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NCT01158001 · ClinicalTrials.gov registry record · NA

Telemedicine for Improved Delivery of Psychosocial Treatments for Post Traumatic Stress Disorder

A NA study of Depression and Anxiety, sponsored by Veterans Medical Research Foundation.

Completed
Registry status
NA
Development phase
211
Enrollment target
1
Study location

NCT01158001 is a NA study of Depression and Anxiety that has completed, run by Veterans Medical Research Foundation. The registered enrollment target is 211 participants, below the 786-participant average among 679 other Depression trials with a reported enrollment target (73% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01158001, a NA study of Depression and Anxiety, has completed, sponsored by Veterans Medical Research Foundation.

COMPLETED
Registry status
NA
Development phase
211 participants
Enrollment target
1
Study location

Study Summary

The objective of the proposed study is to conduct a systematic comparison of post traumatic stress disorder (PTSD) outcomes for veterans receiving exposure therapy via telemedicine versus in-person care. The primary aim is to determine feasibility: whether telemedicine can be used as a tool to extend effective, specialized mental health services, such as Prolonged Exposure therapy (PE; a therapy designed to help clients face fears related to a traumatic event), to veterans with limited access to care. A secondary aim is to determine if therapy delivered by telemedicine affects the quality of care in terms of clinical outcomes and the quality of patient-therapist interaction. A tertiary aim is to examine whether results from neuropsychological testing predict treatment outcomes.

Interventions

  • BEHAVIORAL Prolonged exposure therapy

Study Locations (1)

California

  • VA San Diego Healthcare System - San Diego

Trial Details

FieldValue
Enrollment Target 211 participants
Start Date 2009-05
Est. Completion 2012-09
Phase NA

What the Registry Record Tells You About NCT01158001

The ClinicalTrials.gov registry entry for NCT01158001 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 211 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 786-participant average among 679 other Depression trials with a reported enrollment target (73% lower). The listed sponsor is Veterans Medical Research Foundation, which has 35 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Depression appearing as the primary indexed condition, and to 1 intervention - of which Prolonged exposure therapy is the first listed.

NCT01158001 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT01158001 about?

NCT01158001 is a clinical study titled "Telemedicine for Improved Delivery of Psychosocial Treatments for Post Traumatic Stress Disorder". The objective of the proposed study is to conduct a systematic comparison of post traumatic stress disorder (PTSD) outcomes for veterans receiving exposure therapy via telemedicine versus in-person care. The primary aim is to determine feasibility: whether telemedicine can be used as a tool to exten...

What is the current status of trial NCT01158001?

This trial is currently completed. It is a NA study. The enrollment target is 211 participants. The study started on 2009-05. Estimated completion is 2012-09.

What conditions does trial NCT01158001 study?

This clinical trial studies the following conditions: Depression, Anxiety, Posttraumatic Stress Disorders.

What interventions are being tested in trial NCT01158001?

The interventions under investigation include: Prolonged exposure therapy (BEHAVIORAL).

Who is sponsoring clinical trial NCT01158001?

This trial is sponsored by Veterans Medical Research Foundation, which has 35 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01158001 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.