- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04365673
LACE+ and MRS Score Readmission Rate Assessment
March 2, 2022 updated by: Tabula Rasa HealthCare
Comparing the Predictive Strength of the LACE+ Index With the MedWise Rise Score on Hospital Readmission Rates: a Non-inferiority Observational Study
A study to demonstrate that the LACE+ score in non-inferior to the medication risk score when predicting 30-day readmission post hospital discharge.
Study Overview
Status
Terminated
Conditions
Intervention / Treatment
Detailed Description
The objective of this study is evaluate a program that provides transition of care services to a local Tucson hospital involving activities designed to reduce 30 day post hospital discharge readmission rates.
The organization has had a fee for service contract with this hospital since 2017 to provide pharmacist delivered transition of care services.
The organization collects internal tracking outcome data as part of the contract deliverable and is required to report it to the hospital once per month.
The investigators look to assess LACE+ and medication risk scores to learn if there is an association with the 30 day post hospital discharge readmission rate post pharmacist intervention.
The outcomes will not be generalizable and will be reported back to the hospital client to demonstrate value added.
Study Type
Observational
Enrollment (Actual)
100
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
-
-
Arizona
-
Tucson, Arizona, United States, 85701
- Tabula Rasa HealthCare
-
-
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 to 88 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Information will be collected from an internal data collection excel used to provide monthly outcome intervention reports to the local Tucson hospital.
Description
Inclusion Criteria:
- Those referred to receive transition of care services between January 2018 to December 2019 and were discharged on 10 or more medications.
Exclusion Criteria:
- 89 years or older
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: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Readmitted
Patients that were readmitted within 30 days post hospital discharge
|
Pharmacist-delivered comprehensive medication review
|
|
Not readmitted
Patients that were not readmitted within 30 days post hospital discharge
|
Pharmacist-delivered comprehensive medication review
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Readmission
Time Frame: 2018 - 2019
|
Readmission within 30-days post hospital discharge
|
2018 - 2019
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jennifer Bingham, PharmD, Tabula Rasa HealthCare
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 (Actual)
July 7, 2020
Primary Completion (Actual)
March 1, 2021
Study Completion (Actual)
March 1, 2021
Study Registration Dates
First Submitted
April 24, 2020
First Submitted That Met QC Criteria
April 24, 2020
First Posted (Actual)
April 28, 2020
Study Record Updates
Last Update Posted (Actual)
March 17, 2022
Last Update Submitted That Met QC Criteria
March 2, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- TRHC_RD_LACEMRS_2020
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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