Skip to main content
Clinical Trials/NCT01545986
NCT01545986
Completed
N/A

A Comparative Analysis of High Velocity and Standard Low Velocity Exercise Training on Rehabilitation Outcomes Following Total Knee Arthroplasty

Helen Hayes Hospital1 site in 1 country38 target enrollmentSeptember 2009

Overview

Phase
N/A
Intervention
Not specified
Conditions
Osteoarthritis, Knee
Sponsor
Helen Hayes Hospital
Enrollment
38
Locations
1
Primary Endpoint
Change from Baseline in Six Minute Walk Test (6MWT) at six weeks
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study was to compare the effects of two exercise programs, using low velocity (LV) and high velocity (HV) contractions, on outcomes of individuals who have undergone total knee arthroplasty (TKA). The experimental hypothesis was that individuals performing HV exercise, compared to LV, would exhibit superior outcomes.

Detailed Description

The most effective type of exercise has not been identified for individuals who undergo total knee arthroplasty (TKA). High velocity (HV) exercise when compared to low velocity (LV) exercise produces greater gains in power and certain functional activities in older adults. The use of HV exercise for patients who undergo TKA has not been investigated.

Registry
clinicaltrials.gov
Start Date
September 2009
End Date
December 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marie A. Kardys Kelly

Primary Investigator

Helen Hayes Hospital

Eligibility Criteria

Inclusion Criteria

  • Adults aged 60- 89 years of age.
  • primary unilateral TKA 10-21 days prior to the outpatient PT evaluation
  • received inpatient rehabilitation at Helen Hayes Hospital

Exclusion Criteria

  • Any other lower extremity joint or back pain (not inclusive of recent Total knee arthroplasty) rated greater than four out of ten with weight-bearing
  • any other lower extremity joint replacement surgery
  • diagnosis of osteoporosis with history of fractures, uncontrolled hypertension, unstable cardiac or pulmonary problems, neurological disease affecting motor control, uncontrolled diabetes
  • chest pain or shortness of breath on stair-climbing
  • requirement of human assistance to walk in addition to the ambulation device
  • inability to follow instructions to perform testing and/or exercise,
  • participants who stated that they would not be available to complete 12 exercise sessions
  • individual adherence with performance of a home exercise program (HEP) less than five of seven days at the end of the treatment period

Outcomes

Primary Outcomes

Change from Baseline in Six Minute Walk Test (6MWT) at six weeks

Time Frame: 6 weeks

The distance walked in six minutes is measured for the 6MWT. A 150 foot hallway is used for the test. Standardized instructions are read to the participant. The participant is asked to walk as fast as he/she feels comfortable and safe in order to walk far as he/she can during six minutes. Distance is recorded in feet and later is converted to meters.

Secondary Outcomes

  • Gait Abnormality Rating Scale (GARS)(6 weeks)
  • Change from Baseline in Visual Analogue Scale (VAS) Pain at six weeks(6 weeks)
  • Change from Baseline in Timed Up and Go Test (TUG) at six weeks(6 weeks)
  • Gait Velocity(6 weeks)
  • Change from Baseline in Short Form-36 (SF-36) at six weeks(6 weeks)
  • Change from Baseline in Stair Climb Test at six weeks(6 weeks)

Study Sites (1)

Loading locations...

Similar Trials