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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01647243
Other study ID # M-20110181
Secondary ID
Status Recruiting
Phase N/A
First received July 13, 2012
Last updated July 20, 2012
Start date January 2012
Est. completion date December 2013

Study information

Verified date July 2012
Source University of Aarhus
Contact Birgit Sørensen Skoffer, MPH
Phone +45 50 42 28 30
Email BSkoffer@dadlnet.dk
Is FDA regulated No
Health authority Denmark: Danish Dataprotection Agency
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate if preoperative strength training will result in faster recovery and higher level of function six weeks after total knee arthroplasty (TKA).


Description:

Reduced strength of the quadriceps muscle is a common clinical finding in patients with Knee Osteoarthritis and this seems to play a central role in the development of the disease. The strength of the quadriceps muscle have been shown to be reduced by 20-40% as compared to age-matched healthy controls and this decrease in muscle strength have been closely associated with a reduced level of function and increase of pain. Furthermore, it has been demonstrated that the preoperative strength of the quadriceps muscle in patients undergoing TKA, is associated with the level of function one year after surgery. Compared to the level before the operation, an additional operation-induced reduction of the strength of the quadriceps muscle up to 60% as has been demonstrated. Presumably, an optimizing of the strength of the quadriceps muscle could counteract the impact of the expected postoperative loss of muscle strength to such an extent that the loss will be of less clinical significance. It is hypothesized that an optimizing of the strength of the quadriceps muscle may have a favorable effect on the postoperative rehabilitation program and shorten the period of convalescence.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date December 2013
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Planned TKA at the Aarhus University Hospital or Region Hospital Silkeborg,

- Living in Aarhus Municipality,

- Primary knee osteoarthritis or secondary osteoarthritis after meniscectomy or ligament injury

Exclusion Criteria:

- Unstable blood pressure,

- Neuromuscular or neurodegenerative disease,

- Comprehension or dementia problems

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Preoperative strength training
Progressive strength training on group basis (not more than 3 subjects) 3 sessions weekly starting 4 weeks before the operation, in total 12 sessions Strength training 3 sessions weekly 4 weeks postsurgery

Locations

Country Name City State
Denmark Aarhus University hospital Aarhus

Sponsors (1)

Lead Sponsor Collaborator
University of Aarhus

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Primary outcome: Sit-to-stand test Ability of function test Change from Baseline 6 weeks preoperative in Sit-to-Stand at 6 weeks postoperative No
Secondary Isokinetic: Quadriceps 60 gr./sek Muscle strength test in dynamometer 6 weeks and 1 week before the operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary Isokinetic: Hamstrings 60 gr./sek Muscle strength test in dynamometer 6 weeks and 1 week before the operation, 1 week, 6 weeks 12 weeks and 1 year after the operation No
Secondary Isometric: Quadriceps (70 gr. flexion) Muscle strength test in dynamometer 6 weeks and 1 week before the operation and 11 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary Isometric: Hamstrings (20 gr. flexion) Muscle strength test in dynamometer 6 weeks and 1 week before the operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary Rate of force development (flexion and extension) Muscle test in dynamometer 6 weeks and 1 week before the operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary Timed Up and Go Ability of function test 6 weeks and 1 week before the operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary 10 meter walk test Ability of function test 6 weeks and 1 week before the operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary 6 minute walk test Ability of function test 6 weeks and 1 week before operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary Knee injury and Osteoarthritis Outcome Score (KOOS) Disease-specific questionnaire 6 weeks and 1 week before operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary Oxford Knee Score (OKS) Disease-specific questionnaire 6 weeks before the operation and 6 weeks after No
Secondary EuroQol-5 dimensions (EQ-5D) Generic questionnaire for self-rated health 6 weeks and 1 week before the operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary Short-Form Health Survey (SF 12) Generic questionnaire for self-rated health 6 weeks before the operation and 1 year after No
Secondary Background data questionnaire Questionnaire about pain, medicine use, alcohol intake, smoking, education, job 6 weeks and 1 week before the operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary Range of motion of the knee Extension of the knee Flexion of the knee 6 weeks and 1 week before the operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
Secondary Body mass index Weight/height2 6 weeks and 1 week before the operation, 1 week, 6 weeks, 12 weeks and 1 year after the operation No
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