Skip to main content
Clinical Trials/NCT02771834
NCT02771834
Completed
Not Applicable

Evaluation of the Association Between Osteoporosis and Postural Balance in Postmenopausal Women

University of Sao Paulo0 sites126 target enrollmentJuly 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postural Balance
Sponsor
University of Sao Paulo
Enrollment
126
Primary Endpoint
International Physical Activity Questionnaire
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The incidence of osteoporosis has been increasing, as have fractures resulting from falls.

Detailed Description

The overall objective of this study is to evaluate bipodal postural balance in postmenopausal women with and without lumbar osteoporosis. The specific objective is to determine the relationship between the degree of thoracic kyphosis and dosing of 25 OH vitamin D with postural balance in postmenopausal women with lumbar osteoporosis. One hundred and twenty-six postmenopausal women between 55-65 years of age were evaluated and separated into two groups according to the bone mineral density values of their lumbar spine: the osteoporosis group and the control group. Functional mobility was evaluated through the Timed Up and Go Test. Postural balance was evaluated using a AccuSway® model portable force platform, in standard standing position, with eyes open and closed, for 60". Data were collected, stored, and processed by the Balance Clinic® program, configured to 100 Hz frequency, with a frequency cut-off filter at 10 Hz. Muscle strength was evaluated via a Biodex® isokinetic dynamometer in the concentric/concentric knee extension mode at 60o/s. Dosing of 25 OH vitamin D and thoracic spine x-rays to determine the degree of kyphosis measured by the Cobb angle were performed in the osteoporosis group.

Registry
clinicaltrials.gov
Start Date
July 2009
End Date
December 2012
Last Updated
9 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Guilherme Carlos Brech

Phd

University of Sao Paulo

Eligibility Criteria

Inclusion Criteria

  • absence of impairment of the vestibular, proprioceptive, auditory or neurological system, and/or any mental disturbances or disorders;
  • no use of medications that might compromise postural balance;
  • absence of lesions, surgery or disease that might have caused lower-limb joint limitations over the previous six months;
  • absence of lower-limb dysmetria;
  • presence of clinically normal gait, without claudication.

Exclusion Criteria

  • the presence of pain or inability to complete any of the tests
  • along with occurrences of blood pressure increase before the strength evaluation.

Outcomes

Primary Outcomes

International Physical Activity Questionnaire

Time Frame: 1 day

Secondary Outcomes

  • Functional mobility(1 day)

Similar Trials