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 type | Interventional |
|---|---|
| Ages | 18 Years to 85 Years |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | University of Michigan Rogel Cancer Center Academic / other |
| Drugs / interventions | chemotherapy, immunotherapy, radiation |
| Locations | 1 site (Ann Arbor, Michigan) |
| Status | Recruiting |
| Started | September 10, 2026 |
| Main results expected | February 2028 |
| Study ends | February 2028 |
| Registry record updated | October 15, 2026 |
| Trial ID | NCT07673614 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
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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
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.