Skip to main content
Clinical Trials/ACTRN12612000501842
ACTRN12612000501842
Recruiting
未知

A randomised controlled trial of the effects of progressive resistance training, high protein/low glycaemic index diet and gait re-training on knee adductor moment in overweight/obese adults with medial knee osteoarthritis.

niversity of Sydney0 sites125 target enrollmentMay 9, 2012

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity of Sydney
Enrollment
125
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 9, 2012
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • The following inclusion criteria enable the volunteer to participate in the THE LO Study:
  • \- Primary osteoarthritis of at least one knee
  • \- BMI \>27\.5 kg/m2
  • \- Aged 40 years or more
  • Criteria used to make OA diagnosis:
  • \- Knee pain
  • \- \+ve at least 1 of 3:
  • \- Age \> 50 years
  • \- Stiffness \< 30 minutes
  • \- Crepitus

Exclusion Criteria

  • The following conditions permanently exclude the subject from participation in the THE LO STUDY:
  • \- Unstable aortic aneurysm
  • \- Rapidly progressive or terminal illness
  • \- Severe left ventricular dysfunction/end stage congestive heart failure
  • \- Severe aortic stenosis
  • \- Secondary osteoarthritis (traumatic or post\-surgical), rheumatic disease, gouty or septic arthritis, Paget's disease, pseudogout, major congenital abnormalities, hemachromatosis, Wilson's disease and other rare forms of arthritis)
  • \- Previous or anticipated (within 6\-12 months) joint replacement operation
  • \- Severe psychosis or behavioural disturbance or cognitive impairment
  • \- Surgery to any structure (cartilage, bone, tendons, ligaments, muscle) in or around the knee joint
  • The following conditions require medical intervention or re\-evaluation prior to participation in THE LO Study:

Outcomes

Primary Outcomes

Not specified

Similar Trials