Tai Chi for joint pain relief in women on aromatase inhibitors
Official title: Evaluating Tai Chi for Reducing Aromatase Inhibitor-Induced Arthralgia in Breast Cancer Survivors
Run by Thomas Jefferson University · NCT07737951 · Data updated 2026-11-12
This pilot study tests whether a Tai Chi program called TaiChi4Joint can help reduce AI-induced arthralgia in postmenopausal women with hormone receptor-positive breast cancer.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 40 (estimated) |
| Sponsor | Thomas Jefferson University Academic / other |
| Locations | 1 site (Philadelphia, Pennsylvania) |
| Status | Recruiting |
| Started | July 27, 2026 |
| Main results expected | June 2027 |
| Study ends | June 2029 |
| Registry record updated | August 14, 2026 |
| Trial ID | NCT07737951 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are postmenopausal women with stage I-III HR-positive breast cancer on AI therapy who have moderate joint pain and are willing to participate in virtual sessions.
✕Probably not a fit
Patients with pain not driven by AI therapy or who cannot participate in virtual sessions may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This nonrandomized pilot randomized trial compares TaiChi4Joint, a virtual Tai Chi program, with a health education attention control in women with stage I-III hormone receptor-positive breast cancer who are on an aromatase inhibitor and experience joint pain. Participants are randomized 1:1 to 12 weeks of online Tai Chi classes or health education, with assessments at baseline, after the program, and 2 months later. The study aims to assess feasibility and acceptability and to pilot data collection for biome behavioral mechanism measures. Eligible participants are postmenopausal adults on AI therapy within 5 years of initiation, reporting moderate joint pain, and able to complete procedures in English.
Why it matters
Potential benefit: If successful, participants may experience reduced AI-related joint pain and improved function.
How similar studies have gone: Prior studies in mind-body therapies for cancer-related symptoms have shown potential improvements, but this exact Tai Chi approach for AI-induced arthralgia is exploratory.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: -Individuals must meet all the following inclusion criteria in order to be eligible to participate in the study: * Age ≥18 years * Diagnosis of stage I-III hormone receptor-positive breast cancer * Postmenopausal * Currently receiving an aromatase inhibitor (anastrozole, letrozole, or exemestane) or within 5 years of initiation * Report joint pain that started or worsened after initiation of AI therapy * Report worst pain in the past week ≥3 on the BPI (0-10 scale) * Able to complete study procedures in English * Willing to be randomized to an intervention or attention control group and adhere to study procedures Exclusion Criteria: -An individual who meets any of the following criteria will be excluded from participation in this study: * Undergoing active cancer treatment (excluding endocrine therapy) * Uncontrolled cardiac or pulmonary disease that would limit safe participation * Currently engaged in regular structured moderate- or vigorous-intensity exercise (e.g., brisk walking, jogging/running, cycling, swimming, aerobic classes, or resistance training) totaling ≥150 minutes per week over the past 3 months * Currently participating in Tai Chi, yoga, Pilates, or other structured mind-body practice ≥2 times per week over the past 3 months * Joint pain due to inflammatory arthritic conditions * Recent surgery or joint injection within the past 4-6 weeks * Initiation or dose change of corticosteroids or opioids within the past 4 weeks * Planned discontinuation of AI therapy within the next 6 months * This study is limited to women with breast cancer, as \<1% of cases occur in men and data on AIIA in male patients are limited
Where it's running
-
Sidney Kimmel Cancer Center at Thomas Jefferson University
Philadelphia, Pennsylvania, United States Recruiting
Study contacts
- Principal investigator: Kuang-Yi Wen, PhD — Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
- Study coordinator: Kuang-Yi Wen, PhD
- Email: Kuang-Yi.Wen@Jefferson.edu
- Phone: 215-503-4623
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.