Feasibility of Using a Telemedicine Medication Delivery Unit for Older Adults

Not Applicable

Withdrawn

• Conditions: Adverse Reaction to Drug; Medication Adherence; Medication Nonadherence
• Interventions: Device: Computerized medication delivery unit (Electronic Medication Management Assistant (EMMA)

• Registration Number: NCT01430702
• Lead Sponsor: University of Pittsburgh

Brief Summary

Care transition interventions have been successful in reducing medication-related problems and associated rehospitalization primarily by focusing on medication reconciliation conducted by trained healthcare professionals. Programs to improve the medication reconciliation process have largely been effective, but have limitations including the expense associated with recruiting, training, and retaining care transition healthcare professionals (e.g., nurses and nurse practitioners) the ability to provide services within a finite geographic area, and the retrospective nature of the reconciliation process which usually occurs in the home following hospital discharge. Our short-term objective is to use Pennsylvania Department of Aging resources to assess the feasibility of using a telemedicine medication delivery unit for frail older adults that require medication assistance in their home immediately following an acute hospitalization. As part of this feasibility assessment, the investigators will assess (1) recruitment process and procedures, (2) data collection procedures, (3) resource utilization, (4) drop-out rates, (5) acceptability and usability of the EMMA® telemedicine medication delivery unit, (6) medication adherence, and (7) medication-reconciliation errors during transition from hospital to home.

Detailed Description

Care transition interventions have been successful in reducing medication-related problems and associated re-hospitalization primarily by focusing on medication reconciliation conducted by trained healthcare professionals. Medication reconciliation is the process of identifying discrepancies in drug regimens prescribed in different care settings or at different time points within the same setting, to inform prescribing decisions and prevent medication-related problems, including medication errors (MEs) and adverse drug events (ADEs). MEs and ADEs are particularly common during and following hospitalization, when multiple changes to a patients' medication regimens may be accompanied by inadequate patient education,\\ follow-up, and continuity of care with primary care physicians and case managers. As a result of these problems, as many as 42% of general medical patients experience an ME or ADE after hospital discharge, with disproportionate impacts on older adults with chronic medical conditions. Post-hospital ADEs can be expensive, as12% result in an emergency department evaluation and 5% in readmission, which is associated with a significant increase in healthcare resource utilization and further fragmentation in care.

Programs to improve the medication reconciliation process have largely been effective, but have limitations including the expense associated with recruiting, training, and retaining care transition healthcare professionals (e.g., nurses and nurse practitioners), the ability to provide services within a finite geographic area, and the retrospective nature of the reconciliation process, which usually occurs in the home following hospital discharge. The investigators short-term objective is to use Pennsylvania Department of Aging resources to assess the feasibility of using a telemedicine medication delivery unit for frail older adults that require medication assistance in their home immediately following an acute hospitalization. As part of this feasibility assessment, the investigators will assess several methods and intervention-related components.

Study Timeline

• Study Start: 2011-09
• Study First Submitted: 2011-09-01
• Study First Submitted QC: 2011-09-07
• Study First Posted: 2011-09-08
• Primary Completion: 2011-12
• Study Completion: 2012-04
• Status Verified: 2013-01
• Last Update Submitted: 2013-01-14
• Last Update Posted: 2013-01-16

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Patients > 65 years of age.
• Admitted during the study period for a nonpsychiatric condition to UPMC Presbyterian Hospital.
• Documented in their medical record at least 1 of 11 diagnoses, including: stroke, congestive heart failure, coronary artery disease, cardiac arrhythmias, chronic obstructive pulmonary disease, diabetes mellitus, spinal stenosis, hip fracture, peripheral vascular disease, deep venous thrombosis, and pulmonary embolism.
• Prescribed > 5 and < 20 regularly scheduled (i.e., non-PRN) prescription medications.
• Be from and return to a home setting (not assisted living, skilled nursing, program for all-inclusive care of the elderly, etc).
• Reside within a predefined geographic radius (i.e., Allegheny, Beaver, Butler, Fayette, Washington or Westmoreland Counties) of the hospital.
• Have a working telephone.
• Be English speaking.
• Have an informal caregiver or support person.

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Exclusion Criteria

• Have an active prescription for narcotic analgesic.
• Enrolled in or plan to enroll into hospice.
• Plans to travel in the next 30 days.
• Participating in another research protocol.
• Have evidence in the chart of a diagnosis of active delirium.
• Have evidence in the chart of a diagnosis of dementia.
• Have evidence in the chart of legal blindness.
• Unable to demonstrate appropriate use of the EMMA medication delivery unit.
• Unable to receive ATT wireless services data plan based on physical address.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Computerized medication delivery unit	Computerized medication delivery unit (Electronic Medication Management Assistant (EMMA)	Those hospitalized patients that meet all inclusion and exclusion criteria will be provided with a computerized medication delivery unit for use in their homes for the 30-day period following discharge.

Primary Outcome Measures

Name	Time	Method
medication adherence	30-day	The investigators will assess adherence by determining the number of regularly scheduled medications taken vs. prescribed (data will come from the EMMA® Report software).

Secondary Outcome Measures

Name	Time	Method
acceptability and usability of the EMMA® telemedicine medication delivery unit	30-day	The investigators will assess acceptability and usability of the EMMA® telemedicine medication delivery unit through a previously validated instrument developed by the The Quality of Life Technology (QoLT) Center at Carnegie Mellon University.
medication-reconciliation errors during transition from hospital to home	30-day	Finally, the investigators will measure medication-reconciliation errors using the Medication Discrepancy Tool (MDT).

Trial Locations

Locations (1)

UPMC Presbyterian Hospital; 🇺🇸 Pittsburgh, Pennsylvania, United States