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Clinical Trials/NCT03678402
NCT03678402
Completed
N/A

Testing the Effectiveness of a Falls Prevention System

Tammy Moore1 site in 1 country521 target enrollmentJune 24, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
High Risk for Falling
Sponsor
Tammy Moore
Enrollment
521
Locations
1
Primary Endpoint
High Risk Fall Rate
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this single arm intervention study is to determine if the fall rate (as measured by falls per 1000 patient days) for patients designated "high fall risk" decreases with the use of the PUP™ [Patient is UP Falls Prevention System] when compared to the historical falls rate data for the prior 12 months from those same nursing units within the OSUWM Brain & Spine Hospital.

Detailed Description

The purpose of this single arm intervention study is to determine if the fall rate (as measured by falls per 1000 patient days) for patients designated "high fall risk" decreases with the use of the PUP™ \[Patient is UP Falls Prevention System\] when compared to the historical falls rate data for the prior 12 months from those same nursing units within the OSUWM Brain \& Spine Hospital. All Brain and Spine Hospital patients will be evaluated as to fall risk using the current fall risk assessment tool employed by OSU Medical Center and administered in the usual and customary fashion upon evaluation on the floor and Pod. Patients who are determined to be at a high fall risk will be approached to participate. Those patients who consent to participate in the study will remain in the study until a nurse removes the patient from high risk fall status or the participant has been discharged from the hospital. Any patient fall will to be reported and evaluated following current processes and procedures developed by the OSU Brain and Spine Institute as maintained with IHIS; the PUP™ as the intervention for this study will be an adjunct to those fall prevention processes already in place.

Registry
clinicaltrials.gov
Start Date
June 24, 2019
End Date
June 30, 2020
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Tammy Moore
Responsible Party
Sponsor Investigator
Principal Investigator

Tammy Moore

Director of Nursing, Neurological Institute

Ohio State University

Eligibility Criteria

Inclusion Criteria

  • Age 18 years of age or older;
  • All high-risk fall patients, eighteen years of age or older, who are admitted to the OSU Brain and Spine Hospital on Floors 8 South, 9 South, 10 South, 8 East, 9 East or 10 East. Patients will undergo a pre-assessment as per OSUWMC procedure to determine if they are a high-fall risk.

Exclusion Criteria

  • Patients whose medical condition as assessed by the PI prohibits their participation in the program, which would include among others the following: patients who lack the capacity to consent, patients with an anatomy or wound issue on their feet or around their calves that would bar them from wearing socks on either foot, and/or patients for whom the sock would impede medical treatment.

Outcomes

Primary Outcomes

High Risk Fall Rate

Time Frame: hospital stay (on average 5 days)

To determine if the fall rate (as measured by falls per 1000 patient days) for patients designated "high fall risk" decreases with the use of the intervention (Patient is UP fall prevention technology \[PUP™ \]) when compared to historical NDNQI data for the prior 12 months ("Benchmark Data") from nursing units where the intervention is being undertaken.

Study Sites (1)

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