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Behavioural Intervention
Exercise for Chronic Knee Pain
N/A
Recruiting
Research Sponsored by University of Texas, El Paso
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Knee pain at least 4 on a 0-10 pain scale
Age ≥45
Must not have
Inability to perform exercise due to severe pain or other symptoms
Peripheral neuropathy or other sensation loss on the body sites for pain measurements (i.e., the wrist, knee, the forearm)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 1: ts will be assessed twice. ts assessment --> 25 minutes of waiting --> ts assessment; time frame of days 2 and 3 will be the same except 25 minutes of waiting time. it will be 25 minutes of exercise (either ae or le) on days 2 and 3
Awards & highlights
No Placebo-Only Group
Summary
This trial studies the effects of arm and leg exercise on knee pain in people with knee osteoarthritis. It also explores how race, income, and stress affect the effectiveness of exercise.
Who is the study for?
This trial is for people over 45 with knee osteoarthritis and a pain level of at least 4 out of 10. They must understand English, have activity-related knee pain, and not have morning stiffness lasting over half an hour. Excluded are those with pacemakers, pregnant women, severe diseases, past knee replacements, sensation loss where pain is measured, chronic opioid use or certain arthritis types.
What is being tested?
The study tests how arm exercises using an arm ergometer versus leg exercises on a cycling ergometer affect pain relief after exercise in individuals with knee osteoarthritis. It also examines the impact of socioeconomic factors and stress on this exercise-induced hypoalgesia through a pilot randomized cross-over design.
What are the potential side effects?
While specific side effects aren't listed for these exercises, participants may experience general discomfort or muscle soreness typical to new physical activities. The risk of injury exists if exercises are performed improperly.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My knee pain is at least a 4 out of 10.
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I am 45 years old or older.
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I experience knee pain when I move.
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I don't have morning joint stiffness, or it lasts 30 minutes or less.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I cannot exercise because of severe pain or symptoms.
Select...
I have numbness or loss of feeling in areas like my wrist, knee, or forearm.
Select...
I do not have rheumatoid arthritis, ankylosing spondylitis, or neurological disorders that would interfere with the study.
Select...
I do not have any serious uncontrolled health conditions.
Select...
I have had knee replacement surgery.
Select...
I have difficulty with memory or thinking clearly.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ day 1: ts will be assessed twice. ts assessment --> 25 minutes of waiting --> ts assessment; time frame of days 2 and 3 will be the same except 25 minutes of waiting time. it will be 25 minutes of exercise (either ae or le) on days 2 and 3
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 1: ts will be assessed twice. ts assessment --> 25 minutes of waiting --> ts assessment; time frame of days 2 and 3 will be the same except 25 minutes of waiting time. it will be 25 minutes of exercise (either ae or le) on days 2 and 3
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Changes in pressure pain thresholds (Measure of exercise-induced hypoalgesia)
Conditioned pain modulation
Knee pain
+1 moreSecondary study objectives
Acculturative Stress
Autonomic function
Emotional support
+8 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: ExerciseExperimental Treatment1 Intervention
Arm 1: All participants, knee OA and pain-free individuals, will undergo a single exercise of arm exercise using an arm ergometer and;
Group II: Lower Body ExerciseActive Control1 Intervention
Arm 2: All participants, knee OA and pain-free individuals, will undergo a single exercise of leg exercise using a cycling ergometer.
Find a Location
Who is running the clinical trial?
University of Texas, El PasoLead Sponsor
15 Previous Clinical Trials
2,899 Total Patients Enrolled
1 Trials studying Osteoarthritis
30 Patients Enrolled for Osteoarthritis
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