Trial Search Results

Sequenced Treatment Effectiveness for Posttraumatic Stress

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 1,400 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, 3 and 6 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.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

University of Washington

Collaborator: Stanford University

Stanford Investigator(s):

Intervention(s):

  • Drug: Selective serotonin reuptake inhibitor
  • Drug: Serotonin-norepinephrine reuptake inhibitor
  • Behavioral: Written Exposure Therapy

Phase:

Phase 4

Eligibility


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

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Not Recruiting