
CollaboratorOTHER
Patient-Centered Outcomes Research Institute
CollaboratorOTHER
University of Washington
Lead SponsorOTHER

Study design

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

Masking description

The survey team members will be masked to which arm the study participant has been randomized. The PI, Co-PIs, and Co-Is will not have access to the outcomes until the primary data collection phase has been completed. The statistician will present outcomes by arm to the Data Safety Monitoring Board (DSMB) members during closed sessions of DSMB meetings.

Intervention model description

Patients will be randomized to treatment sequences, stratified by site and baseline antidepressant use.

Eligibility

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

Inclusion criteria

* Screen positive for PTSD (PC-PTSD\>=3 AND PCL\>=33) * Screen positive for trauma (Brief Trauma questionnaire)

Exclusion criteria

* Diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder or dementia * Current prescription of venlafaxine * Change in any psychotropic prescription in the past 2 months * A scheduled specialty mental health appointment or preference for specialty mental health care * Pregnant * Terminally ill * Prisoner * Unable to communicate in English or Spanish * \<18 years of age * Impaired decision making capacity

Design outcomes

Primary

MeasureTime frameDescription
PTSD Symptoms4 months (Hypothesis 1)Self reported burden of PTSD symptoms (PCL-5) (range 0-80, higher scores are worse)

Secondary

MeasureTime frameDescription
Mental Health Related Quality of Life: SF-12V, Mental Health Component Summary Score4 months (Hypothesis 1)SF-12V, Mental Health Component Summary Score (range 0-100, higher scores are better)
Depression Symptoms4 months (Hypothesis 1)Self reported burden of depression symptoms (PHQ-9) (range 0-27, higher scores are worse)
Generalized Anxiety Symptoms4 months (Hypothesis 1)Self reported burden of anxiety symptoms (GAD-7) (range 0-21, higher scores are worse)

Other

MeasureTime frameDescription
Number of Severe and Moderate Side Effects4 months (Hypothesis 1)Self reported severity of specific side-effects

Countries

United States

Participant flow

Participants by arm

ArmCount
SSRI Then Augmentation by WET
Prescribers will prescribe one of three SSRIs (sertraline, fluoxetine or paroxetine). Patients who do not respond to treatment by four months will have their treatment augmented by Written Exposure Therapy (WET) delivered by an integrated behavioral health consultant. Selective serotonin reuptake inhibitor: Prescribers and patients choose among three selective serotonin reuptake inhibitors (SSRI), sertraline, paroxetine, or fluoxetine. If a patient experiences problematic side effects after taking their choice of SSRI, the provider may switch them to another of the SSRI options during the first 8 weeks of follow-up. Patients on any antidepressant (including SSRIs) at enrollment will be cross-tapered over four weeks to either fluoxetine, sertraline or paroxetine. Written Exposure Therapy: Written Exposure Therapy will be delivered during six 30 minute sessions. The first session includes psychoeducation. In sessions 2-6, patients will write about the memory of their worst traumatic event for 20 minutes, with a focus on details of the event and thoughts and feelings that occurred during the event. Patients are directed to write about the same trauma memory during each session. The therapist reads the narrative between sessions to make sure instructions were followed. Feedback about the narrative is provided to the patient at the beginning of sessions 3-6. This feedback is used to prompt the patient for writing in the current session.
169
SSRI Then Switch to SNRI
Prescribers will prescribe one of three SSRIs (sertraline, fluoxetine or paroxetine). Patients who do not respond to treatment by four months will have their treatment switched to the SNRI (serotonin-norepinephrine reuptake Inhibitor) venlafaxine. Selective serotonin reuptake inhibitor: Prescribers and patients choose among three selective serotonin reuptake inhibitors (SSRI), sertraline, paroxetine, or fluoxetine based on patient's treatment history (i.e., failed SSRI trials due to side-effects or lack of efficacy) and preference. If a patient experiences problematic side effects after taking their choice of SSRI, the provider may switch them to another of the SSRI options during the first 8 weeks of follow-up. Patients on any antidepressant (including SSRIs) at enrollment will be cross-tapered over four weeks to either fluoxetine, sertraline or paroxetine (i.e., the old drug will be tapered down while the new drug is tapering up). Serotonin-norepinephrine reuptake inhibitor: Prescribers will prescribe venlafaxine.
179
WET Then Switch to SSRI
Integrated behavioral health consultants will deliver WET. Patients who do not respond to treatment by four months will be switched to one of three SSRIs (sertraline, fluoxetine or paroxetine). Written Exposure Therapy: Written Exposure Therapy will be delivered during six 30 minute sessions. The first session includes psychoeducation. In sessions 2-6, patients will write about the memory of their worst traumatic event for 20 minutes, with a focus on details of the event and thoughts and feelings that occurred during the event. Patients are directed to write about the same trauma memory during each session. The therapist reads the narrative between sessions to make sure instructions were followed. Feedback about the narrative is provided to the patient at the beginning of sessions 3-6. This feedback is used to prompt the patient for writing in the current session. Selective serotonin reuptake inhibitor: Prescribers and patients choose among three selective serotonin reuptake inhibitors (SSRI), sertraline, paroxetine, or fluoxetine. If a patient experiences problematic side effects after taking their choice of SSRI, the provider may switch them to another of the SSRI options during the first 8 weeks of follow-up. Patients on any antidepressant (including SSRIs) at enrollment will be cross-tapered over four weeks to either fluoxetine, sertraline or paroxetine.
352
Total700

