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Clinical Trials Stage of 'SoleSensor': A Balance-Enhancing Shoe Insert.
This study has been completed.
First Received: September 6, 2005   No Changes Posted
Sponsors and Collaborators: Wilfrid Laurier University
Sunnybrook Health Sciences Centre
Information provided by: Wilfrid Laurier University
ClinicalTrials.gov Identifier: NCT00151359
  Purpose

Our research has shown that pressure sensation from the soles of the feet (plantar mechanoreceptors) plays an important role in controlling several key aspects of balancing reactions, particularly during compensatory stepping . As a result, age-related loss of plantar pressure sensation, which is very common, can lead to impaired control of these reactions. However, we have shown that it is possible to compensate for balance impairments resulting from this loss of sensation by using special footwear insoles to facilitate sensation from the perimeter of the sole. To date, we have demonstrated the feasibility of this approach in laboratory studies, and we have obtained a U.S. patent for the design concept. However, it remains to be determined whether the benefits of the footwear persist over the long term, or whether there is a habituation of the effect. Also, we need to determine whether there are any practical problems associated with wearing such footwear, e.g. due to discomfort or irritation of the skin.


Condition Intervention
Sensation Disorder
Device: SoleSensor

Study Type: Observational
Study Design: Longitudinal, Defined Population, Prospective Study
Official Title: Clinical Trials Stage of 'SoleSensor': A Balance-Enhancing Shoe Insert.

Further study details as provided by Wilfrid Laurier University:

Study Start Date: February 2002
  Eligibility

Ages Eligible for Study:   65 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Aged 65 to 75 years

Exclusion Criteria:

  • Any neurological or musculoskeletal ailments that affect their balance
  • Any drugs that affect balance
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00151359

Locations
Canada, Ontario
WLU Biomechanics Laboratory
Waterloo, Ontario, Canada, N2L 3C5
Sponsors and Collaborators
Wilfrid Laurier University
Sunnybrook Health Sciences Centre
Investigators
Principal Investigator: Stephen D Perry, PhD Wilfrid Laurier University
Principal Investigator: Brian E Maki, PhD Centre for Studies In Aging, Sunnybrook & Women's
Principal Investigator: Geoff R Fernie, PhD Centre for Studies In Aging, Sunnybrook & Women's
  More Information

Publications:
Study ID Numbers: PPP-53686
Study First Received: September 6, 2005
Last Updated: September 6, 2005
ClinicalTrials.gov Identifier: NCT00151359     History of Changes
Health Authority: Canada: Ethics Review Committee

Study placed in the following topic categories:
Signs and Symptoms
Sensation Disorders
Neurologic Manifestations

Additional relevant MeSH terms:
Signs and Symptoms
Sensation Disorders
Nervous System Diseases
Neurologic Manifestations

ClinicalTrials.gov processed this record on August 30, 2009