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Multidisciplinary rehabilitation after primary total knee arthroplasty

Multidisciplinary rehabilitation after primary total knee arthroplasty: a randomised, controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN74292386
Enrollment
144
Registered
2008-06-30
Start date
2002-01-23
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Rehabilitation after primary total knee arthroplasty in knee osteoarthritis patients Musculoskeletal Diseases Gonarthrosis

Interventions

Patient information was provided according to the Declaration of Helsinki. The patients were first informed about the study by letter and then contacted by telephone by the head investigator or by the
simple mobility exercises for the lower limbs
maintenance of cardiovascular fitness) were recommended to all the participants by a physiotherapist when the decision of surgery was made. An outpatient control visit to an orthopedic surgeon was mad

Sponsors

Oulu University Hospital (Finland)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients scheduled for primary unilateral TKA in the Department of Surgery at the Oulu University Hospital were recruited from the surgical waiting list. The inclusion criteria were: 1. Diagnosis of primary OA of the knee 2. Both males and females, 60 - 80 years of age 3. Primary unilateral TKA as a scheduled procedure 4. Voluntary participation in the study

Exclusion criteria

Exclusion criteria: 1. Severe cardiovascular or pulmonary disease (New York Heart Association [NYHA] III - IV) 2. Severe dementia (Mini-Mental State Examination [MMSE] less than 18) 3. Rheumatoid arthritis 4. Primary TKA scheduled as a treatment of an acute trauma of the knee 5. Planned use of a special endoprosthesis

Design outcomes

Primary

MeasureTime frame
Self-reported functional ability and pain, assessed with the arthritis-specific Western Ontario McMaster Universities Osteoarthritis Index (WOMAC) composite score and subscale scores of pain, stiffness and function in both groups preoperatively and at the 2, 6 and 12-month follow-ups.

Secondary

MeasureTime frame
The following were assessed preoperatively and at 2-, 6- and 12-month follow-up: 1. HRQoL was measured with the generic 15D and the Rand 36-Item Health Survey 1.0 (Rand-36) 2. Demographic characteristics and surgical backgrounds were obtained preoperatively 3. Utilisation of rehabilitation services, assessed by a self-administered questionnaire at 2, 6 and 12 months after TKA 4. Physical performance tests: 4.1. Physical performance, objectively measured with a 15 metre (15 m) walk test and a stair test 4.2. Isometric strength of the knee was measured with the Lido Active Multijoint Rehabilitation System (Loredan Biomedical, USA) 4.3. Active knee flexion range of motion (ROM), measured with a standard long-arm goniometer Note: The physical performance tests were administered by five experienced physical therapists and two exercise physiologists, all of whom adhered to the protocol that included patient positioning, patient instructions, and evaluation of the results. The order of the tests remained constant throughout the study.

Countries

Finland

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026