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Risk Factors for Falls and Fall-related Injuries Associated With Mild Neurocognitive Disorders

Active, not recruiting
Conditions
Old Age
Fall Injury
Neurocognitive Disorders
Registration Number
NCT03978650
Lead Sponsor
Jewish General Hospital
Brief Summary

This study evaluates the risk for incident falls and fall-related injuries at the onset of neurocognitive disorders in older adults participating in the Canadian Longitudinal Study

Detailed Description

Falls are frequent events in adults over age 65 (up to 30% each year in Canada). They are a major Canadian public health concern, which negatively impacts health and quality of life of fallers, and health care system. Neurocognitive disorders are strongly associated with falls and fall-related injuries.

Several clinical characteristics, identified previously as risk factors for falls in the older population and in older adults with neurocognitive disorders are selected in the Canadian Longitudinal Study On Aging. The performance criteria of different statistical models will be compared for the association of neurocognitive disorders with falls and fall-related injuries. Six linear statistical models (i.e., logistic regression, discriminant analysis, Bayes network algorithm, decision tree, random forest, boosted trees), Factor Mixture Models and two different artificial neural network (i.e., multilayer perceptron and the neuroevolution of augmenting topologies).

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
12000
Inclusion Criteria
  • People who are 65 years and over
  • Men and women who live in Canada
Exclusion Criteria
  • People who do not live in Canada
  • A fall resulting from acute medical event and/or an external factor
  • Moderate to severe dementia

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fall Injury18 months

Incident falls occurring during the 18 months. Information related fall- injuries will also be collected, including fractures, dislocations, voluminous intracranial or peripheral hematomas, trauma of the face, and cutaneous lacerations of significant size and/or deeper than the hypodermis, possibly resulting in medical consultation or hospitalization.

Secondary Outcome Measures
NameTimeMethod
The Mental Alteration Testaround 20 years

Investigator will evaluate the amnesia

Auditory verbal memory disorderaround 20 years

Investigator will use the Rey Auditory Verbal Test that evaluates the auditory-verbal memory.

Trial Locations

Locations (1)

Jewish General Hospital

🇨🇦

Montréal, Quebec, Canada

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