Knee Osteoarthritis Clinical Trial
Official title:
Determining Efficacy of the Combined Application of Electrical Stimulated Antagonist Contraction During Walking With Sensory TENS for Increasing Strength and Decreasing Pain in Women With Frequent Knee Symptoms
Verified date | June 2018 |
Source | University of Kansas Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Osteoarthritis of the knee (KOA) is the most common cause of disability in older adults.
Osteoarthritis involves a loss of cartilage, which acts like a cushion between the bones as
well as changes in the bones of joints. Once the joint cartilage is gone, the body does not
produce new cartilage. Joint damage can contribute to pain. Currently, treatment for pain
associated with knee osteoarthritis includes exercise. However, exercise at a medium- to
high-intensity level can be problematic for people with knee pain. Because exercise is a
common treatment for knee pain but many people experience pain during exercise, researchers
hope to find a safer and more effective exercise method to strengthen the muscles around the
knee.
Both aerobic exercise and resistance exercise are recommended for the treatment of people
with knee pain. However, pain can be a barrier to participating in exercise at a moderate or
vigorous intensity. Electrical stimulation of muscles holds potential to allow effective
exercise to be completed at tolerable intensities. Transcutaneous electrical nerve
stimulation (TENS) is the use of very low electric currents produced by a device to stimulate
the nerves, to treat pain. Neuromuscular electrical stimulation (NMES) uses low electrical
current to cause muscles to contract.
By doing this study, the investigators hope to learn if a hybrid training system (HTS), using
a combination of NMES and walking, is effective in strengthening muscles in people with knee
pain, aching or stiffness.
In this pilot study, the investigators will use walking with TENS as conventional exercise.
Randomized controlled trial will be conducted to compare the effect of walking augmented by
HTS with walking without HTS. The investigators will evaluate the relative advantages of
training that combines HTS with conventional walking exercise on the improvement of muscle
strength, physical function, and pain relief in obese women with frequent knee symptoms.
Study Hypotheses: Compared with walking with sensory TENS, walking with HTS will:
- 1 increase quadriceps muscle strength.
- 2 decrease knee pain.
Exploratory Hypotheses:
- 3 improve physical function.
- 4 increase PPT (improve central sensitization).
- 5 improve self-reported quality of life.
Status | Completed |
Enrollment | 28 |
Est. completion date | January 20, 2017 |
Est. primary completion date | January 20, 2017 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 39 Years to 70 Years |
Eligibility |
Inclusion Criteria: 1. Female 2. Age 40-70 years 3. Knee symptoms (pain, aching, or stiffness) on most of the last 30 days (categorically defined) 4. Body Mass Index (BMI) 30-45kg/m2 Exclusion Criteria: 1. Resistance training at any time in the last 3 months prior to the study 2. Bilateral knee replacement 3. Lower limb amputation 4. Lower limb surgery in the last 6 months that affects walking ability or ability to exercise 5. Back or hip problems that affect walking ability or ability to exercise 6. Unable to walk without a cane or walker 7. Inflammatory joint or muscle disease such as rheumatoid or psoriatic arthritis or polymyalgia rheumatica 8. Multiple sclerosis or other neurodegenerative disorder 9. Known neuropathy 10. Currently being treated with insulin for diabetes 11. Currently being treated for cancer or having untreated cancer 12. Terminal illness (cannot be cured or adequately treated and there is a reasonable expectation of death in the near future) 13. Peripheral Vascular Disease 14. History of myocardial infarction or stroke in the last year 15. Chest pain during exercise or at rest 16. Use of supplemental oxygen 17. Inability to follow protocol (e.g. lack of ability to attend visits or understand instructions) 18. Staff concern for participant health (such as history of dizziness/faintness or current restrictions on activity) 19. Unable to attend more than 2 days within any 1 week or unable to attend 4 or more sessions during the study 20. Implanted cardiac pacemaker, spinal cord stimulator, baclofen or morphine pump or other implanted electrical device. 21. Dermatitis or skin sensitivity to tape used in the study. 22. Pregnancy |
Country | Name | City | State |
---|---|---|---|
United States | University of Kansas Medical Center | Kansas City | Kansas |
Lead Sponsor | Collaborator |
---|---|
University of Kansas Medical Center | Kurume University |
United States,
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* Note: There are 29 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Knee Extensor Strength Assessed by Isokinetic Dynamometer. | Participants will be familiarized with strength testing equipment and counseled on proper lifting technique. They will undergo testing to determine their peak isokinetic knee extensor torque, using an isokinetic dynamometer. | Baseline and 12-week follow-up | |
Secondary | Change in Knee Flexor Strength Assessed by Isokinetic Dynamometer | Participants will be familiarized with strength testing equipment and counseled on proper lifting technique. They will undergo testing to determine their peak isokinetic knee flexor torque, using an isokinetic dynamometer. | Baseline and 12-week follow-up | |
Secondary | Change in Knee Pain Assessed by a Visual Analog Scale (VAS) | Knee pain will be evaluated using a visual analog scale (VAS) of 100 mm from no pain (0 mm) to the worst imaginable pain (100 mm). Participants will be asked to record their pain levels of the past one week. | Baseline and 12-week follow-up | |
Secondary | Change in Knee Pain Assessed by Knee Injury and Osteoarthritis Outcome Score (KOOS) | The Knee Injury and Osteoarthritis Outcome Score (KOOS) Pain subscale was used at baseline and follow-up to assess participant outcomes. The pain subscale is made up of 9 questions and was scored from zero to 100, with zero corresponding to extreme knee problems and 100 corresponding to no knee problems. | Baseline and 12-week follow-up | |
Secondary | Change in Quality of Life (QOL) Assessed by Knee Injury and Osteoarthritis Outcome Score (KOOS) | The Knee Injury and Osteoarthritis Outcome Score (KOOS) Quality of Life (QOL) subscale was used at baseline and follow-up to assess participant outcomes. The QOL subscale is made up of 4 questions and was scored from zero to 100, with zero corresponding to extreme knee problems and 100 corresponding to no knee problems. | Baseline and 12-week follow-up | |
Secondary | Change in 20-meter Walk Time. | Average time of two trials used for each participant. | Baseline and 12-week follow-up | |
Secondary | Change in 5-chair Stand Time. | Average time of two trials used for each participant. | Baseline and 12-week follow-up | |
Secondary | Change in Stair Climb Time. | Average time of two trials used for each participant. | Baseline and 12-week follow-up |
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