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An Acupuncture Study for Breast Cancer Survivors With Joint Pain on Hormonal Therapies

Memorial Sloan Kettering Cancer Center (MSK) logo

Memorial Sloan Kettering Cancer Center (MSK)

Status

Enrolling

Conditions

Breast Cancer Stage II
Breast Cancer
Breast Cancer Stage IIIc
Breast Cancer Female
Breast Cancer Stage I
Breast Cancer Stage III
Breast Cancer Stage IIIB
Breast Cancer, Male

Treatments

Procedure: Acupuncture

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to see whether acupuncture is a practical (feasible) treatment for breast cancer survivors with joint pain on hormonal therapies.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • English- or Spanish-speaking
  • Black, Asian, and/or Hispanic women with a history of stage I, II, or III BC (transgender males are eligible to enroll)
  • No evidence of current BC disease
  • Receiving AI for at least 28 days with plan to continue for another 14 weeks
  • Worst pain rated ≥4 on a 0-10 scale in the preceding week
  • ≥15 days with pain in the past 30 days
  • Pain lasting ≥1 month
  • Pain attributed to AI as reported by the patient
  • Willing and able to complete questionnaires and other study activities
  • Willing and able to provide informed consent for the trial

Exclusion criteria

  • All Stage IV Cancer
  • Active oncological disease
  • Completed chemotherapy, surgery, or radiation <4 weeks prior to study
  • Pain attributed to inflammatory arthritis (e.g., rheumatoid arthritis, gout)
  • Procedures involving affected joints within the last month or planned in the next 14 weeks
  • Acupuncture use for pain in the past year
  • Implanted electronic device (e.g., pacemaker)

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Acupuncture
Experimental group
Description:
Participants will receive 10 weekly acupuncture treatments over 10 weeks.
Treatment:
Procedure: Acupuncture
Usual Care
No Intervention group
Description:
Participants will receive standard medical care, including pain medications and other treatments

Trial contacts and locations

2

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Central trial contact

Kevin Liou, MD; Pamela Drullinsky, MD

Data sourced from clinicaltrials.gov

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