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Pain Informed Movement for Knee Osteoarthritis
N/A
Recruiting
Led By Lisa Carlesso, PhD
Research Sponsored by McMaster University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
No Placebo-Only Group
Summary
This trial will compare two interventions for knee osteoarthritis to see if there are differences in pain, functional leg strength, pain modulation, and psychological factors.
Who is the study for?
This trial is for people over 40 with knee osteoarthritis who've had regular pain in the past month. They must speak English, have internet access, and be able to move without help. It's not for those with recent knee trauma/surgery, injections in the knee within 3 months, or involved in other OA trials.
What is being tested?
The study compares a pain informed movement program plus Pain Neuroscience Education (PNE) against standard neuromuscular exercises with basic OA education. It checks which is more feasible and satisfactory for patients and measures effects on pain, function, quality of life, strength, nerve factors.
What are the potential side effects?
While specific side effects are not listed here as it's an exercise-based intervention rather than drug-related; general risks may include muscle soreness or strain from physical activities.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Percentage of follow up
Secondary study objectives
Frequency of the program measured on a 5 point Likert scale
Rate of recruitment measured by number of people recruited in a year
Usefulness of the education content measured on a 5 point Likert scale
+5 moreOther study objectives
30 Second Sit to Stand Test
Brief Fear of Movement Scale for Osteoarthritis (BFMSO)
Conditioned Pain modulation (CPM) measured with PPT test stimulus and conditioning stimulus of forearm ischemia
+16 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: Pain Informed Movement and pain neuroscience educationExperimental Treatment2 Interventions
Participants will receive a twice weekly, 8 week in-person group exercise program, consisting of exercise instruction (75 minutes) and pain neuroscience education (PNE) videos (20 to 30 minutes/week for the first 4 weeks). During the exercise sessions, the educational components and concepts such as mindfulness, muscle tension regulation, and breathing techniques will be applied by the instructor. A third home session (weekly) will be facilitated by exercise handout sheets. The exercise component will be delivered by an experienced yoga teacher that has been extensively trained. The PNE video component will cover the following topics: The purpose of pain, neurophysiological changes of pain, movement guidelines when pain persists, and self-care techniques to impact neurophysiology and support moving with ease that include breath awareness and regulation, muscle tension regulation, awareness of pain related thoughts and emotions, relaxation, and body awareness.
Group II: Standard neuromuscular exercise and OA educationActive Control2 Interventions
Participants in this group will receive an 8-week in-person group exercise program held twice weekly, in which they will receive exercise instructions (60 minutes) and standard osteoarthritis (OA) education (15 to 20 minutes/week for the first 4 weeks). A third home session (weekly) will be facilitated by exercise handout sheets. The exercise component (i.e., the specific movements) of this group will be similar to those of the other group without the added techniques of breath awareness and regulation, muscle tension regulation, awareness of pain related thoughts and emotions, relaxation, and body awareness. The standard OA education videos will cover the following topics: common OA symptoms, risk factors associated with knee OA, and the effects of exercise and self-management tips. The exercise and education components will be delivered by a physiotherapist in the research team.
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Who is running the clinical trial?
Boston UniversityOTHER
470 Previous Clinical Trials
9,987,736 Total Patients Enrolled
12 Trials studying Osteoarthritis
5,940 Patients Enrolled for Osteoarthritis
University of British ColumbiaOTHER
1,465 Previous Clinical Trials
2,485,431 Total Patients Enrolled
26 Trials studying Osteoarthritis
1,912 Patients Enrolled for Osteoarthritis
University of MelbourneOTHER
181 Previous Clinical Trials
1,282,177 Total Patients Enrolled
13 Trials studying Osteoarthritis
703,285 Patients Enrolled for Osteoarthritis
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have had an injury or surgery on your legs in the last 6 months.You are currently receiving treatment for knee osteoarthritis pain from a healthcare provider like a physiotherapist, chiropractor, athletic therapist, or kinesiologist.You experience mild to moderate pain most days, with an average intensity of 3 out of 10 on a pain scale.You use devices like wheelchairs or walkers to help you move around.You have a condition like arthritis or other systemic issues that cause inflammation in your body.You have already taken part in a knee osteoarthritis exercise program within the last 3 months.You are at least 45 years old and have knee pain that gets worse with activity, even if it's just in the morning and lasts for about 30 minutes.
Research Study Groups:
This trial has the following groups:- Group 1: Standard neuromuscular exercise and OA education
- Group 2: Pain Informed Movement and pain neuroscience education
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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