- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01207180
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
Status
Completed
Conditions
Intervention / Treatment
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.
Clinical Trials on Patient Discharge
-
Rush University Medical CenterCompletedPatient Discharge | Patient AdmissionUnited States
-
Rush University Medical CenterCompletedPatient Discharge | Patient AdmissionUnited States
-
Virginia MoyerAgency for Healthcare Research and Quality (AHRQ)CompletedPatient DischargeUnited States
-
Hackensack Meridian HealthWithdrawn
-
Cambridge Health AllianceCompletedPatient DischargeUnited States
-
Medical College of WisconsinUniversity of Wisconsin, Milwaukee; Children's Hospital and Health System Foundation... and other collaboratorsCompletedPatient DischargeUnited States
-
KU LeuvenCompletedPatient Discharge | Pharmacist | Physicians, Primary CareBelgium
-
Azienda Ospedaliera Città della Salute e della...Completed
-
Unity Health TorontoCompletedContinuity of Patient Care | Patient Discharge | Medical Records Systems, Computerized | Hospital Information SystemsCanada
-
University of AarhusCompletedPatient DischargeDenmark
Clinical Trials on Phone call follow-up
-
Cedars-Sinai Medical CenterRecruiting
-
Université de SherbrookeMinistère de l'Économie, de la Science et de l'InnovationCompletedRehabilitation | Orthopedic DisorderCanada
-
University Hospital, ToulouseCompleted
-
The Cleveland ClinicCompletedAbnormal Uterine BleedingUnited States
-
Winnipeg Regional Health AuthorityPrimary Supervisor: Dr. James Bolton MD FRCPCUnknownSuicidal Ideation | Suicide, Attempted | Suicide | Suicide and Self-harm | Suicide GestureCanada
-
Vanderbilt University Medical CenterCompleted
-
Assistance Publique - Hôpitaux de ParisRecruiting
-
Glasgow Royal InfirmaryGlasgow Caledonian UniversityUnknown
-
Saint Anselm CollegeCatholic Medical CenterCompletedDepression, PostpartumUnited States
-
Rennes University HospitalCompletedRecurrent Anterior Shoulder InstabilityFrance