Exercise Effect on Chemotherapy-Induced Neuropathic Pain

Last updated: August 5, 2024
Sponsor: Baltimore VA Medical Center
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Pain (Pediatric)

Pain

Ovarian Cysts

Treatment

aerobic exercise intervention

control group

resistive training

Clinical Study ID

NCT02991677
HP-00070946
  • Ages 21-70
  • All Genders

Study Summary

Chemotherapy-induced peripheral neuropathy (CIPN) continues to be a serious healthcare concern. It is painful, persistent, resistant to conventional pain therapies, and results in long-term suffering and decreased quality of life for many cancer survivors. The role of exercise to decrease CIPN-related neuropathic pain (CIPN-NP) will be investigated, with the goal of identifying the mechanisms associated with this therapeutic approach to manage CIPN-NP.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Diagnosis with cancer, stage I-IV

  • History of treatment with oxaliplatin, docetaxel, or paclitaxel, either alone or incombination with other agents

  • Completion of chemotherapy > 6 months < 1 year

  • Ability to walk on a treadmill

  • Medical clearance from oncologist or primary care provider

  • Presence of CIPN per National Cancer Institute Common Toxicity Criteria grade 1-3 (0-no signs/symptoms, 1-minor loss of function, 2-increased symptoms not interferingwith activities of daily living (ADLs), 3-severe symptoms interfering with ADL, 4-disabling, and 5 is death)

  • Score on Neuropathic Pain Scale >1

  • Age 21-70

Exclusion

Exclusion Criteria:

  • Denial of CIPN

  • Other motor/sensory neuropathy caused by other than chemotherapy (i.e.alcohol-related, autoimmune diseases, diabetes)

  • Coronary artery disease

  • History of >1 chemotherapy regimen

  • Musculoskeletal conditions which preclude participation in an exercise trainingprogram

  • Pregnancy

  • Regular exerciser, defined as >90 minutes per week of aerobic exercise and anyresistive training

Study Design

Total Participants: 60
Treatment Group(s): 3
Primary Treatment: aerobic exercise intervention
Phase:
Study Start date:
March 01, 2018
Estimated Completion Date:
December 31, 2025

Connect with a study center

  • Baltimore VA Medical Center

    Baltimore, Maryland 21201
    United States

    Site Not Available

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