A Collaborative Intervention for Improving Cancer Pain Management in Cancer Survivors

Recruiting N/A Interventional Study
Hematopoietic and Lymphoid System Neoplasm Malignant Solid Neoplasm Hematopoietic and Lymphatic System Neoplasm
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
660 (estimated)
Sponsor
Mayo Clinic · Other
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About This Trial
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 f…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * A qualifying liquid or solid cancer diagnosis with visits at a participating Mayo site in the past 15 years * Including malignant hematology * Lymphoma * Myeloma * Chronic leukemias * Age \>= 18 * Numeric Rating Scale (NRS) pain score of \>= 5/10 * Pain that de…
Contacts

Clinical Trials Referral Office

507-293-1043

mayocliniccancerstudies@mayo.edu

CONTACT

Josiah Lulf

507-538-7991

Lulf.Josiah@mayo.edu

CONTACT