CREATION Health Readmission Risk Assessment Tool
| Status: | Recruiting |
|---|---|
| Conditions: | Chronic Obstructive Pulmonary Disease, Pneumonia, Cardiology, Cardiology, Neurology, Orthopedic, Orthopedic |
| Therapuetic Areas: | Cardiology / Vascular Diseases, Neurology, Pulmonary / Respiratory Diseases, Orthopedics / Podiatry |
| Healthy: | No |
| Age Range: | 21 - Any |
| Updated: | 3/30/2019 |
| Start Date: | May 15, 2017 |
| End Date: | January 2020 |
| Contact: | Jo Wheeler, RN |
| Email: | jo.wheeler@flhosp.org |
| Phone: | 407-609-9022 |
This study occurs in two phases. Phase 1 involves initial item development and measurement
validation of a new tool for identifying hospitalized patients at high risk for preventable
readmission. Primary tasks include item construction and content validation, data collection,
analysis, and instrument refinement. Phase 2 involves administering the refined instrument to
a new group of patients to determine final item content for the instrument, its factor
structure, and its predictive validity.
validation of a new tool for identifying hospitalized patients at high risk for preventable
readmission. Primary tasks include item construction and content validation, data collection,
analysis, and instrument refinement. Phase 2 involves administering the refined instrument to
a new group of patients to determine final item content for the instrument, its factor
structure, and its predictive validity.
Participants will complete the instrument on an electronic device provided by research staff
in the hospital room. If an individual is unable to complete the instrument, the participant
may have another individual input answers on the electronic device. Hospitalized patients (n
= 1240: 620 in Phase 1 and 620 in Phase 2) with a variety of chronic diseases will be
recruited into the study. Study coordinators will recruit participants with the following
diagnoses: heart failure, chronic obstructive pulmonary disease, acute myocardial infarction,
coronary artery bypass graft, pneumonia, total knee or hip replacement, and stroke. These
diagnoses were chosen because of the frequency with which patients are readmitted after
discharge.
in the hospital room. If an individual is unable to complete the instrument, the participant
may have another individual input answers on the electronic device. Hospitalized patients (n
= 1240: 620 in Phase 1 and 620 in Phase 2) with a variety of chronic diseases will be
recruited into the study. Study coordinators will recruit participants with the following
diagnoses: heart failure, chronic obstructive pulmonary disease, acute myocardial infarction,
coronary artery bypass graft, pneumonia, total knee or hip replacement, and stroke. These
diagnoses were chosen because of the frequency with which patients are readmitted after
discharge.
Inclusion Criteria:
- Primary or secondary admission diagnosis of heart failure, chronic obstructive
pulmonary disease, acute myocardial infarction, coronary artery bypass graft,
pneumonia, total knee or hip replacement, or stroke.
- Age 21 and over
- Able to provide informed consent
- Able to speak and read English
- Able to complete an electronic survey or relay answers to questions to another party
who may complete the survey for the participant
- Resides in Central Florida and anticipates continued residence in Central Florida for
the next 120 days
- Planned discharge to a non-hospital or residential care environment
Exclusion Criteria:
- Under age 21
- Does not speak or read English
- Permanent residence is outside Central Florida
- Not of cognitive capacity to provide valid responses
- Dementia or cognitive impairment that renders subject unable to provide informed
consent
- Prescribed a known psychoactive medication that might reasonably affect the ability of
the participant to provide valid responses
We found this trial at
1
site
601 E Rollins St
Orlando, Florida 32803
Orlando, Florida 32803
(407) 303-5600
Principal Investigator: Patricia Robinson
Phone: 407-609-9022
Florida Hospital Florida Hospital is one of the country
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