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Behavioural Intervention

Remote Tai Chi for Knee Osteoarthritis (TAICHIKNEE Trial)

N/A
Waitlist Available
Led By Robert Saper, MD, MPH
Research Sponsored by Tufts Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age 50 years or older
Treating clinician diagnosis of knee osteoarthritis
Must not have
Unable to walk without a cane or other assistive device
Any previous reconstructive surgery
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months from randomization
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to see if doing Tai Chi online can help reduce knee pain in adults with knee osteoarthritis. They want to know if doing Tai Chi can make it easier to do physical,

Who is the study for?
This trial is for adults with knee osteoarthritis who experience pain that affects their daily activities. Participants will be randomly assigned to either add remote Tai Chi sessions to their routine care or continue with their usual treatment without Tai Chi.
What is being tested?
The study is testing if practicing Tai Chi remotely can reduce the impact of knee pain on physical, mental, and social activities. It also looks at improvements in knee function and whether participants use fewer painkillers as a result.
What are the potential side effects?
Tai Chi is generally considered low-risk; however, some may experience mild discomfort or muscle soreness when starting any new exercise regimen.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 50 years old or older.
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My doctor diagnosed me with knee osteoarthritis.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I need a cane or another device to walk.
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I have had reconstructive surgery before.
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I do not speak English.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months from randomization
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months from randomization for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Secondary study objectives
Number of knee joint injections
Other study objectives
Beck Depression Inventory-II score
OMERACT/OARSI responder
PROMIS Pain Interference score
+10 more

Awards & 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: Tai Chi + Routine CareExperimental Treatment1 Intervention
The intervention will be delivered via a HIPAA-secure web-based video platform. All remote Tai Chi sessions will be 60 minutes, twice a week, for 3 months. All program components will use the Yang style Tai Chi, and every session will include warm up, review of principles, meditation with movement, breathing techniques and relaxation.
Group II: Routine CareActive Control1 Intervention
Participants will be encouraged to continue their ongoing care for Knee OA by their providers. In addition, primary care providers and other participating clinicians in the health system will receive information from the study team on routine care or "2019 ACR Guideline-Based Care." At the end of the 12-month trial period, routine care participants will be offered access to recordings for the full 3-month Tai Chi program (24 sessions).

Find a Location

Who is running the clinical trial?

University of California, Los AngelesOTHER
1,561 Previous Clinical Trials
10,258,526 Total Patients Enrolled
3 Trials studying Osteoarthritis
132 Patients Enrolled for Osteoarthritis
Tufts Medical CenterLead Sponsor
263 Previous Clinical Trials
263,988 Total Patients Enrolled
9 Trials studying Osteoarthritis
763 Patients Enrolled for Osteoarthritis
Boston Medical CenterOTHER
401 Previous Clinical Trials
883,349 Total Patients Enrolled
1 Trials studying Osteoarthritis
138 Patients Enrolled for Osteoarthritis
~320 spots leftby Dec 2026