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NCT02648022 · ClinicalTrials.gov registry record · NA

Integrated Care for Patients With High Risk Substance Use and Psychiatric Disorder With Chronic Direct Acting Antiviral Treatment

A NA study, sponsored by VA Office of Research and Development.

Completed
Registry status
NA
Development phase
83
Enrollment target

NCT02648022: Completed NA study, sponsored by VA Office of Research and Development.

NCT02648022 is a NA study that has completed, run by VA Office of Research and Development. The registered enrollment target is 83 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT02648022, a NA study, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
NA
Development phase
83 participants
Enrollment target

Study Summary

To determine the effect of an integrated care protocol on antiviral treatment and sustained virologic response (SVR) rates following initiation of direct acting antiviral therapies (DAA) treatments in 2011.

Primary Outcome

The primary outcome for the study was the proportion of patients that achieve an SVR. Patient adherence to completing the prescribed therapy and SVR were both tracked with medical records. Viral load at 4, 12-and 24-weeks during treatment initiation have been shown to predict final SVR. Final SVR data consists of viral tests conducted at 6 months after the termination of therapy.

Interventions

  • BEHAVIORAL Brief mental health interventions and case management

Trial Details

FieldValue
Enrollment Target 83 participants
Start Date 2012-01
Est. Completion 2014-02
Phase NA
VA Office of Research and Development

1,668 total trials

What the finished NCT02648022 record still lists

NCT02648022 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 83 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 1 intervention - of which Brief mental health interventions and case management is the first listed.

NCT02648022 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02648022 about?

NCT02648022 is a clinical study titled "Integrated Care for Patients With High Risk Substance Use and Psychiatric Disorder With Chronic Direct Acting Antiviral Treatment". To determine the effect of an integrated care protocol on antiviral treatment and sustained virologic response (SVR) rates following initiation of direct acting antiviral therapies (DAA) treatments in 2011.

What is the current status of trial NCT02648022?

This trial is currently completed. It is a NA study. The enrollment target is 83 participants. The study started on 2012-01. Estimated completion is 2014-02.

What interventions are being tested in trial NCT02648022?

The interventions under investigation include: Brief mental health interventions and case management (BEHAVIORAL).

Who is sponsoring clinical trial NCT02648022?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02648022's enrollment target sits among peer trials

83 990th of 2000 higher than 1,011 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02648022, the US trial registry maintained by the National Library of Medicine. NCT02648022 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.