Clinical Trials Directory

Trials / Completed

CompletedNCT02117804

Early Screen for Discharge Planning in Community Hospitals

Validating Discharge Planning Decision Support in a Regional Community Hospital

Status
Completed
Phase
Study type
Observational
Enrollment
225 (actual)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

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.

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.

Conditions

Interventions

TypeNameDescription
OTHEREarly Screen for Discharge PlanningThis 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.

Timeline

Start date
2014-06-01
Primary completion
2015-05-01
Completion
2015-05-01
First posted
2014-04-21
Last updated
2015-05-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02117804. Inclusion in this directory is not an endorsement.