Fall From Bed Clinical Trial
Official title:
A Phase One Feasibility Study of the Sensable®Care System: Establishing a Communications System for Patient Fall Reduction
Verified date | March 2019 |
Source | MedicusTek USA Corporation |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to test the effectiveness, safety and side effects of
Sensable®Care System for inpatients. The Sensable®Care System uses pressure sensors and
computer software to sense how patients are positioned on the bed in order to reduce bed
falls. The Sensable®Care System Mattress has sensors embedded in them, which will be
monitored by the nurses in your unit.
This study has three specific aims:
1. To assess the comfort of the system when used with hospitalized patients;
2. To observe how the system can be integrated into nurses' and hospital staff's regular
workflow to help to modify and improve the system.
3. To analyze data from nursing response to alerts generated from hospitalized patients to
improve alert system performance.
Status | Completed |
Enrollment | 71 |
Est. completion date | December 7, 2017 |
Est. primary completion date | October 21, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Gender: male or female - Age: 18 years and older - Racial and ethnic origin: all ethnic groups - Hospital status: admitted in-patient or a patient under observation - Expected hospital length of stay: minimum of 23 hours - Willingness to participate in the study - Moderate to High fall risk scoring a 2 or greater on the Mobility or Mental/LOC/Awareness status sections of the Hester Davis Fall Risk Assessment. Exclusion Criteria: - Declined to participate - Patients less than 18 years old - Patients who have been identified as a low fall risk or moderate fall risk with score less than 2 on the Mobility or Mental/ LOC/Awareness status sections of the Hester Davis Fall Risk Assessment - Women who are documented as pregnant during the study period - Patients who are medically unstable; as per the discretion of the primary nurse - Patients who are actively in the dying process, at the discretion of the primary nurse |
Country | Name | City | State |
---|---|---|---|
United States | Downey Medical Center | Downey | California |
Lead Sponsor | Collaborator |
---|---|
MedicusTek USA Corporation | Kaiser Permanente |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | % of Nursing Staff Who Want to Use the System Following the Trial | Acceptance of SensableCare System after Trial Period | focus group at week 8 within the 13 week study period | |
Primary | % of Nursing Staff Who Want to Use the System Following the Trial | Acceptance of SensableCare System after Trial Period | focus group at week 12 within the 13 week study period | |
Secondary | Rate of Bed Falls Decreased Over Study Period | Whether bed falls had decreased over the study period compared to before the start of the trial | through the 13 week study period |
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT03116386 -
Time Spent on Floor After Falls of Frailty People Overnight
|
N/A |