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A Targeted Strengthening Program Following Total Hip Replacement.

U

University of Melbourne

Status

Completed

Conditions

Total Hip Joint Replacement

Treatments

Behavioral: Strength training program

Study type

Interventional

Funder types

Other

Identifiers

NCT00222300
H2002/01532

Details and patient eligibility

About

Total Hip Replacement (THR) is a common surgical procedure performed in people with hip osteoarthritis and appears to be effective in relieving pain and improving function. However significant wasting and weakness of the hip and knee muscles persists post-operatively. Although relief of pain and improvement of function are important outcomes following THR, weakness of the hip and knee muscles reduces a person's ability to manage stairs, slopes, public transport and results in persistent gait abnormalities. Since lower limb weakness is one of the risk factors for falls, it is important that patients undergo a strengthening program post-operatively. The hypothesis is that lower limb strength and function will be better in patients who undergo a strengthening program post-operatively than in those who have usual care.

Full description

Total Hip Replacement (THR) is a common surgical procedure performed in people with hip osteoarthritis and appears to be effective in relieving pain and improving function. However significant quadriceps atrophy and weakness persist post-operatively. Although relief of pain and improvement of function are important outcomes following THR, weakness of the hip and knee muscles reduces a person's ability to manage stairs, slopes, public transport and results in persistent gait abnormalities. Since lower limb weakness is one of the risk factors for falls, it is important that this is appropriately addressed.

The study examines the effect of an eight-week task-specific strengthening program on lower limb function in patients following THR in a randomized controlled trial. The experimental program is being conducted as a circuit in a gymnasium environment. Changes on specific measures of physical function of patients in the Experimental Group will be compared with those of patients in a Control Group who will continue with the standard care program provided at Austin Health.

Outcome measures include:lower limb muscle strength using a step test, pain, stiffness, and function as reported on the WOMAC questionnaire, quality of life using the AQoL questionnaire, the Timed Up-and-Go test. Walking tests will also be conducted. These include:

  1. Walking pattern, recorded on an instrumented mat
  2. Walking endurance measured by the 6-minute walk test.
  3. Analysis of hip joint torques using 3-D motion analysis.

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • primary uncomplicated total hip joint replacement 6-8 weeks prior to enrolment.
  • able to walk 45m independently with or without walking aid.
  • able to comprehend instructions
  • prior joint replacement on the other side at least 12 months previously

Exclusion criteria

  • unable to fully weight-bear on affected limb
  • pre-existing neurological or orthopaedic condition affecting gait
  • revision surgery
  • post-operative complications, e.g. wound infection
  • uncontrolled systemic disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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