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Effectiveness and cost-effectiveness of a novel rehabilitation strategy in people undergoing primary total knee replacement surgery. The MARKER (Maximum Recovery After Knee Replacement Surgery) Study.

Recruiting
Conditions
Primary total knee replacement surgery for osteoarthritis
Musculoskeletal - Osteoarthritis
Registration Number
ACTRN12609000054213
Lead Sponsor
Dr Marlene Fransen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
600
Inclusion Criteria

undergoing unilateral or bilateral primary total knee replacement surgery, able to provide informed consent, able to be discharged home from the orthopaedic ward

Exclusion Criteria

(i) previous unicompartmental replacement or tibial osteotomy on the same knee, (ii) previous lower limb joint replacement surgery within the last six months, (iii) further lower limb joint replacement surgery anticipated within the next 12 months, (iv) major co-morbidity precluding aerobic exercise at 50-60% maximum heart rate, (v) rheumatoid arthritis, (vi) major neurological conditions, or (vii) inability to return to one of the participating sites for outpatient exercise classes

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain subscale on the Western Ontario and McMaster Universities (WOMAC) Scale (pain in the knee over the last 48 hours)[6 weeks, 6 months and 12 months after randomisation];Physical function subscale on the Western Ontario and McMaster Universities (WOMAC) Scale (difficulties in physical activities in the knee over the last 48 hours)[6 weeks, 6 months and 12 months after randomisation]
Secondary Outcome Measures
NameTimeMethod
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