DElivery of Self Training and Education for Stressful Situations-Primary Care Version

The study is a multi-site trial evaluating the efficacy of DESTRESS-PC (DElivery of Self-TRaining and Education for Stressful Situations, primary care version), a brief, web-based self-management intervention for PTSD designed for delivery in primary care. Participants randomized to DESTRESS-PC log on to a secure website for self-CBT 3 times per week for 6 weeks and receive RN nurse care manager ("DESTRESS Nurse") contact every two weeks. DESTRESS Nurses introduce the approach, monitor, answer questions, and insure primary care provider collaboration. The control intervention is optimized usual primary care. Blinded raters assess PTSD symptoms, depression, anxiety, somatic symptoms, physical health status, and occupational functioning at four timepoints. All study participants receive RN care management and are under the care of a primary care provider trained in evidence-based PTSD treatment who receives status reports from the DESTRESS nurse to include baseline psychiatric status.

Inclusion criteria

• Referred by a primary care providers in a participating primary care clinic.
• Deployed to either Operation Iraqi Freedom or Enduring Freedom.
• War-related trauma while deployed (may include military sexual trauma).
• Current PTSD as addressed by the CAPS interview.
• Reports routine access to computer, internet, and email.
• Successfully uses Internet to coordinate baseline assessment appointment.
• Provides research informed consent using local IRB-approved form.
• Plans continued care at the enrolling primary care clinic for at least 4 months.

Exclusion criteria

• Actively engaged in specialty mental health care in the previous two months.
• Failed specialty mental health treatment for PTSD or associated condition.
• Acute psychosis, psychotic episode, or psychotic disorder diagnosis within the past two years.
• Active substance dependence disorder in the past year.
• Active suicidal or violent ideation within the past two months.
• Currently on an antipsychotic or mood-stabilizing agent.
• Unstable administration schedule or dosing of any antidepressant, anxiolytic, or sedative-hypnotic (i.e., will exclude for any related medication changes in the two-months prior to randomization).
• Acute or unstable physical illness.