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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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10 December 2012 |
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Main ID: |
NCT01345825 |
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Date of registration:
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29/04/2011 |
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Primary sponsor: |
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Public title:
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Early Progressive Strength Training to Patients With Unicompartmental Knee Replacement
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Scientific title:
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A Randomized Controlled Trial: The Effectiveness of 8-weeks Progressive Strength Training to Patients With Unicompartmental Knee Replacement, Initiated Within the First Postoperative Week |
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Date of first enrolment:
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March 2011 |
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Target sample size:
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60 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01345825 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
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Countries of recruitment
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Denmark
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Contacts
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Name:
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Søren Bie Bogh |
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Address:
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Telephone:
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Email:
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sorenbiebogh@gmail.com |
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Affiliation:
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Name:
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Søren Bie Bogh |
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Address:
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Telephone:
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+45 42343553 |
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Email:
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sorenbiebogh@gmail.com |
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Affiliation:
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Name:
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Kjeld Søballe |
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Address:
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Telephone:
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Email:
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Affiliation:
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Orthopaedic Surgery Research Unit, Aarhus |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- medial osteoarthrosis in knee assigned to unicompartmental knee replacement
- 18+ years.
Exclusion Criteria:
- rheumatoid arthritis
- neuro muscular conditions
- alcohol or drug abuse
- cognitive problems
- patients not fluid in the Danish language
- walking disability caused by other than in condition in question
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Knee Osteoarthritis
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Intervention(s)
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Other: Resistance training
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Primary Outcome(s)
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Muscle power test (by a power rig)
[Time Frame: prior to operation (baseline), 9 weeks post operativ and 1 year post operative]
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Secondary Outcome(s)
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Gait quality
[Time Frame: prior to operation (baseline), 9 weeks post operativ and 1 year post operative]
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Secondary ID(s)
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M-20100185
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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