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NCT01286311 · ClinicalTrials.gov registry record · NA

Tailored Communication to Reduce Cardiovascular Risk

A NA study, sponsored by Northwestern University.

Completed
Registry status
NA
Development phase
464
Enrollment target

NCT01286311: Completed NA study, sponsored by Northwestern University.

NCT01286311 is a NA study that has completed, run by Northwestern University. The registered enrollment target is 464 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01286311, a NA study, has completed, sponsored by Northwestern University.

COMPLETED
Registry status
NA
Development phase
464 participants
Enrollment target

Study Summary

The primary goal of the trial is to test the feasibility and efficacy of a cardiovascular disease quality improvement system that couples EMR-based patient identification with individually tailored patient messages. The study will test the hypothesis that that a tailored patient-directed approach to cardiovascular risk reduction integrated into patients' primary care delivery site will improve control of elevated low-density lipoprotein cholesterol and other card iac risk factors more than routine care alone for patients at intermediate or high risk for cardiovascular disease.

Primary Outcome

Significant LDL cholesterol reduction at 9 months Definition: Percentage of patients with LDL-C repeated and which is at least 30 mg/dl lower than baseline

Interventions

  • BEHAVIORAL Direct-to-patient tailored cardiovascular risk message system

Trial Details

FieldValue
Enrollment Target 464 participants
Start Date 2011-01
Est. Completion 2013-01
Phase NA
Northwestern University

1,209 total trials

What the finished NCT01286311 record still lists

NCT01286311 is an interventional study that assigns participants to a tested intervention. The registered 464 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 1 intervention - of which Direct-to-patient tailored cardiovascular risk message system is the first listed.

NCT01286311 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01286311 about?

NCT01286311 is a clinical study titled "Tailored Communication to Reduce Cardiovascular Risk". The primary goal of the trial is to test the feasibility and efficacy of a cardiovascular disease quality improvement system that couples EMR-based patient identification with individually tailored patient messages. The study will test the hypothesis that that a tailored patient-directed approach to...

What is the current status of trial NCT01286311?

This trial is currently completed. It is a NA study. The enrollment target is 464 participants. The study started on 2011-01. Estimated completion is 2013-01.

What interventions are being tested in trial NCT01286311?

The interventions under investigation include: Direct-to-patient tailored cardiovascular risk message system (BEHAVIORAL).

Who is sponsoring clinical trial NCT01286311?

This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01286311's enrollment target sits among peer trials

464 222nd of 2000 higher than 1,779 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 NCT01286311, the US trial registry maintained by the National Library of Medicine. NCT01286311 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.