Post Traumatic Stress Disorder |
Ptsd |
Clinical Trial: Telephone Care as a Substitute for Routine Psychiatric Medication Management
This study is currently recruiting patients.
|
Purpose
Telemedicine uses communications technologies to provide health care when distance separates participants. Applied to general medical care practice, telemedicine is associated with improved continuity of care, cost-effectiveness, and improved service quality. To date, all evaluations of telepsychiatry have concentrated on video technology. The telephone is a more readily available and less expensive communication technology that has not been evaluated as a method of health services delivery in the medication management of stable psychiatric outpatients.
The objectives of this study are to answer the following questions: 1) Does substituting brief, scheduled, clinician-initiated telephone calls (telephone care) for routine psychiatric medication management visits reduce overall healthcare utilization? and, 2) Is substituting brief, scheduled, clinician-initiated telephone calls (telephone care) for routine psychiatric medication management visits as effective as routine care? We will enroll 346 psychiatrically stable subjects who carry a diagnosis of major depression, post-traumatic stress disorder (PTSD), or non-PTSD anxiety disorder. We are using a balanced randomization strategy to assign subjects to routine care or telephone care for a two-year period within each provider panel. Patients randomized to receive routine care will be scheduled to see their psychiatric medication provider at the recommended interval. Patients randomized to receive telephone care are scheduled to see their provider at twice the recommended clinic visit interval, and two ten-minute telephone contacts are scheduled at a specific time at standard 0.67 and 1.3 times the multiple of the recommended interval.
At two years, we will use ten data sources to compare two primary outcomes (total Veterans Health Administration (VHA) health services utilization and mental health component scores from the SF-12-V) as well as VHA costs, imputed non-VHA costs, patient and provider satisfaction, medication compliance, and diagnosis specific outcomes.
| Condition | Treatment or Intervention |
|---|---|
| Major Depressive Disorder Post-Traumatic Stress Disorders Anxiety Disorders | Procedure: Telephone care |
MedlinePlus related topics: Anxiety; Mental Health; Post-Traumatic Stress Disorder
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Expected Total Enrollment: 350
Study start: October 2003; Expected completion: September 2008
Eligibility
Genders Eligible for Study: Both
Criteria
Patients will be eligible for this study if they:
- Carry a diagnosis of major depression, post-traumatic stress disorder (PTSD), or non-PTSD anxiety disorders
- Are psychiatrically stable subjects with a Global Assessment of Functioning scale score of >50
- Do not have psychiatric hospitalizations in the previous six months
- Do not have active substance abuse disorders
Location and Contact Information
Vermont
VA Medical & Regional Office Center, White River Junction, Vermont, 05009-0001, United States; Recruiting
VA Medical & Regional Office Center, White River, White River Junction, Vermont, 05009-0001, United States; Recruiting
More Information
Record last reviewed: March 2005
Last Updated: March 17, 2005
Record first received: March 17, 2005
ClinicalTrials.gov Identifier: NCT00105885
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- Anxiety Disorders (National Institute of Mental Health)
- Anxiety Disorders (National Institute of Mental Health)

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