Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06198010

A Collaborative Intervention for Improving Cancer Pain Management in Cancer Survivors

Led by Mayo Clinic · Updated on 2026-04-13

660

Participants Needed

3

Research Sites

185 weeks

Total Duration

On this page

Sponsors

M

Mayo Clinic

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This clinical trial tests a collaborative pain management intervention (ASCENT) for improving cancer pain in cancer survivors. Cancer pain is prevalent, under-treated, and remains a major cause of suffering, impairment, and disability for millions of Americans. Individual pain interventions and care models show promise for cancer pain in controlled settings. All cancer survivors stand to benefit from electronic health record innovations, as they can experience profound pain outcomes, including marked under- and over-prescribing of opioids. Digitally facilitated solutions are especially helpful and can be customized to address patient needs. The ASCENT intervention provides patients with an educational guide that describes techniques for addressing cancer pain, and uses community health workers and pain care managers to coach patients through a personalized pain management plan. This study may help researchers learn how pain management strategies can improve cancer pain and lower risk of opioid exposure and dependency in cancer survivors.

CONDITIONS

Official Title

A Collaborative Intervention for Improving Cancer Pain Management in Cancer Survivors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • A liquid or solid cancer diagnosis with visits at a Mayo Clinic site in the past 15 years, including malignant hematology such as lymphoma, myeloma, or chronic leukemias
  • Age 18 years or older
  • Numeric Rating Scale (NRS) pain score of 5 or higher
  • Pain developed or worsened after cancer diagnosis
  • Meet the description of rural or Hispanic or both
Not Eligible

You will not qualify if you...

  • Patient Health Questionnaire - 8 (PHQ8) score of 13 or higher
  • Enrollment in hospice
  • Residence in skilled nursing, inpatient rehabilitation, or long-term care facility
  • Palliative Care or Pain Clinic visits in past or upcoming two months
  • Any mention of hospice referral in oncology notes
  • Confined to bed or chair more than one-third of waking hours
  • Currently homeless or do not feel safe at home
  • New or worsening chest pain, tightness, or pressure
  • Back pain with new/worsening weakness, bowel/bladder control loss, or walking difficulty
  • Lightheadedness, inability to keep down food or fluids, or vomiting blood or dark material
  • New/worsening headaches with vision changes, nausea, balance, or speech problems
  • Positive screen for monthly or more frequent non-cannabis drug use
  • Unable to participate due to medical or psychological reasons

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Mayo Clinic in Arizona

Scottsdale, Arizona, United States, 85259

Actively Recruiting

2

Mayo Clinic in Florida

Jacksonville, Florida, United States, 32224-9980

Actively Recruiting

3

Mayo Clinic in Rochester

Rochester, Minnesota, United States, 55905

Actively Recruiting

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Research Team

C

Clinical Trials Referral Office

CONTACT

J

Josiah Lulf

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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