Discharge Planning for Elderly Patients in the Emergency Department: Use of a Brief Phone Call After Discharge to Improve Medication Utilization and Physician Follow-up

November 17, 2011 updated by: Kevin Biese, MD, University of North Carolina, Chapel Hill
The investigators hypothesize that the acquisition and correct utilization of medications as well as arranging and attending follow-up appointments will improve as a result of a phone call intervention 1-3 days after elderly patients are discharged from the emergency department (ED).

Study Overview

Detailed Description

Older patients seen in the ED are at high risk of functional decline and return visits to the ED. Previous studies have shown that a comprehensive assessment by a geriatric specialist at the time of discharge from the ED along with extensive integration with home services and/or referral to community services can decrease functional decline and return visits to the ED as well as increase patient satisfaction, but this intervention is resource intensive requiring a geriatric discharge specialist to be available to the emergency department 24 hours a day/ 7 days a week. It is also known that in other patient populations telephone reminders to make follow up appointments can increase rate of follow up and that comprehension of discharge instructions is the primary barrier to compliance with discharge instructions. It has been shown that telephone follow-up interviews are feasible for geriatric patients discharged from the ED, and that many elderly patients discharged from the ED do not understand their discharge instructions or attend follow-up appointments. However, there are no published studies evaluating whether a follow up telephone call after discharge from the ED can improve patient compliance with the medical treatment plan including obtaining follow - up appointments and obtaining prescribed medications as well as using them appropriately. We seek to determine if we can increase compliance with medications and outpatient follow up with a phone call from a nurse provider 1-3 days after discharge.

Study Type

Interventional

Enrollment (Actual)

157

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • North Carolina
      • Chapel Hill, North Carolina, United States, 27599
        • University of North Carolina Emergency Department

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

63 years and older (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Age 65 or over
  • Discharged from the UNC emergency department

Exclusion Criteria:

  • In the hospital at the time of phone call follow-up
  • Neither the patient nor their responsible party are able to pass a standardized test to assess cognitive function

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Follow-up phone call from Nurse
Patients in this are will receive a phone call follow-up from a nurse 1-3 days after their discharge from the ED.
A nurse will call the patient to counsel patients on their medications and following up with their primary care provider.
Placebo Comparator: Satisfaction survey
This group of patients will receive a phone call from a student who will conduct a brief satisfaction survey of the patient's experience in the ED.
Patients will be given a satisfaction survey.
Placebo Comparator: Control group
Patients in this group will receive no phone call at 1-3 days.
Control group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Whether patient obtained medications prescribed at their discharge from ED
Time Frame: 5-8 days after discharge from ED
5-8 days after discharge from ED
Whether patient is using medications that were prescribed at their ED discharge correctly
Time Frame: 5-8 days after discharge from ED
5-8 days after discharge from ED
Whether the patient arranged a follow-up appointment with their primary care provider
Time Frame: 5-8 days after discharge from ED
5-8 days after discharge from ED
Whether patient attended visit with their primary care provider after discharge from the ED
Time Frame: 30-35 days after discharge from ED
30-35 days after discharge from ED

Secondary Outcome Measures

Outcome Measure
Time Frame
Patient's satisfaction with ED visit
Time Frame: 5-8 days after discharge from the ED
5-8 days after discharge from the ED
Return to the ED within 30 days of initial visit
Time Frame: 30-35 days after discharge from ED
30-35 days after discharge from ED
Cost of the intervention
Time Frame: 35 days after last patient enrolled
35 days after last patient enrolled

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Kevin J Biese, MD, University of North Carolina, Chapel Hill

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2010

Primary Completion (Actual)

November 1, 2010

Study Completion (Actual)

November 1, 2010

Study Registration Dates

First Submitted

September 13, 2010

First Submitted That Met QC Criteria

September 21, 2010

First Posted (Estimate)

September 22, 2010

Study Record Updates

Last Update Posted (Estimate)

November 18, 2011

Last Update Submitted That Met QC Criteria

November 17, 2011

Last Verified

November 1, 2011

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 10-0978

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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