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Effective Rehabilitation of Patients Operated With Total Knee Arthroplasty

Effective Rehabilitation of Patients Operated With Total Knee Arthroplasty

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01877733
Enrollment
41
Registered
2013-06-14
Start date
2013-01-31
Completion date
2015-07-31
Last updated
2020-04-22

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

Conditions

Osteoarthritis

Keywords

Resistance training

Brief summary

The purpose of this study is to investigate the effect of maximal strength training (MST) compared to standard rehabilitation in patients operated with total knee arthroplasty. Previous studies report reduced physical function and muscle strength despite successful surgery inserting an artificial implant. Furthermore, great loss of muscle strength has been found in these patients in the early postoperative phase. The study is a randomized controlled trial. The investigators hypothesize that MST will increase muscle strength and physical function more than standard rehabilitation.

Interventions

Sponsors

St. Olavs Hospital
CollaboratorOTHER
Helse Nord-Trøndelag HF
CollaboratorOTHER
Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* unilateral osteoarthritis, * \< 75 years

Exclusion criteria

* disease(s) that compromise testing/training, * unable to understand written and verbal instructions and information, * osteoarthritis in the contralateral leg that needs treatment.

Design outcomes

Primary

MeasureTime frameDescription
Muscle strength in leg extension and leg pressMeasured preoperatively, after 7 days, 10 wks and 1 yearMeasured preoperatively implies measuring the outcome within the last month prior to surgery

Secondary

MeasureTime frameDescription
EQ-5D (measure of health outcome)Preoperatively (within 1 month prior to surgery), 7 days, 10 wks and 1 year postoperatively
VAS scale recording painpreoperatively (within 1 month prior to surgery), 7 days, 10 wks and 1 year postoperatively
6 minute walk testpreopertively, 7 days postoperatively and after 1 yearMeasuring the outcome preoperatively implies testing within the last month prior to surgery
KOOS; Knee injury and osteosarthritis outcome scorePreoperatively (within 1 month prior to surgery), 7 days postoperatively and 10 wks and 1 year postoperatively

Countries

Norway

Outcome results

None listed

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