- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05224765
Reducing G60 Recidivism Rates
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Risk of future falls in elderly patients increases based on multiple factors including increased age and history of previous falls. However, there is limited research showing evidenced-based interventions that reduce recidivism rates related to falls. The Centers for Disease Control and Prevention (CDC) has an evidenced-based fall prevention program (Stopping Elderly Accidents, Deaths & Injuries [STEADI3]). Implementation of STEADI as part of a multidisciplinary approach to fall risk assessment and prevention prior to discharge may reduce recidivism in elderly patients.
Ground level falls are the most common mechanism of injury in older adults and are increasingly becoming a significant cause of morbidity and mortality in this population. An individual's risk of a repeat ground level fall increases after an initial fall, injury, or hospitalization7. Addressing fall risk factors and tailoring inpatient care for any trauma in the elderly population prior to discharge will likely improve outcomes, decrease length of stay, and decrease morbidity and mortality.
The introduction of STEADI as part of a specialized multidisciplinary approach to fall risk assessment and prevention prior to hospital discharge may reduce recidivism in elderly patients. Patients that attend the discharge class are typically more likely to go home and return to independence whereas those that do not attend the discharge class are likely to have a disposition of going to a long-term care facility or are not mentally capable of retaining information. Reduced falls as a result of STEADI implementation will putatively improve mortality rates and quality of life in elderly patients.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
Texas
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Dallas, Texas, United States, 75203
- Methodist Dallas Medical Center
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 60 years or older
- G60 activation and admission
- Primary admission for injury
Exclusion Criteria:
- Less than 60 years old
- Admitted for non-traumatic injuries
- Non-index admission for injury
- Prisoners
- Pregnant or lactating subjects
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Geriatric patients that attended fall prevention discharge class
recidivism rates of MDMC-qualified G60 patients that attended fall prevention discharge class per hospital protocols
|
Participants attend fall prevention discharge class per hospital protocols
|
|
Geriatric patients that did not attend fall prevention discharge class
recidivism rates of MDMC-qualified G60 patients that did not attended fall prevention discharge class per hospital protocols
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of patients with repeat Emergency Department(ED) visits with a chief complaint associated with a fall.
Time Frame: 2019-2022
|
review of G60 patients across all MHS hospitals after system standard order set initiation and utilization as the comparative group for a 2-year period.
|
2019-2022
|
|
• Number of return visits related to a fall treated at a Methodist Health System(MHS)trauma center before and after implementation of G60 targeted education.
Time Frame: 2019-2022
|
• Observational study comparing recidivism rates of MDMC-qualified G60 patients that attended fall prevention discharge class per hospital protocols versus G60 patients that did not attend the class
|
2019-2022
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sarah Bradley, RN, Methodist Health System
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 036.TRA.2021.A
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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