Clinical trial Recruiting at 1 site Interventional Ages 18 to 85

Non-invasive brain stimulation to help chemotherapy-induced nerve problems in cancer survivors

Official title: Improving Sensorimotor Function in CIPN: A Randomized, Sham Controlled, Double Blinded, Crossover Mechanistic Trial of Transcranial Direct Current to the Sensorimotor Cortex

Run by University of Michigan Rogel Cancer Center · NCT07673614 · Data updated 2026-11-12

This trial tests whether a gentle brain stimulation method (tDCS) can help reduce numbness, tingling, and pain from CIPN in cancer survivors who are not currently in treatment.

Quick facts

Study typeInterventional
Ages18 Years to 85 Years
SexAll
Enrollment50 (estimated)
SponsorUniversity of Michigan Rogel Cancer Center
Academic / other
Drugs / interventionschemotherapy, immunotherapy, radiation
Locations1 site (Ann Arbor, Michigan)
StatusRecruiting
StartedSeptember 10, 2026
Main results expectedFebruary 2028
Study endsFebruary 2028
Registry record updatedOctober 15, 2026
Trial IDNCT07673614 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18-85 with a cancer history (stages I-IV) and CIPN from prior neurotoxic chemotherapy, able to walk unassisted, English-speaking, not currently in active cancer therapy.

Probably not a fit

Individuals with brain metastases, non-CIPN neuropathies, significant sensory deficits, or contraindications to tDCS may not experience benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study uses transcranial direct current stimulation (tDCS) to see if stimulating the brain area related to sensation and movement can improve CIPN symptoms in cancer survivors. Participants may also complete surveys and undergo sham stimulation to compare effects. The trial targets adults with CIPN from prior neurotoxic chemotherapy and who can walk unassisted. It excludes people with brain metastases, other neurological conditions, or contraindications to tDCS. The study is sponsored by the University of Michigan Rogel Cancer Center and conducted at Ann Arbor, Michigan.

Why it matters

Potential benefit: If successful, participants may experience reduced CIPN symptoms and improved balance and walking ability.

How similar studies have gone: Prior non-invasive brain stimulation approaches have shown potential in addressing CIPN, but results vary and broader validation is needed.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 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
* CIPN20 score ≥ 20
* Able to walk unassisted
* Proficient in English

Exclusion Criteria:

* Known brain metastases
* Known neurological conditions aside from chemotherapy-induced peripheral neuropathy (CIPN)
* History of brain or spinal surgery
* Neuropathy other than CIPN
* Significant hearing or vision deficits
* Vestibulopathy
* Currently receiving chemotherapy, radiation therapy, or immunotherapy
* Contraindications to transcranial direct current stimulation (tDCS), including recent seizures
* Presence of metallic objects in the head
* Presence of specific implanted medical devices (e.g., deep brain stimulator, cochlear implant, vagus nerve stimulator, spinal cord stimulator, pacemakers, and intracardiac devices)
* Active scalp dermatological conditions

Where it's running

  • University of Michigan Rogel Cancer Center
    Ann Arbor, Michigan, United States
    Recruiting

Study contacts

  • Principal investigator: Brendan L McNeish — University of Michigan Rogel Cancer Center
  • Study coordinator: Eshaka Eshwar
  • Email: eshaka@med.umich.edu
  • Phone: 734-232-5901

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.