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CompletedNCT01561872GET-BETTERUpdated Feb 13, 2015

Assessment of an Automated Telesurveillance System on Serious Falls Prevention in an Elderly Suffering From Dementia Specialized Care Unit: the URCC

An observational study in Mentally Ill Old Subjects, sponsored by University Hospital, Limoges. Completed at 1 site in France. Open to participants aged 65 Years and older. Per ClinicalTrials.gov, last updated 2015-02-13.

Sponsored by University Hospital, Limoges · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
350
Ages
65 Years and older
Sex
All
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Study summary

2 URCC in the Limousin region will be equipped with the automated telesurveillance system. Patient will be selected by ward's geriatrician and randomized into two groups after informed consent. One group will have cameras installed and the other will not and will act as a comparison group. Patient will be assessed twice during the study, at admission in (inclusion visit) and at outcome from the URCC (end of study visit). Each assessment implies a standard geriatric assessment, a fall questionnaire, a Neuropsychiatric inventory for behavioral disturbances and a quality of life questionnaire (EQ5D). Every fall will be considered as adverse events and will therefore be listed along the study and characterized in types and number.

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Conditions studied

  • Mentally Ill Old Subjects

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03

In context

Dementia

2,172 studies on the registry are indexed under Dementia; 540 are open to participants now.

This study's enrollment of 350 is above the median of 250 across 482 observational studies indexed under Dementia.

Browse Dementia studies →

Lead sponsor

University Hospital, Limoges is the lead sponsor of 255 studies on the registry; 36 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

demented old subjects

Inclusion criteria

  • Patient aged more than 65 years old
  • Patient admitted in Limoges or Brive's URCC
  • Patient informed consent and/or proxy consent
  • Patient covered by the French health insurance

Exclusion criteria

Exclusion Criteria:

  • Patient without national health insurance coverage
  • Patient with a short term prognosis pathology
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
350 participants (actual)

Groups and cohorts

  • intervention group

    Rooms of the patient of the "intervention group" will be equipped of cameras

  • reference group

    Patient in the "non-equipped" group will have usual care

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What researchers measure

Primary outcomes

  1. The impact of the automated telesurveillance system

    The impact of the automated telesurveillance system on the incidence rate of falls with serious outcomes between the two groups during their hospitalization in URCC.

    Time frame: 6 months

Secondary outcomes

  1. The impact of the system on the global rate of falls

    Time frame: 6 months

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Study locations

1 site
  • Limoges University Hospital
    Limoges, 87042, France
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 13, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01561872
Lead sponsor
University Hospital, Limoges
Responsible party
Sponsor
First posted
Mar 23, 2012
Start date
Apr 2012
Primary completion
Nov 2014
Completion
Feb 2015
Last update
Feb 13, 2015

Study contacts

Thierry DANTOINE, MD
study director · University Hospital, Limoges

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2015. You cannot join it, but the record below documents what was studied.

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