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Efficacy of Telepsychiatry in the Treatment of Depression
This study has been completed.
Study NCT00012610   Information provided by Department of Veterans Affairs
First Received: March 14, 2001   Last Updated: May 11, 2009   History of Changes

March 14, 2001
May 11, 2009
 
 
 
 
Complete list of historical versions of study NCT00012610 on ClinicalTrials.gov Archive Site
 
 
 
Efficacy of Telepsychiatry in the Treatment of Depression
Efficacy of Telepsychiatry in the Treatment of Depression

Telepsychiatry is a novel means of providing expert psychiatric treatment to patients who live far from a source of care. If it can be demonstrated that treatment via telepsychiatry is as effective as in-person treatment, then many individuals with psychiatric illness will have easy access to psychiatric care, even if they live in geographically remote areas.

Background:

Telepsychiatry is a novel means of providing expert psychiatric treatment to patients who live far from a source of care. If it can be demonstrated that treatment via telepsychiatry is as effective as in-person treatment, then many individuals with psychiatric illness will have easy access to psychiatric care, even if they live in geographically remote areas.

Objectives:

The major goal of this study was to determine whether treatment of depressive disorders via telepsychiatry is as effective as in-person treatment. In addition, this study was designed to determine if depressed patients are as compliant and as satisfied with telepsychiatry as with in-person treatment. Another goal was to compare the cost and cost-effectiveness of remote treatment via telepsychiatry to in-person treatment.

Methods:

In this randomized controlled trial, veterans who presented with depression to any of three VA Maryland Health Care facilities with a SCID-IV depression diagnosis and a Hamilton Rating Scale for Depression (Ham-D) score of 16 or above were eligible for participation. Eligible veterans were randomized to either "in-person" treatment or "remote" treatment. Treatment occurred over six months and consisted of psychotropic medication and psycho-education concerning the disease, medications, and side effects. The major outcome variables included changes in Ham-D depression ratings and Beck Depression Inventory (BDI) self-reported depression ratings.

Status:

Completed.

 
Interventional
Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Depression
Procedure: Telepsychiatry
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
119
September 2000
 

Inclusion Criteria:

Depression, Hamilton 16 or above, SCID-IV depression diagnosis

Exclusion Criteria:

Both
 
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00012610
Ruskin, Paul - Principal Investigator, Department of Veterans Affairs
ACC 97-034
Department of Veterans Affairs
 
Principal Investigator: Paul E. Ruskin, MD VA Maryland Health Care System, Baltimore
Department of Veterans Affairs
March 2001

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP