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COMPLETED NA

Impact of Teledermatology on Health Services Outcomes in the Department of Veterans Affairs

NCT00488293 · View on ClinicalTrials.gov ↗

Study Summary

This study compares store and forward teledermatology with the conventional clinic-based consult process. Our primary objective is to determine whether the mean change in quality of life, as rated by the subscale scores and composite score on the Skindex-16 differs between the store and forward and conventional care modalities.

Interventions

  • PROCEDURE Store and forward teledermatology

Study Locations (2)

Minnesota

  • Minneapolis VA Health Care System, Minneapolis, MN — Minneapolis

Missouri

  • Harry S. Truman Memorial, Columbia, MO — Columbia

Trial Details

FieldValue
Enrollment Target 392 participants
Start Date 2008-11
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 NCT00488293

The ClinicalTrials.gov registry entry for NCT00488293 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 392 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 Quality of Life appearing as the primary indexed condition, and to 1 intervention — of which Store and forward teledermatology 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: NCT00488293 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Minnesota, Missouri. 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 NCT00488293 about?

NCT00488293 is a clinical study titled "Impact of Teledermatology on Health Services Outcomes in the Department of Veterans Affairs". This study compares store and forward teledermatology with the conventional clinic-based consult process. Our primary objective is to determine whether the mean change in quality of life, as rated by the subscale scores and composite score on the Skindex-16 differs between the store and forward and ...

What is the current status of trial NCT00488293?

This trial is currently completed. It is a NA study. The enrollment target is 392 participants. The study started on 2008-11. Estimated completion is 2011-06.

What conditions does trial NCT00488293 study?

This clinical trial studies the following conditions: Quality of Life, Telemedicine, Skin Diseases. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00488293?

The interventions under investigation include: Store and forward teledermatology (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00488293?

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 NCT00488293 being conducted?

This trial has 2 study locations across Minnesota, Missouri. 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