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Recruiting

NCT Number: NCT06814977

An Acupuncture Study for Cancer Survivors With Joint Pain

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

Recruiting

Interested in participating?

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Memorial Sloan Kettering Cancer Center (All protocol activites), New York, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Acupuncture

Procedure

Acupuncture is a non-pharmacological intervention that does not involve the use of any therapeutic agents or devices. Participants will receive 10 weekly treatments over 10 weeks.

Primary outcomes

  1. Study feasibility as measured by rates of enrollment

    Time frame: 1 year

    The primary purpose of this study is to determine the feasibility of studying an acupuncture intervention for chronic musculoskeletal pain in racially/ethnically diverse, community-based cancer survivors.

Study contacts

Contact information is provided by the study sponsor or research team.

Kevin Liou, MD

CONTACT

[email protected]

646-608-8563

Pamela Drullinsky, MD

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Memorial Sloan Kettering Cancer Center

Other

Registry information

Official study title

Researching the Implementation of Acupuncture for Chronic Musculoskeletal Pain in Diverse Underserved Cancer Survivors (ReIMAGINE)

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Feb 7, 2025
Registry last updated
Oct 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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