- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02117804
Early Screen for Discharge Planning in Community Hospitals
May 20, 2015 updated by: Diane Holland, Mayo Clinic
Validating Discharge Planning Decision Support in a Regional Community Hospital
The purpose of this study is to determine the predictive performance of the Early Screen for Discharge Planning (ESDP) tool in a regional community hospital.
The central hypothesis is that the ESDP differentiates between patients in a regional community hospital who would benefit from those who would not benefit from early discharge-planning intervention as measured by problems and unmet continuing care needs, quality of life, length of stay, and referrals to post-acute services.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Patients who are hospitalized for medical or surgical reasons who consent to the study will be screened within 24 hours of hospital admission using the Early Screen for Discharge Planning (ESDP).
The ESDP is a four-item screening tool used to determine on admission which patients are likely to have complex discharge plans and could benefit from early engagement of discharge planning personnel.
The ESDP yields a total score, and those with a score of 10 or greater are considered to have a "high score" and likely to have a complex discharge plan.
Those with a score of 9 or below have a "low score".
The ESDP screen has been proven to be valid in large academic medical centers.
This study will determine if the screen performs with the same validity in a small community hospital.
Study Type
Observational
Enrollment (Actual)
225
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
-
-
Wisconsin
-
Eau Claire, Wisconsin, United States, 54703
- Mayo Clinic Health System - Eau Claire
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The study targets adults hospitalized for a variety of medical and surgical conditions in a rural regional community hospital that is part of a large health system in the Midwest.
The sample will be limited to adults who are returning home in the community, because the investigators are primarily interested in the problems and unmet needs encountered after discharge during the recovery period at home.
To enhance the generalizability of the results, the sample will be stratified based on 2010 national estimates of age categories for hospitalized adults.
Description
Inclusion Criteria:
- 18 years or older
- Able to read and speak English
- Returning home in the community after discharge
Exclusion Criteria:
- Discharged to facility care
- Pregnant females
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
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
High ESDP Score
Patients with 10 or greater score on the Early Screen for Discharge Planning at the time of admission.
|
This screen is completed by a study coordinator within 24 hours of patient admission to the hospital.
The screen measures four variables available from routine hospital admission clinical data (walking limitation, age, living alone prior to admission, and level of disability) that exhibit high sensitivity and specificity (AUC's were .82
and.84) in identifying patients who should receive targeted attention from a DP expert.
|
Low ESDP Score
Patients with 9 or lower score on the Early Screen for Discharge Planning at the time of admission.
|
This screen is completed by a study coordinator within 24 hours of patient admission to the hospital.
The screen measures four variables available from routine hospital admission clinical data (walking limitation, age, living alone prior to admission, and level of disability) that exhibit high sensitivity and specificity (AUC's were .82
and.84) in identifying patients who should receive targeted attention from a DP expert.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of problems reported after discharge, measured by the Problems After Discharge Questionnaire - English Version (PADQ-E)
Time Frame: 1 week after hospital discharge
|
A problem is defined as any worry, limitation, concern, or difficulty reported by the patient.
The Problems After Discharge Questionnaire - English Version measures important patient factors often overlooked that contribute to poor post-acute recovery experience which are recognized as important factors likely to impact readmission.
|
1 week after hospital discharge
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of unmet needs reported after discharge, measured by the Problems After Discharge Questionnaire - English Version (PADQ-E)
Time Frame: 1 week after hospital discharge
|
An unmet need is a need for help identified by the patient that is reported to be inadequately met.
The Problems After Discharge Questionnaire - English Version measures important patient factors often overlooked that contribute to poor post-acute recovery experience which are recognized as important factors likely to impact readmission.
|
1 week after hospital discharge
|
Quality of life, measured by the EuroQoL-5D
Time Frame: 1 week after hospital discharge
|
The EuroQoL-5D (EQ-5D) is a standardized instrument for use as a measure of health out-come.
Applicable to a wide range of health conditions and treatments, it provides a simple descriptive profile and a single index value for health status that can be used in the clinical and economic evaluation of health care.
|
1 week after hospital discharge
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Diane E. Holland, PhD, RN, Mayo Clinic
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
June 1, 2014
Primary Completion (Actual)
May 1, 2015
Study Completion (Actual)
May 1, 2015
Study Registration Dates
First Submitted
April 16, 2014
First Submitted That Met QC Criteria
April 16, 2014
First Posted (Estimate)
April 21, 2014
Study Record Updates
Last Update Posted (Estimate)
May 21, 2015
Last Update Submitted That Met QC Criteria
May 20, 2015
Last Verified
May 1, 2015
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 14-002495
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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