Actively Recruiting

Early Phase 1
Age: 50Years - 95Years
All Genders
NCT06906939

A Randomized Pilot rTMS Trial for Knee Arthritis Pain and Depression

Led by University of California, Los Angeles · Updated on 2026-03-13

30

Participants Needed

1

Research Sites

169 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Osteoarthritis (OA) is a major public health problem, and involvement of the knee is especially disabling. Symptomatic knee OA has an incidence rate between 40 to 1,020 per 100,000 person years1 and is among the most common causes of disability worldwide. Knee arthritis pain and disability are highly comorbid wiht depression (30-50%). Currently available treatments offer only limited relief. The Pilot project aims to establish feasibility of the rTMS neuromodulation of response to Tai Chi and improvement in pain and comorbid depression in patients with knee OA. There are several ways in which the pilot project will improve scientific knowledge, and clinical practice: 1) The sequential stimulation of two targets (M1 and l-DLPFC) has not been systematically examined for the treatment of comorbid MDD and knee OA. We hypothesize that using a multi-target rTMS strategy combining M1 and l-DLPFC- active targets will be well tolerated and more effective to treat comorbid symptoms than single site rTMS to M1+l-DLPFCsham. This hypothesis will be tested in Aim 1 of this proposal by comparing two experimental conditions: A) M1active and l-DLPFCactive; and B) M1active and l-DLPFCsham. 2) Identifying the relationship between improvement in pain and depression to improvement in pro-inflammatory cytokines would be novel. Adding an rTMS as a neuromodulation technique with novel stimulation sites to assist in the reduction of symptoms of pain and depression is another scalable to clinical use opportunity that will provide pilot data for future clinical trials. We will perform a pilot feasibility trial of rTMS for those presenting with knee osteoarthritis related pain and moderate to severe depression in 30 volunteers who are undergoing Tai Chi intervention. Tolerability and safety of rTMS added to Tai Chi will be assessed along with changes in symptoms of pain and depression, in preparation to future R-01 applications.

CONDITIONS

Official Title

A Randomized Pilot rTMS Trial for Knee Arthritis Pain and Depression

Who Can Participate

Age: 50Years - 95Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 50 years or older
  • Chronic pain of 6 months or more in one or more body regions
  • Meet American College of Rheumatology criteria for symptomatic knee osteoarthritis with radiographic evidence or have knee pain for 3 months or more on most days in the past month
  • PROMIS Pain Interference score of 40 or higher
  • Access to a computer or device for telehealth
  • Able to walk without cane or assistance
  • Persistent depressive symptoms with Beck Depression Inventory score over 20 on two screenings within 2-3 weeks
  • Willingness to complete the 3-month study including twice-weekly Tai Chi and rTMS, plus 6- and 12-month follow-ups
  • Approval to participate from primary care provider or medical team member
  • Ability to pass the Physical Activity Readiness Questionnaire (PAR-Q) via phone screening
  • No contraindications to rTMS
Not Eligible

You will not qualify if you...

  • Change in psychotropic or pain medication in the past 4 months
  • Current diagnosis of mania, hypomania, unstable bipolar disorder, psychotic disorder, or history of psychosis
  • Dementia, neurological disease, cancer, cardiovascular, metabolic, renal, liver disease, or other serious medical conditions limiting participation in Tai Chi or exercise
  • Medical conditions preventing safe participation in moderate exercise
  • Alcohol or drug dependence within the past 3 months
  • Currently practicing Tai Chi

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UCLA Semel Institute - Neuropsychiatric Institute (NPI)

Los Angeles, California, United States, 90095

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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