Telemedicine Outreach for Post Traumatic Stress in CBOCs (TOP)
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ClinicalTrials.gov Identifier: NCT00821678 |
Recruitment Status :
Completed
First Posted : January 13, 2009
Results First Posted : April 23, 2015
Last Update Posted : January 8, 2019
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Posttraumatic Stress Disorder | Other: Telemedicine Outreach for PTSD | Phase 4 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 265 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Single (Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | Telemedicine Outreach for Post Traumatic Stress in CBOCs |
Study Start Date : | November 2009 |
Actual Primary Completion Date : | September 2012 |
Actual Study Completion Date : | September 2013 |
Arm | Intervention/treatment |
---|---|
Experimental: Arm 1 Telemedicine Outreach for PTSD
Telemedicine-Based Collaborative Care
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Other: Telemedicine Outreach for PTSD
The intervention involves an off-site PTSD care team (tele-psychiatrist, tele-psychologist, tele-pharmacist, and tele-nurse care manager) and uses telemedicine technologies (telephone, interactive video and electronically shared medical records). A dedicated nurse telephone care manager educates/activates patients, identifies preferences, overcomes treatment barriers, monitors symptoms, side-effects and adherence, identifies psychiatric comorbidities, and encourages patient self-management. Tele-pharmacists provide medication management by phone. Tele-psychologists provide Cognitive Processing Therapy via interactive video. Tele-psychiatrists supervise the off-site care team as well as conduct consultations and provide medication management via interactive video.
Other Name: Telemedicine-Based Collaborative Care |
No Intervention: Arm 2 Treatment as usual
Usual Care
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- Change in PTSD Symptom Severity (PDS) [ Time Frame: Baseline, 6 months ]range - 0-51 (higher score represents greater severity)
- Change in Continuous Measure of Depression Symptom Severity (SCL-20) [ Time Frame: Baseline, 6 months ]range - 0-4 (higher score represents greater severity
- Change in Continuous Measure of Alcohol Use (Audit Score) [ Time Frame: Baseline, 6 months ]range - 0-12 (higher score represents greater severity)
- Change in Continuous Measure of Health Status (SF12V PCS) [ Time Frame: 6 months ]range - 0-100 (higher score represents greater physical health status)
- Change in Continuous Measure of Quality of Life (QWB) [ Time Frame: Baseline, 6 months ]range - 0-1 (higher score represents greater wellbeing)
- Satisfaction With Care (ECHO) [ Time Frame: 6 months ]Using any number from 0 to 10, where 0 is the worst care possible and 10 is the best care possible, what number would you use to rate all the care you received for personal or emotional problems in the last 6 months?
- Medication Adherence, Defined as Taking Medication <80% of Days [ Time Frame: 6 months ]0 - taking medication <80% of days; 1 - taking medications >=80%
- Received at Least 8 Sessions of Exposure Based Therapy [ Time Frame: 12 months ]0 - received <8 sessions of exposure based therapy; 1 - received >=8 sessions of exposure based therapy

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- diagnostic Criteria for PTSD (CAPS),
- veterans,
- treated in CBOC
Exclusion Criteria:
- schizophrenia,
- bipolar disorder,
- current substance dependence,
- current specialty PTSD treatment at VA Medical Center,
- no access to telephone,
- hearing or speech impediment,
- terminal illness,
- non-capacity to consent

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00821678
United States, Arkansas | |
Central Arkansas Veterans Healthcare System (North Little Rock) | |
North Little Rock, Arkansas, United States, 72114-1706 | |
United States, California | |
VA Medical Center, Loma Linda | |
Loma Linda, California, United States, 92357 | |
United States, Louisiana | |
Overton Brooks VA Medical Center, Shreveport, LA | |
Shreveport, Louisiana, United States, 71101 |
Principal Investigator: | John C. Fortney, PhD | Central Arkansas Veterans Healthcare System Eugene J. Towbin Healthcare Center, Little Rock, AR |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | VA Office of Research and Development |
ClinicalTrials.gov Identifier: | NCT00821678 |
Other Study ID Numbers: |
MHI 08-098 |
First Posted: | January 13, 2009 Key Record Dates |
Results First Posted: | April 23, 2015 |
Last Update Posted: | January 8, 2019 |
Last Verified: | December 2018 |
telemedicine rural veterans care management psychotherapy |
Stress Disorders, Post-Traumatic Stress Disorders, Traumatic Trauma and Stressor Related Disorders Mental Disorders |