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NCT00611091 · ClinicalTrials.gov registry record · NA
Improving Posthospital Medication Management of Older Adults Through Health IT
A NA study, sponsored by University of Massachusetts, Worcester.
- Completed
- Registry status
- NA
- Development phase
- 5,077
- Enrollment target
NCT00611091 is a NA study that has completed, run by University of Massachusetts, Worcester. The registered enrollment target is 5,077 participants.
The verdict
NCT00611091, a NA study, has completed, sponsored by University of Massachusetts, Worcester.
- COMPLETED
- Registry status
- NA
- Development phase
- 5,077 participants
- Enrollment target
Study Summary
The incidence of drug-induced injury is high in the ambulatory geriatric population and is increased for elders upon transition from the hospital to the ambulatory setting. In this application, we describe an effort to build on our extensive experience in medication safety and HIT-based medication management to respond to the AHRQ RFA entitled Ambulatory Safety and Quality Program: Improving Quality through Clinician Use of Health IT (RFA-HS-07-006). In this study, we propose to develop and evaluate the value of an enhanced, HIT-based transitional care intervention superimposed on the ambulatory electronic medical record (EMR) to improve the quality and safety of medication management, focusing particularly on the transition from the inpatient to the ambulatory setting for older adults with multiple comorbid conditions who are prescribed high risk medications. We propose a randomized controlled trial of a HIT-based transitional care intervention with enhanced medication and therapeutic monitoring alerts to improve the quality and safety of patient monitoring and medication management. We postulate that the efficient and coordinated delivery of actionable health information to the clinician via use of HIT in the ambulatory setting can improve medication safety for the growing geriatric population. The specific aims for this study are to evaluate, among a population of older adults discharged from the hospital, the impact of an enhanced discharge information system initiated upon transition to the ambulatory setting: (1) on the rate of follow-up by an outpatient provider within 14 days of hospital discharge; (2) on the prevalence of appropriate monitoring for selected high risk medications at 30 days from the time of hospital discharge; (3) on the incidence of adverse drug events (ADEs) 30 days after discharge; and (4) on the rate of emergency department visits and hospital readmission within 30 days of discharge. A secondary aim for this study is to determine costs d
Interventions
- OTHER Electronic delivery of enhanced discharge information to the ambulatory physician
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5,077 participants |
| Start Date | 2010-08 |
| Est. Completion | 2013-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00611091
The ClinicalTrials.gov registry entry for NCT00611091 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 5,077 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Massachusetts, Worcester, which has 240 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Electronic delivery of enhanced discharge information to the ambulatory physician is the first listed.
NCT00611091 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00611091 about?
NCT00611091 is a clinical study titled "Improving Posthospital Medication Management of Older Adults Through Health IT". The incidence of drug-induced injury is high in the ambulatory geriatric population and is increased for elders upon transition from the hospital to the ambulatory setting. In this application, we describe an effort to build on our extensive experience in medication safety and HIT-based medication m...
What is the current status of trial NCT00611091?
This trial is currently completed. It is a NA study. The enrollment target is 5,077 participants. The study started on 2010-08. Estimated completion is 2013-09.
What interventions are being tested in trial NCT00611091?
The interventions under investigation include: Electronic delivery of enhanced discharge information to the ambulatory physician (OTHER).
Who is sponsoring clinical trial NCT00611091?
This trial is sponsored by University of Massachusetts, Worcester, which has 240 total clinical trials registered on ClinicalTrials.gov.
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