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

Online Early Resilience Intervention for Combat-Related PTSD in Military Primary Healthcare Settings: A Randomized Trial of DESTRESS-PC

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01474057
Acronym
DESTRESS-PC
Enrollment
133
Registered
2011-11-17
Start date
2008-05-31
Completion date
2011-07-31
Last updated
2012-01-12

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

Conditions

Posttraumatic Stress Disorder (PTSD)

Keywords

PTSD, combat trauma, telemedicine, primary care interventions, CBT, self-managed treatment, web-based intervention, internet treatment

Brief summary

This study will compare a cognitive-behavioral online self-management intervention designed for primary care treatment of war-related PTSD to a control intervention, optimized usual primary care PTSD treatment. Patients with PTSD will be trained to use the online PTSD treatment website and asked to do so three times per week for six weeks. They will have phone and email access to a nurse trained to assist them in their treatment program. Three scheduled phone check-ins during the six week treatment period will provide ongoing contact with patients during treatment. The investigators will assess PTSD symptoms, depression, anxiety and somatic symptoms, physical health status and occupational functioning on three occasions: before the intervention, at the end of the treatment period, and six weeks after the end of treatment.

Detailed description

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.

Interventions

BEHAVIORALDESTRESS-PC

An online nurse-assisted, self-management intervention designed for primary care treatment of war-related PTSD, this intervention will consist of 3 weekly logins to a secure website for a period of 6 weeks. A DESTRESS Nurse will train the participant to use the website and will monitor their progress and report key information back to the primary care physician.

OTHEROptimized Usual Primary Care PTSD treatment

Participants receive usual Primary Care treatment that is administered by the primary care physician; the DESTRESS Nurse monitors the participants' progress throughout the study.

Sponsors

United States Department of Defense
CollaboratorFED
National Institute of Mental Health (NIMH)
CollaboratorNIH
Henry M. Jackson Foundation for the Advancement of Military Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
PTSD Checklist (PCL)Baseline and 6 weeks, 12 weeks, and 18 weeks post randomizationSymptoms of PTSD were assessed using the PTSD Checklist-Military Version (PCL). The PCL is a self-report measure developed for measuring PTSD symptom severity and for estimating PTSD caseness when administration of a structured clinical interview is not feasible. Respondents rate PCL items on a 5-point scale ('not at all' through extremely') to indicate the degree to which they have been bothered by each of 17 PTSD symptoms during the past month. Possible PCL scores range from 17 to 85.

Secondary

MeasureTime frameDescription
PRIME-MD PHQbaseline and 6 weeks,12 weeks, and 18 weeks post randomizationThe PHQ is a brief self-report assessment of common mental disorders developed specifically for primary care. PHQ allows brief provisional primary care diagnoses of several disorders including major depression, panic disorder, other anxiety disorder, and multi-somatoform disorder. We used the PHQ for baseline and follow-up assessments of depression, anxiety (panic and generalized anxiety), and somatic symptom severity, assessments with excellent correspondence to DSM-IV diagnostic criteria.
Medical Outcomes Study Short Form-36 (SF-36)baseline, 6 wks, 12 wks, and 18wksThe SF-36 is a widely used measure of health related quality of life with established reliability and validity. The SF-36 was used to describe the study sample, compare functional status of the intervention groups at baseline, and assess change in functional over the course of the study.
Attitude Regarding Mental Health Treatmentsbaseline, 6 weeks, 12 weeks, and 18 weeksWe used two questions from Hoge and colleagues (2004): 'I don't trust mental health professionals,' and 'Mental health care doesn't work.' Both questions are rated using a five-point Likert-type scale. We also used two questions that rate attitudes regarding psychotherapy treatment ('Psychotherapy patients are wasting money,' and 'Therapy can help an individual'). The latter two questions, rated on the same 5-point scale, were part of a longer measure used to evaluate stigma in primary care patients with anxiety disorders.
World Health Organization Health and Performance Questionnaire (HPQ).baseline, 6 weeks, 12 weeks, and 18 weeksThe HPQ is an assessment instrument to estimate the costs of workplace health problems using a self-report instrument. Specific areas assessed include job performance, absenteeism, and work related critical incidents.

Countries

United States

Outcome results

None listed

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