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Pre-operative Rehabilitation Exercise Program for Total Knee Arthroplasty

Impact of a Pre-operative Rehabilitation Exercise Program for Patients With Severe Dysfunction Awaiting Total Knee Arthroplasty

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00493142
Acronym
PREP
Enrollment
240
Registered
2007-06-28
Start date
2008-07-31
Completion date
2021-11-25
Last updated
2022-07-15

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

Conditions

Osteoarthritis, Rheumatoid Arthritis

Brief summary

The purpose of this study is to determine whether a pre-operative home rehabilitation exercise program designed for knee replacements is more effective than pre-operative usual care.

Detailed description

Patients with lower levels of function prior to total knee arthroplasty (TKA) attain lower functional endpoints after surgery. Therapeutic exercise improves function in patients with arthritis of the knee, yet little evidence has examined the impact of pre-operative exercise for TKA. Single blinded randomized clinical trial comparing a pre-operative home exercise program to pre-operative usual care for patients who are waiting for TKA.Comparison group is usual care within the health region which does not include pre-operative rehabilitation program. Primary outcome: WOMAC function subscale. Secondary outcomes: 1) quality of life; 2) ambulation; 3) self-efficacy; 4) anxiety; 5) patient satisfaction; 6) cost-effectiveness of this intervention. Total Enrollment: 230 patients If the intervention improves function prior to surgery, results will be clinically applicable for patients waiting for surgery

Interventions

OTHERExercise
OTHERUsual care

Sponsors

Alberta Heritage Foundation for Medical Research
CollaboratorOTHER
Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
University of Alberta
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* primary unilateral total knee arthroplasty * poor functional status (WOMAC=50 or greater) * 50 yrs or older * reside within health region * understands English

Exclusion criteria

* unicompartmental total knee arthroplasty * revision surgery

Design outcomes

Primary

MeasureTime frameDescription
Self-reported function5 evaluations within 6 months after surgerySelf-reported function

Secondary

MeasureTime frameDescription
Quality of life, self-efficacy, ambulation, anxiety and patient satisfaction5 evaluations within 6 months after surgeryQuality of life
self-efficacy5 evaluations within 6 months after surgeryself-efficacy
ambulation, anxiety and patient satisfaction5 evaluations within 6 months after surgeryambulation
anxiety5 evaluations within 6 months after surgeryanxiety
patient satisfaction5 evaluations within 6 months after surgerypatient satisfaction

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026