Transcranial Direct Current Stimulation for the Treatment of Chemotherapy-Induced Peripheral Neuropathy in Cancer Survivors

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-85
SponsorUniversity of Michigan Rogel Cancer Center

About this trial

This clinical trial tests how well a type of non-invasive brain stimulation called transcranial direct current stimulation (tDCS) works to treat chemotherapy induced peripheral neuropathy (CIPN) in cancer survivors. CIPN is numbness, tingling, pain, and movement problems that can develop after chemotherapy as a result of changes to the nerves. A non-invasive form of brain stimulation called tDCS, applied to the area of the brain involved in sensation and movement, can temporarily improve the ability to detect vibration and temperature, as well as balance and walking, which may improve sensation and reduce pain in cancer survivors with CIPN.

Eligibility criteria

Qualifiers

18 to 85 years of age

Diagnosis of cancer, stages I-IV

Cancer survivor (not currently receiving chemotherapy, radiation, or immunotherapy)

Presence of CIPN defined as new, length-dependent numbness, tingling, and/or pain that developed with neurotoxic chemotherapy

Disqualifiers

Known brain metastases

Known neurological conditions aside from chemotherapy-induced peripheral neuropathy (CIPN)

History of brain or spinal surgery

Neuropathy other than CIPN

Trial design

Treatments tested in this trial

  • Sham Intervention
  • Survey Administration
  • Transcranial Direct Current Stimulation

Treatment groups

50 Participants
are divided into 2 treatment groups