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Telepsychology-Service Delivery for Depressed Elderly Veterans
This study is currently recruiting participants.
Verified by Department of Veterans Affairs, August 2009
First Received: May 9, 2006   Last Updated: August 24, 2009   History of Changes
Sponsors and Collaborators: Department of Veterans Affairs
Medical University of South Carolina
University of Maryland
Information provided by: Department of Veterans Affairs
ClinicalTrials.gov Identifier: NCT00324701
  Purpose

The purpose of this study is to see whether therapy for elderly adults with major depression can be delivered effectively using videoconferencing technology ("telepsychology"), which allows a therapist and patient who are not in the same room as one another to communicate. We are interested in learning if this form of mental health service delivery is an acceptable alternative to traditional face-to-face therapy delivered with the therapist in the same room as the patient.


Condition Intervention
Depression
Aged
Behavioral: Telepsychology
Behavioral: Face-to-face therapy

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Telepsychology-Service Delivery for Depressed Elderly Veterans

Resource links provided by NLM:


Further study details as provided by Department of Veterans Affairs:

Primary Outcome Measures:
  • Is in-home telepsychology for major depressive disorder in older adults as effective as same-room treatment on clinical and process outcomes? Is in-home telepsychology for major depressive disorder in older adults cost-effective? [ Time Frame: Outcome measured assessed at post treatment ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • The ultimate objective is to obtain information on whether telepsychology is an acceptable and effective alternative to traditional face-to-face mental health treatment for elderly veterans living in rural areas, many of whom are minorities. [ Time Frame: Outcome measured assessed at post treatment ] [ Designated as safety issue: No ]

Estimated Enrollment: 224
Study Start Date: September 2006
Estimated Study Completion Date: June 2010
Estimated Primary Completion Date: June 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1 Behavioral: Telepsychology
therapy done at patients house
Behavioral: Face-to-face therapy
therapy delivered at the VAMC

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   60 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Participants will be older male and female veterans,
  • age 60 and above,
  • with diagnoses of major depressive disorder (MDD) assigned on the basis of the Structured Clinical Interview for DSM-IV (SCID; Spitzer et al., 1997).

Exclusion Criteria:

  • Actively psychotic or demented persons,
  • individuals with both suicidal ideation and clear intent, and
  • individuals meeting criteria for substance dependence will be excluded from participation.

However, in order to maximize generalization of results, presence of other forms of psychopathology will not be a basis for exclusion. All of these structured interviews will be audiotaped in order to calculate inter-rater reliability on a randomly selected 20%. (See Human Subjects for procedures in place for suicidal participants or potential participants).

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00324701

Contacts
Contact: Sarah A Jackson, BA MA (843) 789-7587 sarah.jackson@va.gov
Contact: Melissa L Koerner, BA MSW

Locations
United States, South Carolina
Ralph H Johnson VA Medical Center, Charleston Recruiting
Charleston, South Carolina, United States, 29401-5799
Contact: Leonard E Egede, MD MS     (843) 789-6670     egedel@musc.edu    
Contact: Sarah A Jackson, BA MA     (843) 789-7587     sarah.jackson@va.gov    
Principal Investigator: Leonard E. Egede, MD MS            
Sub-Investigator: Bartley Christopher Frueh, PhD            
Sub-Investigator: Patrick D Mauldin, PhD MA BS            
Sub-Investigator: Rebecca Grant Knapp, BS MS PhD            
Sub-Investigator: Ronald E. Acierno, PhD MS BA            
Sub-Investigator: Charles Ellis, BS MA PhD            
Sub-Investigator: Carl W Lejuez, PhD MA BA            
Sponsors and Collaborators
Medical University of South Carolina
University of Maryland
Investigators
Principal Investigator: Leonard E. Egede, MD MS Ralph H Johnson VA Medical Center, Charleston
  More Information

No publications provided by Department of Veterans Affairs

Additional publications automatically indexed to this study by National Clinical Trials Identifier (NCT ID):
Responsible Party: Department of Veterans Affairs ( Egede, Leonard - Principal Investigator )
Study ID Numbers: IIR 04-421, HR16402
Study First Received: May 9, 2006
Last Updated: August 24, 2009
ClinicalTrials.gov Identifier: NCT00324701     History of Changes
Health Authority: United States: Federal Government

Keywords provided by Department of Veterans Affairs:
Mental Health
Geriatric Medicine
Depression
Health Service Delivery
Aged

Study placed in the following topic categories:
Depression
Mental Disorders
Mood Disorders
Depressive Disorder
Behavioral Symptoms

Additional relevant MeSH terms:
Depression
Mental Disorders
Mood Disorders
Depressive Disorder
Behavioral Symptoms

ClinicalTrials.gov processed this record on September 01, 2009