Assessment of an Automated Telesurveillance System on Serious Falls Prevention in an Elderly Suffering From Dementia Specialized Care Unit: the URCC
NCT ID: NCT01561872
Last Updated: 2015-02-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
350 participants
OBSERVATIONAL
2012-04-30
2015-02-28
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Assessment of an Automated Telesurveillance System on the Incidence of Serious Falls in Nursing Homes
NCT01551121
Home-Based Technologies Coupled to Teleassistance Service in the Elderly
NCT01697553
Superiority of Intelligent Video Surveillance + Telealarm Over Telealarm Alone in Elderly People at Risk of Falling
NCT05875038
Assessment of Teleconsulting in Nursing Homes
NCT02157740
Telemonitoring of Activities of Daily Living in Home Care Services of Older Adults with Cognitive Deficits
NCT06888713
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
intervention group
Rooms of the patient of the "intervention group" will be equipped of cameras
No interventions assigned to this group
reference group
Patient in the "non-equipped" group will have usual care
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patient admitted in Limoges or Brive's URCC
* Patient informed consent and/or proxy consent
* Patient covered by the French health insurance
Exclusion Criteria
* Patient with a short term prognosis pathology
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Limoges
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Thierry DANTOINE, MD
Role: STUDY_DIRECTOR
University Hospital, Limoges
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Limoges University Hospital
Limoges, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
I11 005
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.