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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03455894
Other study ID # 2016_58
Secondary ID 2017-A01910-53
Status Terminated
Phase N/A
First received
Last updated
Start date May 23, 2018
Est. completion date November 19, 2018

Study information

Verified date November 2018
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

DETECT'CHUTE CLINIBED is a smart carpet equipped with several sensors. Positioned at the foot of the bed, this system allows detecting i) patient fall out of the bed and ii) when patient is not back to bed after a certain time. When one of these two events is detected, the system then sends a short message syteme (SMS) and/or an email to the medical staff. The aim of this clinical study is to test the system ability to detect and transmit alarms for both those events.

In this clinical trial, the investigators will therefore test the alarms positive and negative predictive values for both the events.


Recruitment information / eligibility

Status Terminated
Enrollment 4
Est. completion date November 19, 2018
Est. primary completion date November 19, 2018
Accepts healthy volunteers No
Gender All
Age group 70 Years and older
Eligibility Inclusion Criteria:

- residents of the facility free to get up at night (without a barrier)

- residents may or may not be suffering from Alzheimer's disease or related illness.

- having fallen several times in the last 12 months and / or at risk of falling (time up and go test = 20 seconds).

Exclusion Criteria:

- Subject under tutelage

- use of night barriers or other forms of physical restraint deemed necessary by the physician in charge of the unit care or the patient

- Refusal of the resident's relatives.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
DETECT'CHUTE CLINIBED
The DETECT'CHUTE carpets will be positioned at night at the foot of the bed and set in motion by the nursing staff as soon as the elderly person goes to bed for the night. They will be withdrawn the next morning after the resident's rise. Each patient will benefit from the mat for 1 month.

Locations

Country Name City State
France CHU Lille

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary the positive predictive value of alerts Evaluation of the positive predictive value of alerts issued by the system. In the event of an alert, caregivers will immediately move to the resident's room to see if the alert has signaled a real fall or no return. During 30 days
Secondary the negative predictive value of alerts Measure the negative predictive value of fall and fall alerts. During 30 days
Secondary Time limit of the intervention of nurse After each alarm reception (fall or return) the intervention time will be estimated.
Regular rounds made by caregivers at the usual rhythm, and will see the appearance of a fall not signaled by the carpet.
During 30 days
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