Baseline characteristics

CharacteristicSSRI Then Augmentation by WETSSRI Then Switch to SNRIWET Then Switch to SSRITotal
Age, Continuous46.6 Years
STANDARD_DEVIATION 15.1
44.4 Years
STANDARD_DEVIATION 15.6
44.8 Years
STANDARD_DEVIATION 15.4
45.1 Years
STANDARD_DEVIATION 15.4
Ethnicity (NIH/OMB)
Hispanic or Latino
21 Participants28 Participants51 Participants100 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
110 Participants105 Participants222 Participants437 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
38 Participants46 Participants79 Participants163 Participants
PTSD Check List (PCL-5)53.2 units on a scale (range 0-80)
STANDARD_DEVIATION 11.5
52.8 units on a scale (range 0-80)
STANDARD_DEVIATION 10.9
52.6 units on a scale (range 0-80)
STANDARD_DEVIATION 11
52.8 units on a scale (range 0-80)
STANDARD_DEVIATION 11.1
Race/Ethnicity, Customized
American Indian, Alaskan Native, or other Indigenous group
0 Participants5 Participants3 Participants8 Participants
Race/Ethnicity, Customized
Another Identity
4 Participants8 Participants11 Participants23 Participants
Race/Ethnicity, Customized
Arab or Middle Eastern
3 Participants1 Participants0 Participants4 Participants
Race/Ethnicity, Customized
Asian
2 Participants8 Participants12 Participants22 Participants
Race/Ethnicity, Customized
Black or African American
30 Participants28 Participants70 Participants128 Participants
Race/Ethnicity, Customized
Missing
26 Participants24 Participants42 Participants92 Participants
Race/Ethnicity, Customized
Multi-race
11 Participants10 Participants27 Participants48 Participants
Race/Ethnicity, Customized
Native Hawaiian or Pacific Islander
1 Participants1 Participants4 Participants6 Participants
Race/Ethnicity, Customized
White
92 Participants94 Participants183 Participants369 Participants
Region of Enrollment
United States
169 participants179 participants352 participants700 participants
Sex/Gender, Customized
Another identity
1 Participants1 Participants2 Participants4 Participants
Sex/Gender, Customized
Man
98 Participants93 Participants177 Participants368 Participants
Sex/Gender, Customized
Missing
25 Participants31 Participants51 Participants107 Participants
Sex/Gender, Customized
Non-binary or gender fluid
1 Participants3 Participants3 Participants7 Participants
Sex/Gender, Customized
Transgender Man
0 Participants1 Participants0 Participants1 Participants
Sex/Gender, Customized
Transgender Women
0 Participants1 Participants0 Participants1 Participants
Sex/Gender, Customized
Woman
44 Participants49 Participants119 Participants212 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 1690 / 1791 / 352
other
Total, other adverse events
34 / 16935 / 17960 / 352
serious
Total, serious adverse events
32 / 16934 / 17963 / 352

Outcome results

Primary

PTSD Symptoms

Self reported burden of PTSD symptoms (PCL-5) (range 0-80, higher scores are worse)

Time frame: 4 months (Hypothesis 1)

ArmMeasureValue (MEAN)Dispersion
SSRI Then Augmentation by WETPTSD Symptoms39.3 units on a scaleStandard Deviation 17.8
SSRI Then Switch to SNRIPTSD Symptoms38.6 units on a scaleStandard Deviation 17
WET Then Switch to SSRIPTSD Symptoms40.5 units on a scaleStandard Deviation 18.4
Primary

PTSD Symptoms

Self reported burden of PTSD symptoms (PCL-5) (range 0-80, higher scores are worse)

Time frame: 8 Months (Hypotheses 2a and 2b)

Population: Participants not responding to treatment at 4-months who completed the 8-month survey

ArmMeasureValue (MEAN)Dispersion
SSRI Then Augmentation by WETPTSD Symptoms49.3 units on a scaleStandard Deviation 17
SSRI Then Switch to SNRIPTSD Symptoms42.1 units on a scaleStandard Deviation 17.2
WET Then Switch to SSRIPTSD Symptoms44.5 units on a scaleStandard Deviation 17.3
Secondary

Depression Symptoms

Self reported burden of depression symptoms (PHQ-9) (range 0-27, higher scores are worse)

Time frame: 4 months (Hypothesis 1)

Population: Participants completing the 4-month survey

ArmMeasureValue (MEAN)Dispersion
SSRI Then Augmentation by WETDepression Symptoms12.6 units on a scaleStandard Deviation 6
SSRI Then Switch to SNRIDepression Symptoms12.3 units on a scaleStandard Deviation 5.9
WET Then Switch to SSRIDepression Symptoms13.3 units on a scaleStandard Deviation 6.2
Secondary

