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OpenTrials
Completed

NCT Number: NCT00163787

Clinical Identification of Fall Risk Early After Unilateral Transtibial Amputation

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.

Completed

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Austin Health Royal Talbot Rehabilitation Centre

Melbourne, Victoria, 3101, Australia

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • over 18 years unilateral transtibial amputee

Exclusion criteria

  • visually unable to perform tests cognitively unable to perform tests unable to provide informed consent not being discharged into supported accommodation

Treatment and study plan

outcome measures and self report

Behavioral

Sponsors and collaborators

Lead sponsor

Bayside Health

Other Gov

Collaborators

  • Austin Health

Registry information

Official study title

Clinical Identification of Increased Fall Risk Early After Unilateral Transtibial Amputation

Important dates

Study start
2003
Study completion
2005
First posted
Sep 14, 2005
Registry last updated
Oct 25, 2005

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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