Knee Osteoarthritis Clinical Trial
— PBFR3Official title:
Assessment of Efficacy of Low Intensity Resistance Training in Men at Risk for Symptomatic Knee Osteoarthritis
Verified date | January 2016 |
Source | University of Iowa |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The purpose of this research study is to determine whether low intensity resistance training
with concurrent application of a peripheral blood flow restriction device to the exercising
limb will elicit increased quadriceps strength, functional gains, ability to complete
knee-related activities of daily living, mobility, and quality of life in individuals at
risk for developing symptomatic knee osteoarthritis (OA). It is known that higher quadriceps
strength is protective against developing symptomatic knee OA.1 However, people at risk for
knee OA frequently do not tolerate the high intensity resistance training that is generally
believed necessary to increase muscle strength. Partial blood flow restriction (PBFR) to the
exercising muscle has been reported to result in strength gains, while requiring lower
levels of joint loading.2 This method may be better tolerated, enabling efficacious exercise
in older adults who may not tolerate high knee joint loads.
To asses the efficacy of a 4 week low-intensity resistance training program with concurrent
application of PBFR to the exercising limbs to improve quadriceps strength and size, leg
muscle power, and mobility in individuals at risk for developing symptomatic knee
osteoarthritis,we will test the following hypotheses. In comparison with low-intensity
resistance training without use of PBFR, a four-week low-intensity resistance-training
program with PBFR will:
Primary Hypothesis: Increase (a) double leg-press 1RM strength and (b) isokinetic knee
extensor strength
Secondary Hypotheses:
1. Increase quadriceps muscle volume assessed by MRI
2. Increase lower limb muscle power on (a) double leg-press at 40% 1RM and (b) a timed
stair climb
3. Not adversely effect knee pain or quality of life assessed by the Knee injury and
Osteoarthritis Outcome Score (KOOS) questionnaire
Status | Completed |
Enrollment | 44 |
Est. completion date | February 2012 |
Est. primary completion date | February 2012 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 45 Years and older |
Eligibility |
Inclusion Criteria: - male - = 45 years - has at least one of the following: BMI=25, frequent knee symptoms on most of the last 30 days, history of knee injury which rendered individual unable to walk without assistance for at least 2 days, history of knee surgery, diagnosis of knee osteoarthritis Exclusion Criteria: - Resistance training at any time in the last 3 months prior to study - Bilateral knee replacement - Lower limb amputation - Lower limb surgery in the last 6 months that affects walking ability or ability to exercise - Back, hip or knee problems that affect walking ability or ability to exercise - Unable to walk without a cane or walker - Inflammatory joint or muscle disease such as rheumatoid or psoriatic arthritis or polymyalgia rheumatica - Multiple sclerosis - Known neuropathy - Self-report of Diabetes - Currently being treated for cancer or having untreated cancer - Terminal illness (cannot be cured or adequately treated and there is a reasonable expectation of death in the near future) - Peripheral Vascular Disease - History of myocardial infarction or stroke in the last year - History of deep venous thrombosis - Chest pain during exercise or at rest - Use of supplemental oxygen - Inability to follow protocol (e.g. lack of ability to attend visits or understand instructions) - Staff concern for subject health (such as history of dizziness/faintness or current restrictions on activity) - Concurrent study participation - Unable to attend more than 2 days within any 1 week or unable to attend 4 or more sessions during the study |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor)
Country | Name | City | State |
---|---|---|---|
United States | University of Iowa | Iowa City | Iowa |
Lead Sponsor | Collaborator |
---|---|
University of Iowa |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Isotonic Leg Press 1RM | double leg press 1 rep maximum strength | 0,6 weeks | No |
Secondary | Isokinetic Knee Extensor Strength | 0, 6 weeks | No | |
Secondary | Knee Pain | Knee injury and Osteoarthritis Outcome Score (KOOS) questionnaire Pain Sub-Scale (0-100); larger absolute values represent less pain; a positive % changes indicates a reduction in pain | 0, 6 weeks | Yes |
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