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Comparison of post-discharge physiotherapy versus usual care following total knee replacement: a randomised clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN07624314
Enrollment
107
Registered
2004-09-30
Start date
2003-08-20
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

Surgery: post-operative care Surgery Post-operative care

Interventions

Current interventions as of 02/07/2008: The intervention group patients received two physiotherapy home visits. The first visit took place within two weeks of discharge and the second visit was 6 - 8

Sponsors

Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Added as of 02/07/2008: Age range and gender was unspecified; all patients undergoing an elective primary total knee arthroplasty for osteoarthritis and who reside within the community of Oxfordshire were eligible.

Exclusion criteria

Exclusion criteria: Added as of 02/07/2008: 1. Patients undergoing bilateral arthroplasty 2. Minimally invasive surgery and metal-to-metal implants 3. Patients where further joint surgery is planned within the next twelve months 4. Patients with inflammatory arthritis 5. Patients whose existing co-morbities prevent them from participating in the proposed treatment intervention 6. Patients who are unable to provide informed consent

Design outcomes

Primary

MeasureTime frame
Current primary outcome measures as of 02/07/2008: Oxford Knee Score. Trial patients underwent reassessment, using all outcome measures, at three and twelve months post-operatively by a physiotherapist blind to trial arm allocation. Patients were also followed up at six months post-operatively by postal questionnaire containing Oxford Knee score, the Knee injury and Osteoarthritis Outcome Score (KOOS) and the EuroQol. Previous primary outcome measures: Changes in Oxford Hip and Knee and Iowa Level of Assistance Scores, timed sit-to-stand, EuroQol and resource use diaries.

Secondary

MeasureTime frame
Added as of 02/07/2008: 1. The Knee injury and Osteoarthritis Outcome Score (KOOS) 2. The timed sit-to-stand test 3. The timed walk test 4. The Leg extensor press 5. Joint range of motion 6. The EuroQol questionnaire (EQ-5D) 7. Patient diaries to collect heath resource utilisation Trial patients underwent reassessment, using all outcome measures, at three and twelve months post-operatively by a physiotherapist blind to trial arm allocation. Patients were also followed up at six months post-operatively by postal questionnaire containing Oxford Knee score, the Knee injury and Osteoarthritis Outcome Score (KOOS) and the EuroQol.

Countries

United Kingdom

Outcome results

None listed

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