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Recruiting NCT06389721

Understanding and Preventing Cortical Mechanisms of Chemotherapy-induced Peripheral Neuropathy

Conditions: Chemotherapy-induced Peripheral Neuropathy

Sponsor: M.D. Anderson Cancer Center

trial.available_in: БГ
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.
Description
Primary Objectives: Objective 1 (Primary Objective): to examine preliminary baseline and serial electrophysiological markers associated with the onset and development of CIPN by tracking brain activity and CIPN symptoms throughout chemotherapy treatment. Secondary Objectives: Objective 2 (Secondary Objective): To preliminarily evaluate whether a clBCI program can regulate changes in EEG that are associated with CIPN while participants are undergoing chemotherapy. Exploratory Objective: Explore whether there are associations between change in brain function and subjective report of CIPN.
Who can participate
Inclusion criteria: Objective 1 Inclusion 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. 6. will receive chemotherapy including doxorubicin, cyclophosphamide, docetaxel, or paclitaxel; Objective 2 Inclusion criteria: 1\) Inclusion criteria: Identical to Objective 1 and are willing to participate in the therapy sessions at their homes. Exclusion Criteria Objective 1 Exclusion criteria: 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. Objective 2 Exclusion criteria 1\) Same exclusion criteria as in Objective1. Medication usage will be tracked for patients in all groups. Once prescribed, participants must remain on a stable course of medications throughout the course of chemotherapy.
Interventions
Electroencephalogram (EEG)
DIAGNOSTIC_TEST
Locations 1
United States (1)
MD Anderson Cancer Center
Houston , Texas
Technical details
Status
Recruiting
Study type
OBSERVATIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
16.07.2024
Completion date
31.01.2027
Registry ID
NCT06389721
Source
clinicaltrials.gov
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