- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05964972
Impact of an Automatic Alert Device on the Occurrence of Nocturnal Falls in Nursing Home Residents (NOCTUSAFE)
July 22, 2025 updated by: University Hospital, Caen
Impact of an automatic alert device on the occurrence of nocturnal falls in nursing home residents Measurement of the number of nocturnal falls between 8 p.m. and 8 a.m. per registered resident in the 6 months preceding use of the device compared with the number of nocturnal falls in the 6 months after installation of the device.
Study Overview
Status
Terminated
Conditions
Study Type
Observational
Enrollment (Actual)
8
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
-
-
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Cagny, France
- Ehpad Les Orchidees
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-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Fallers
Description
Inclusion Criteria:
- Resident of the elderly nursing home (EHPAD LES ORCHIDEES).
- Repeated nocturnal falls (more than 2 falls at night between 8 p.m. and 8 a.m.) during the last 12 months.
- Consent of the resident or his legal representative.
- Signature of informed consent
- French-speaking resident.
Exclusion Criteria:
- Refusal to participate in the study.
- Resident exclusive day faller.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
number of falls
Time Frame: 6 month preceding and 6 month after
|
Measurement of the number of nocturnal falls between 8 p.m. and 8 a.m. per registered resident in the 6 months preceding use of the device compared with the number of nocturnal falls in the 6 months after installation of the device.
|
6 month preceding and 6 month after
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
May 17, 2022
Primary Completion (Actual)
December 30, 2023
Study Completion (Actual)
December 30, 2024
Study Registration Dates
First Submitted
July 20, 2023
First Submitted That Met QC Criteria
July 20, 2023
First Posted (Actual)
July 28, 2023
Study Record Updates
Last Update Posted (Actual)
July 25, 2025
Last Update Submitted That Met QC Criteria
July 22, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 19-145
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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