ClinicalTrials.Veeva

Menu

An Acupuncture Study for Cancer Survivors With Joint Pain

Memorial Sloan Kettering Cancer Center (MSK) logo

Memorial Sloan Kettering Cancer Center (MSK)

Status

Enrolling

Conditions

Cancer Survivor

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 cancer survivors with joint pain.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • English- or Spanish-speaking adults
  • Non white or Hispanic women with a prior cancer diagnosis
  • Stable oncological disease or no evidence oncological of disease per clinical documentation or clinician assessment
  • 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
  • Willing and able to complete questionnaires and other study activities
  • Willing and able to provide informed consent for the trial

Exclusion criteria

  • Completed active treatment (chemotherapy, surgery, radiation, transplantation) <4 weeks prior to study
  • Maintenance therapies are allowed
  • Pain attributed to inflammatory arthritis (e.g., rheumatoid arthritis, gout)
  • Other non-musculoskeletal pain syndromes (eg, headache, visceral abdominal pain, neuropathic pain) can be present as comorbid conditions if the patient reports musculoskeletal pain as the primary source of pain
  • Procedures involving affected joints within the last month or planned in the next 14 weeks
  • Acupuncture use for pain in the past three months
  • 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

Loading...

Central trial contact

Pamela Drullinsky, MD; Kevin Liou, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems