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The effect of progressive resistance training on knee articular cartilage morphology in osteoarthritic patients

The effect of 6 month high intensity progressive resistance training on knee articular cartilage morphology in female osteoarthritic patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12605000116628
Acronym
REACH
Enrollment
60
Registered
2005-08-09
Start date
2005-04-02
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Subjects will be randomised into a progressive resistance training (PRT) or sham-exercise group. The PRT group will train at 80% of their peak strength, using Keiser pneumatic resistance machines, and progress approximately 3% per session. Strength will be re-assessed fortnightly. Exercises will target muscles around the hip and knee. The sham-exercise group will train on the same equipment as the PRT group except hip adduction, but without added resistance or progression. Both groups will train

Subjects will be randomised into a progressive resistance training (PRT) or sham-exercise group. The PRT group will train at 80% of their peak strength, using Keiser pneumatic resistance machines, and progress approximately 3% per session. Strength will be re-assessed fortnightly. Exercises will target muscles around the hip and knee. The sham-exercise group will train on the same equipment as the PRT group except hip adduction, but without added resistance or progression. Both groups will train 3 days per week for roughly 45 minutes for 6 months.

Sponsors

University of Sydney, Faculty of Health Sciences, School of Exercise and Sport Science
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Primary Osteoarthritis in at least one knee using standard criteria of the American College of Rheumatology (ACR) criteria for classification of clinical osteoarthritis -Ambulatory without human assistance-Willingness to be randomised to experiential or control group-Ability to attend scheduled exercise and testing sessions

Exclusion criteria

Regular exercise of any kind over the past 3 months (>1dpw). -Secondary osteoarthritis (traumatic or post-surgical), rheumatic disease, gouty or septic arthritis, Paget's disease, pseudogout, major congenital abnormalities, hemochromatosis, Wilson's disease and other rare forms of arthritis -Joint injury, injection or surgery within the past 6 months or knee joint replacement.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026