Status:

COMPLETED

Study of the Relationship Between the Strength of Ankle Movement Muscles and Postural Parameters in Elderly Fallers: Towards New Strategies for Screening and Management

Lead Sponsor:

Centre Hospitalier Universitaire Dijon

Conditions:

Persons Who Have Experienced a Sudden Uncontrolled Fall in the Absence of Outside Factors in the 6 Months Preceding the Consultation

Eligibility:

All Genders

60-90 years

Brief Summary

The quality of life of elderly citizens is to a great extent related to the maintenance of independence. The risk of falling and the loss of autonomy are two frequent problems associated with ageing. ...

Eligibility Criteria

Inclusion

  • Control group:
  • Subjects who have provided written informed consent
  • Subjects with national health insurance cover
  • Subjects aged between 60 and 90 years old
  • Able to understand simple instructions and exercise instructions and to provide informed consent
  • with no diseases that could compromise postural abilities and ankle muscle strength.
  • Subjects who have not experience a sudden uncontrolled fall in the absence of outside factors in the 6 months preceding inclusion.
  • Patients group
  • Subjects who have provided written informed consent
  • Subjects with national health insurance cover
  • Subjects aged between 60 and 90 years old
  • Able to understand simple instructions and exercise instructions and to provide informed consent
  • Subjects who have experienced at least one sudden uncontrolled fall in the absence of outside factors in the 6 months preceding inclusion.

Exclusion

  • Acute balance disorders (central vestibular syndrome, infection or toxic cause)
  • Chronic vestibular disease with proven clinical repercussions
  • Any severe neuro-orthopedic disease impairing balance as well as physiological impairments due to ageing Any chronic neurological disorder (stroke, Parkinson syndrome…)
  • Any psychiatric disorder able to compromise participation
  • Non-corrected vision disorder
  • Cancer or any progressive disease
  • Treatment with psychotropic agents able to impair vigilance and posture
  • Patients under guardianship
  • Patients with an ADL score \<3 (total of 6 points), reflecting a clinically obvious high risk of falling

Key Trial Info

Start Date :

March 1 2011

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

December 1 2016

Estimated Enrollment :

34 Patients enrolled

Trial Details

Trial ID

NCT03343769

Start Date

March 1 2011

End Date

December 1 2016

Last Update

November 17 2017

Active Locations (1)

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CHU Dijon Bourgogne

Dijon, France, 21000