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COMPLETED NA

The Effectiveness of FMPO in Improving the Quality of Care for Persons With Severe Mental Illness.

NCT00466323 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to learn how to help veterans play a stronger role in shaping their mental health care. Specifically we want to see if we can help veterans improve their mental health treatment by helping them decide if they want to involve family in their mental health treatment, and if so, how. The study will compare a "family member provider" program to an "enhanced treatment as usual approach" in achieving these goals.

Interventions

  • BEHAVIORAL Family Member Provider Outreach
  • BEHAVIORAL Enhanced treatment as usual (e-TAU)

Study Locations (2)

California

  • VA Greater Los Angeles Healthcare System, West Los Angeles, CA — West Los Angeles

Maryland

  • Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD — Baltimore

Trial Details

FieldValue
Enrollment Target 238 participants
Start Date 2007-09
Est. Completion 2011-06
Phase NA

Sponsor

US Department of Veterans Affairs

158 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00466323

The ClinicalTrials.gov registry entry for NCT00466323 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 238 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is US Department of Veterans Affairs, which has 158 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Schizophrenia appearing as the primary indexed condition, and to 2 interventions — of which Family Member Provider Outreach is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00466323 reports 2 study locations spanning 2 distinct geographic areas — top geographies include California, Maryland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00466323 about?

NCT00466323 is a clinical study titled "The Effectiveness of FMPO in Improving the Quality of Care for Persons With Severe Mental Illness.". The purpose of this study is to learn how to help veterans play a stronger role in shaping their mental health care. Specifically we want to see if we can help veterans improve their mental health treatment by helping them decide if they want to involve family in their mental health treatment, and i...

What is the current status of trial NCT00466323?

This trial is currently completed. It is a NA study. The enrollment target is 238 participants. The study started on 2007-09. Estimated completion is 2011-06.

What conditions does trial NCT00466323 study?

This clinical trial studies the following conditions: Schizophrenia, Schizoaffective Disorder, Major Depression. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00466323?

The interventions under investigation include: Family Member Provider Outreach (BEHAVIORAL), Enhanced treatment as usual (e-TAU) (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00466323?

This trial is sponsored by US Department of Veterans Affairs, which has 158 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00466323 being conducted?

This trial has 2 study locations across California, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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