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Telephone Care as a Substitute for Routine Psychiatric Medication Management - Article


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Developmental Disabilities & Disorders

Developmental Disabilities




Clinical Trial: Telephone Care as a Substitute for Routine Psychiatric Medication Management

This study is currently recruiting patients.

Sponsored by: Department of Veterans Affairs
Information provided by: Department of Veterans Affairs

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

Further Study Details: 
Primary Outcomes: Total VHA health services utilization; Mental health component scores from the SF-12-V
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
William B. Weeks, MD MBA  802-291-6285    william.weeks@med.va.gov 

      VA Medical & Regional Office Center, White River, White River Junction,  Vermont,  05009-0001,  United States; Recruiting
Amy E. Wallace, MD  802-295-9363  Ext. 5680    Amy.Wallace@med.va.gov 

More Information

Study ID Numbers:  TEL 01-146
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

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December 4, 2008



Page Updated: September 6, 2005
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