Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

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 typeInterventional
Ages18 Years and up
SexWomen only
Enrollment40 (estimated)
SponsorThomas Jefferson University
Academic / other
Locations1 site (Philadelphia, Pennsylvania)
StatusRecruiting
StartedJuly 27, 2026
Main results expectedJune 2027
Study endsJune 2029
Registry record updatedAugust 14, 2026
Trial IDNCT07737951 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.