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Sponsors and Collaborators: |
Bayside Health Austin Health |
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Information provided by: | Bayside Health |
ClinicalTrials.gov Identifier: | NCT00163787 |
All participants attend for two testing sessions at either Royal Talbot Rehabilitation Centre or the centre where they received inpatient physiotherapy services. All participants will be tested at discharge and at six months post discharge. Personnel used to score and administer the balance tests at six months will be blinded to pre-test scores, subject background, as well as, mobility and fall history in the six months post discharge.
At discharge participants will perform two successful Four Square Step Tests (FSST, and will be videotaped performing the Timed Up and Go Test (TUGT. The turn measure will be scored from this TUGT. Participants will also complete the Locomotor Capabilities index (LCI). At the six-month test participants repeat balance and mobility tests and LCI, as well as being interviewed to ascertain fall history since discharge.
Condition | Intervention |
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Amputation |
Behavioral: outcome measures and self report |
Study Type: | Observational |
Study Design: | Natural History, Longitudinal, Convenience Sample, Retrospective/Prospective Study |
Official Title: | Clinical Identification of Increased Fall Risk Early After Unilateral Transtibial Amputation |
Estimated Enrollment: | 50 |
Study Start Date: | June 2003 |
Estimated Study Completion Date: | August 2005 |
Subjects:
All unilateral trans-tibial amputees with prosthesis at discharge, who are over 18 years of age, willing to participate and give informed consent. Subjects will be excluded if visually unable to perform tests, cognitively unable to follow testing procedures or being discharged into supported accommodation.
Identify scores for unilateral trans-tibial amputees for; FSST, TUGT and turn measure items: (1) steps, (2) time and (3) steadiness & fluency of movement. Evaluate the validity, predictive value, sensitivity & specificity of the balance and mobility measures for falls and community ambulation with trans-tibial amputees.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Australia, Victoria | |
Austin Health Royal Talbot Rehabilitation Centre | |
Melbourne, Victoria, Australia, 3101 |
Principal Investigator: | Wayne Mr Dite, MAppSci | Austin Health Royal Talbot Rehabilitation Centre |
Study ID Numbers: | 79/03 |
Study First Received: | September 12, 2005 |
Last Updated: | October 24, 2005 |
ClinicalTrials.gov Identifier: | NCT00163787 History of Changes |
Health Authority: | Australia: National Health and Medical Research Council |
mobility falls activity level |