Status:

COMPLETED

Design & Evaluation of a Medication Therapy Management Program to Improve Patient Safety in Medicare Beneficiaries

Lead Sponsor:

University of Illinois at Chicago

Collaborating Sponsors:

Agency for Healthcare Research and Quality (AHRQ)

Duke University

Conditions:

Chronic Illness

Adverse Effects

Eligibility:

All Genders

65+ years

Phase:

NA

Brief Summary

The purpose of this study is to determine if a medication therapy management program designed to reconcile a patient's medications and identify and resolve drug related problems can reduce adverse dru...

Detailed Description

This study will be a multicenter, prospective, randomized study of usual care (Arm 1; control group) compared with usual care plus medication reconciliation by patient interview and a drug related pro...

Eligibility Criteria

Inclusion

  • Be at least 65 years old at enrollment
  • Primarily uses English language for written and oral communication
  • Have three or more comorbid conditions associated with increased healthcare utilization (Diabetes Mellitus, Congestive Heart Failure, Asthma, Hypertension, Dyslipidemia, COPD, Coronary Artery Disease, Chronic Renal Failure, Arthritis, Depression, Dementia, Chronic Pain, Conditions requiring anticoagulation with warfarin)
  • Have visited a physician at one or more of the clinics on a regular basis (defined as two or more clinic visits over one year prior to the study start) for these conditions
  • Have received 6 or more different chronic prescription medications over the six months prior to the enrollment period
  • Have a telephone line and agree to maintain it for at least six months
  • Have one of the following situations placing him/her at risk for a DRP (Any ER visit in past 30 days or Urgent Care visit in past 30 days leading to a change in medication or change in medication dose; New physician visit in past 30 days; Hospitalization in past 30 days; Invasive procedure (a procedure requiring substantive changes to medication taking practices or which requires informed consent) in past 30 days; Change in medication in past 30 days; Three or more providers seen in the past year

Exclusion

  • Terminal condition, where life expectancy is less than 6 months
  • Patients already enrolled in an MTM program where medication reconciliation and/or assessment of DRPs has occurred in the previous 12 months

Key Trial Info

Start Date :

November 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

January 1 2010

Estimated Enrollment :

637 Patients enrolled

Trial Details

Trial ID

NCT00773942

Start Date

November 1 2007

End Date

January 1 2010

Last Update

July 24 2019

Active Locations (3)

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Page 1 of 1 (3 locations)

1

University of Illinois at Chicago

Chicago, Illinois, United States, 60612

2

Duke University Health System

Durham, North Carolina, United States, 27705

3

Baylor Health Care System

Dallas, Texas, United States, 75206