Testing the Effects of Exercise on Chemotherapy-Induced Peripheral Neuropathy

Description

This phase II trial studies whether using exercise is better than the usual approach for treating chemotherapy-induced peripheral neuropathy (CIPN). CIPN occurs when chemotherapy damages the nerves communicating between the brain, spinal cord, and the rest of the body. The usual approach for treating CIPN is treatment with drugs that help reduce symptoms of other types of neuropathy (for example, from diabetes). However, these drugs do not treat all symptoms of CIPN. Exercise may help to reduce CIPN symptoms.

Conditions

Chemotherapy-Induced Peripheral Neuropathy

Study Overview

Study Details

Study overview

This phase II trial studies whether using exercise is better than the usual approach for treating chemotherapy-induced peripheral neuropathy (CIPN). CIPN occurs when chemotherapy damages the nerves communicating between the brain, spinal cord, and the rest of the body. The usual approach for treating CIPN is treatment with drugs that help reduce symptoms of other types of neuropathy (for example, from diabetes). However, these drugs do not treat all symptoms of CIPN. Exercise may help to reduce CIPN symptoms.

Multi-Center Randomized Controlled Phase II Trial of Exercise to Treat Chemotherapy-Induced Peripheral Neuropathy (CIPN)

Testing the Effects of Exercise on Chemotherapy-Induced Peripheral Neuropathy

Condition
Chemotherapy-Induced Peripheral Neuropathy
Intervention / Treatment

-

Contacts and Locations

Decatur

Cancer Care Specialists of Illinois, Decatur, Illinois, United States, 62526

Decatur

Decatur Memorial Hospital, Decatur, Illinois, United States, 62526

Decatur

Heartland NCORP, Decatur, Illinois, United States, 62526

Coon Rapids

Mercy Hospital, Coon Rapids, Minnesota, United States, 55433

Fridley

Unity Hospital, Fridley, Minnesota, United States, 55432

Saint Louis Park

Park Nicollet Clinic - Saint Louis Park, Saint Louis Park, Minnesota, United States, 55416

Saint Paul

Regions Hospital, Saint Paul, Saint Paul, Minnesota, United States, 55101

Saint Louis

Missouri Baptist Medical Center, Saint Louis, Missouri, United States, 63131

Rocky Mount

Nash General Hospital, Rocky Mount, North Carolina, United States, 27804

Dayton

Dayton Clinical Oncology Program, Dayton, Ohio, United States, 45459

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Have a diagnosis of cancer.
  • 2. Have received an infusion of neurotoxic chemotherapy within the past nine months (could still be on chemotherapy or have already completed chemotherapy; i.e., taxane-, platinum-, vinca alkaloid-, epothilone-, or proteasome inhibitor-based chemotherapy).
  • 3. Report one or more symptoms of CIPN at a level of ≥4 on the CIPN symptom inventory on the Screening Form.
  • 4. Have an ECOG Performance Status 0-1.
  • 5. Have at least six months life expectancy.
  • 6. Be at least 18 years of age.
  • 7. Be able to read and understand English.
  • 8. Be able to provide written informed consent.
  • 1. Have physical limitations (e.g., cardiorespiratory, orthopedic, central nervous system) that contraindicate participation in a low to moderate intensity home-based walking and progressive resistance exercise program, according to the patient's physician (e.g., oncologist, primary care) or physician's designee.
  • 2. Be identified as in the active or maintenance stage of exercise behavior per the Exercise Stages of Change Question on the Screening Form.
  • 3. Have planned surgery or radiation treatment during the course of the study (hormonal and biologic therapy is allowed).
  • 4. Have contraindications for MRI scanning, per the MRI safety screening procedures of the MRI facility to be utilized for this participant.
  • 5. Are pregnant or have plans to become pregnant during the course of the study. Documentation of pregnancy and use of contraception can be obtained from the medical record.
  • 6. Have a current or prior cancer in the central nervous system (spine, brainstem, brain) as this would interfere with assessments of brain functional connectivity.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Rochester NCORP Research Base,

Po-Ju Lin, PhD, MPH, PRINCIPAL_INVESTIGATOR, University of Rochester NCORP Research Base

Ian Kleckner, PhD, MPH, PRINCIPAL_INVESTIGATOR, University of Maryland, Baltimore

Study Record Dates

2026-01-02