Depression Symptoms

Self reported burden of depression symptoms (PHQ-9) (range 0-27, higher scores are worse)

Time frame: 8 Months (Hypotheses 2a and 2b)

Population: Participants not responding to treatment at 4-months who completed the 8-month survey

ArmMeasureValue (MEAN)Dispersion
SSRI Then Augmentation by WETDepression Symptoms14.3 units on a scaleStandard Deviation 6.4
SSRI Then Switch to SNRIDepression Symptoms13.4 units on a scaleStandard Deviation 5.7
WET Then Switch to SSRIDepression Symptoms14.6 units on a scaleStandard Deviation 6.1
Secondary

Generalized Anxiety Symptoms

Self reported burden of anxiety symptoms (GAD-7) (range 0-21, higher scores are worse)

Time frame: 8 Months (Hypotheses 2a and 2b)

Population: Participants not responding to treatment at 4-months who completed the 8-month survey

ArmMeasureValue (MEAN)Dispersion
SSRI Then Augmentation by WETGeneralized Anxiety Symptoms12.5 units on a scaleStandard Deviation 5.5
SSRI Then Switch to SNRIGeneralized Anxiety Symptoms11.8 units on a scaleStandard Deviation 5.7
WET Then Switch to SSRIGeneralized Anxiety Symptoms12.9 units on a scaleStandard Deviation 5.6
Secondary

Generalized Anxiety Symptoms

Self reported burden of anxiety symptoms (GAD-7) (range 0-21, higher scores are worse)

Time frame: 4 months (Hypothesis 1)

Population: Participants completing the survey at 4-months

ArmMeasureValue (MEAN)Dispersion
SSRI Then Augmentation by WETGeneralized Anxiety Symptoms10.7 units on a scaleStandard Deviation 5.5
SSRI Then Switch to SNRIGeneralized Anxiety Symptoms10.4 units on a scaleStandard Deviation 5.2
WET Then Switch to SSRIGeneralized Anxiety Symptoms11.2 units on a scaleStandard Deviation 6
Secondary

Mental Health Related Quality of Life: SF-12V, Mental Health Component Summary Score

SF-12V, Mental Health Component Summary Score (range 0-100, higher scores are better)

Time frame: 4 months (Hypothesis 1)

ArmMeasureValue (MEAN)Dispersion
SSRI Then Augmentation by WETMental Health Related Quality of Life: SF-12V, Mental Health Component Summary Score34.7 units on a scaleStandard Deviation 11.6
SSRI Then Switch to SNRIMental Health Related Quality of Life: SF-12V, Mental Health Component Summary Score34.1 units on a scaleStandard Deviation 12.2
WET Then Switch to SSRIMental Health Related Quality of Life: SF-12V, Mental Health Component Summary Score32.9 units on a scaleStandard Deviation 11
Secondary

Mental Health Related Quality of Life: SF-12V, Mental Health Component Summary Score

SF-12V, Mental Health Component Summary Score (range 0-100, higher scores are better)

Time frame: 8 Months (Hypotheses 2a and 2b)

Population: Participants not responding to treatment at 4-months who completed the 8-month survey

ArmMeasureValue (MEAN)Dispersion
SSRI Then Augmentation by WETMental Health Related Quality of Life: SF-12V, Mental Health Component Summary Score29.4 units on a scaleStandard Deviation 12.3
SSRI Then Switch to SNRIMental Health Related Quality of Life: SF-12V, Mental Health Component Summary Score32.0 units on a scaleStandard Deviation 12.8
WET Then Switch to SSRIMental Health Related Quality of Life: SF-12V, Mental Health Component Summary Score31.7 units on a scaleStandard Deviation 12.2
Other Pre-specified

Number of Severe and Moderate Side Effects

Self reported severity of specific side-effects

Time frame: 4 months (Hypothesis 1)

Population: Participants completing the 4-month survey

ArmMeasureValue (MEAN)Dispersion
SSRI Then Augmentation by WETNumber of Severe and Moderate Side Effects2.9 Number of side-effectsStandard Deviation 2.7
SSRI Then Switch to SNRINumber of Severe and Moderate Side Effects2.6 Number of side-effectsStandard Deviation 2.5
WET Then Switch to SSRINumber of Severe and Moderate Side Effects2.9 Number of side-effectsStandard Deviation 2.4
Other Pre-specified

Number of Severe and Moderate Side Effects

Self reported severity of specific side-effects

Time frame: 8 Months (Hypotheses 2a and 2b)

Population: Participants not responding to treatment at 4-months who completed the 8-month survey

ArmMeasureValue (MEAN)Dispersion
SSRI Then Augmentation by WETNumber of Severe and Moderate Side Effects3.3 Number of side-effectsStandard Deviation 2.2
SSRI Then Switch to SNRINumber of Severe and Moderate Side Effects2.9 Number of side-effectsStandard Deviation 2.6
WET Then Switch to SSRINumber of Severe and Moderate Side Effects3.2 Number of side-effectsStandard Deviation 2.6

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026