MedPath

Effects of aquatic training on knee cartilage

Completed
Conditions
Osteoarthritis
Musculoskeletal Diseases
Other arthrosis
Registration Number
ISRCTN65346593
Lead Sponsor
niversity of Jyväskylä (Finland)
Brief Summary

1. 2013 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/23497162 2. 2016 results in https://www.ncbi.nlm.nih.gov/pubmed/27211862 (added 21/01/2019) 3. 2017 results of the relationship between physical activity and cartilage quality in women with knee osteoarthritis, in https://www.ncbi.nlm.nih.gov/pubmed/28240703 (added 21/01/2019) 4. 2017 results of the effects of high-intensity resistance aquatic training on body composition and walking speed in women with mild knee osteoarthritis, in https://www.ncbi.nlm.nih.gov/pubmed/28263901 (added 21/01/2019)

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
80
Inclusion Criteria

1. Voluntary women 60-68 years of age, regular intensive exercise (such as strength training) no more than two times a week
2. No history of any illness for which exercise is contraindicated or that would limit their participation in the Aquatic exercise program
3. Subjects with mild to moderate knee pain during the last 12 months
4. Willingness and voluntarily signed informed consent to undergo testing and intervention procedures with all of its aspects
5. Weight-bearing knee x-rays show Kellgren-Lawrence grade 1-2 OA according to Altman et al.(1986)

Exclusion Criteria

1. Body-mass index over 34
2. Knee instability or trauma that would jeopardize the training
3. Inflammatory joint disease
4. Intra-articular steroid injections in the preceding 3 months in the knee

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<br> Cartilage measurements<br> Structural changes of the tibiofemoral and patella cartilage will be revealed by Magnetic Resonance Imaging (MRI) at 1.5T magnetic field strength. The combination of two techniques will be used, T2 relaxation time, indexing the collagen component of cartilage, and dGEMRIC, reflective of glycosaminoglycan concentration, volumetric MRI assessment of cartilage thickness and morphology. Also, the quality of subchondral bone will be evaluated. In our laboratory, the reproducibility of bulk dGEMRIC is good (CVrms 4.2 ?4.8%)<br><br> Body composition:<br> Dual energy X-ray absorptiometry (DXA) will be performed to assess body composition. The body fat, lean body mass as well as femoral neck and lumbar spine areal bone mineral density (BMD, g/cm2) and bone mineral content (BMC, g) will be analyzed.<br>
Secondary Outcome Measures
NameTimeMethod
<br> 1. Knee pain will be evaluated by a 100 mm visual analog scale (VAS)<br> 2. Physical function and clinically-important symptoms will be evaluated by Knee Injury and Osteoarthritis<br> 3. Knee Injury and Osteoarthritis Outcome Score (KOOS) and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)<br> 4. X-ray (weight-bearing anteroposterior and mediolateral radiographs) will be taken from both knees for the classification of osteoarthritis of the knee<br> 5. Quality of life will be evaluated by the RAND 36-Item Health Survey questionnaire<br> 6. Muscle strength (leg extension and flexion) will be measured using an adjustable dynamometer chair (Good Strength; Metitur, Jyväskylä, Finland)<br> 7. Muscle power will be measured with a Nottingham powerrig<br> 8. Dynamic balance and agility will be evaluated with a timed figure of 8 running test<br>
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