Understanding and Preventing Cortical Mechanisms of Chemotherapy-induced Peripheral Neuropathy

Description

Cohort 1: To track the onset and progression of a condition called chemotherapy-induced peripheral neuropathy (CIPN). Cohort 2: To track the onset and progression of a condition called chemotherapy-induced peripheral neuropathy (CIPN) and to test a certain type of experimental neuromodulation (stimulation of the brain) with a device called a closed-loop brain-computer interface (clBCI) to see if can help to prevent pain due to CIPN.

Conditions

Chemotherapy-induced Peripheral Neuropathy

Study Overview

Study Details

Study overview

Cohort 1: To track the onset and progression of a condition called chemotherapy-induced peripheral neuropathy (CIPN). Cohort 2: To track the onset and progression of a condition called chemotherapy-induced peripheral neuropathy (CIPN) and to test a certain type of experimental neuromodulation (stimulation of the brain) with a device called a closed-loop brain-computer interface (clBCI) to see if can help to prevent pain due to CIPN.

Understanding and Preventing Cortical Mechanisms of Chemotherapy-induced Peripheral Neuropathy

Understanding and Preventing Cortical Mechanisms of Chemotherapy-induced Peripheral Neuropathy

Condition
Chemotherapy-induced Peripheral Neuropathy
Intervention / Treatment

-

Contacts and Locations

Houston

MD Anderson Cancer Center, Houston, Texas, United States, 77030

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. Participants must have the ability to understand and read English, sign a written informed consent, and be willing to follow protocol requirements.
  • 2. ECOG Performance Status of 0-2;
  • 3. Willing to come to MD Anderson for the imaging sessions.
  • 4. Are 18 years of age or above.
  • 5. Have a diagnosis of breast cancer and who are scheduled to begin chemotherapy.
  • 6. will receive chemotherapy including doxorubicin, cyclophosphamide, docetaxel, or paclitaxel; 7) participants scheduled to receive six months of chemotherapy.
  • 1. Participants who are taking any antipsychotic medications.
  • 2. With active CNS disease, such as clinically evident metastases or leptomeningeal disease, dementia, or encephalopathy.
  • 3. Have ever been diagnosed with bipolar disorder or schizophrenia.
  • 4. Known, previously diagnosed peripheral neuropathy from causes other than chemotherapy; and
  • 5. A history of head injury or who have known seizure activity, or with a prior history of chemotherapy.
  • 6. Patients who will be administered ddAC-\>T.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

M.D. Anderson Cancer Center,

Sarah Prinsloo, PHD, PRINCIPAL_INVESTIGATOR, M.D. Anderson Cancer Center

Study Record Dates

2027-01-31