Integrative Medicine for Pain in Patients With Advanced Cancer Trial (IMPACT)

Last updated: October 8, 2025
Sponsor: Memorial Sloan Kettering Cancer Center
Overall Status: Active - Not Recruiting

Phase

2

Condition

Acute Pain

Cancer Pain

Pain

Treatment

Acupuncture

Massage

Clinical Study ID

NCT04095234
19-341
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to compare the long-term effectiveness of acupuncture versus massage in people living with advanced cancer. The study will test how the two approaches compare in helping people with pain and its related symptoms and improving quality of life.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age ≥ 18 years or older

  • Having a diagnosis of the following: stage III or IV lung cancer; any stagepancreatic cancer; unresectable cholangiocarcinoma; unresectable liver cancer;unresectable ampullary or peri-ampullary cancer or other stage IV gastrointestinalcancer; stage III or IV ovarian or fallopian tube cancers or other stage IVgynecologic cancer; stage IV breast cancer; stage III testicular cancer; stage IVgenitourinary cancer; stage III or IV sarcoma; stage IV melanoma; stage III or IVhead/neck cancer; stage IV endocrine cancer; or hematological malignancies (lymphoma, myeloma, and leukemia)

  • Be ambulatory (Karnofsky functional score of ≥ 60)

  • Having musculoskeletal pain, defined as regional (joints, extremities, back, neck)or more generalized (fibromyalgia or chronic widespread pain); Patients with aneuropathic component to their pain that involves the extremities or back will beeligible.

  • Having musculoskeletal pain for at least 1 month

  • Having had pain for at least 15 days in the preceding 30 days

  • Having a pain rating of 4 or greater in worst pain on a 0-10 numerical rating scalein the preceding week

  • Having an expected prognosis of greater than six months as judged by the treatingoncologist or study physician

Exclusion

Exclusion Criteria:

  • Having a platelet count <15,000

  • Cognitive impairment precluding response to study assessments

  • Unwilling to accept random assignment

  • Unwilling to commit to the 26-week study time period

  • Have non-musculoskeletal pain syndromes (headache, facial pain, chest pain, visceralabdominal pain) if these are the sole source of pain but can be present as co-morbidconditions as long as a patient has a primary musculoskeletal pain condition definedas above.

Study Design

Total Participants: 300
Treatment Group(s): 2
Primary Treatment: Acupuncture
Phase: 2
Study Start date:
September 17, 2019
Estimated Completion Date:
September 30, 2026

Connect with a study center

  • Baptist Alliance MCI

    Miami, Florida 33143
    United States

    Site Not Available

  • Baptist Alliance MCI

    Miami 4164138, Florida 4155751 33143
    United States

    Site Not Available

  • Memorial Sloan Kettering Basking Ridge (All Protocol Activities)

    Basking Ridge, New Jersey 07920
    United States

    Site Not Available

  • Memorial Sloan Kettering Monmouth (All Protocol Activities)

    Middletown, New Jersey 07748
    United States

    Site Not Available

  • Memorial Sloan Kettering Bergen (All Protocol Activities)

    Montvale, New Jersey 07645
    United States

    Site Not Available

  • Memorial Sloan Kettering Basking Ridge (All Protocol Activities)

    Basking Ridge 5095409, New Jersey 5101760 07920
    United States

    Site Not Available

  • Memorial Sloan Kettering Monmouth (All Protocol Activities)

    Middletown 5101170, New Jersey 5101760 07748
    United States

    Site Not Available

  • Memorial Sloan Kettering Bergen (All Protocol Activities)

    Montvale 5101361, New Jersey 5101760 07645
    United States

    Site Not Available

  • Memorial Sloan Kettering Commack (All Protocol Activities)

    Commack, New York 11725
    United States

    Site Not Available

  • Memorial Sloan Kettering Westchester (All Protocol Activities)

    Harrison, New York 10604
    United States

    Site Not Available

  • Memorial Sloan Kettering Cancer Center (All Protocol Activities)

    New York, New York 10065
    United States

    Site Not Available

  • Memorial Sloan Kettering Nassau (All Protocol Activities)

    Uniondale, New York 11553
    United States

    Site Not Available

  • Memorial Sloan Kettering Commack (All Protocol Activities)

    Commack 5113412, New York 5128638 11725
    United States

    Site Not Available

  • Memorial Sloan Kettering Westchester (All Protocol Activities)

    Harrison 5120095, New York 5128638 10604
    United States

    Site Not Available

  • Memorial Sloan Kettering Cancer Center (All Protocol Activities)

    New York 5128581, New York 5128638 10065
    United States

    Site Not Available

  • Memorial Sloan Kettering Nassau (All Protocol Activities)

    Uniondale 5141927, New York 5128638 11553
    United States

    Site Not Available

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