Radiation-induced cognitive impairment--from bench to bedside.
Dana Greene-Schloesser, Mike E Robbins
https://pubmed.ncbi.nlm.nih.gov/23095829Actively Recruiting
Led by Jona Hattangadi-Gluth · Updated on 2024-06-18
250
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying primary brain tumor patients who are undergoing fractionated radiation therapy to the brain. The study aims to understand how radiation affects brain tissue and cognitive function over time by using advanced neuroimaging and neurocognitive testing. The goal is to improve brain radiotherapy techniques to protect cognitive abilities by identifying vulnerable brain regions. Participants will undergo volumetric and diffusion magnetic resonance imaging (MRI) scans and complete neurocognitive tests at several times: before treatment, and at 3, 6, and 12 months after radiation therapy. Clinical information such as age, gender, tumor characteristics, and use of medications like steroids or chemotherapy will be recorded to support the analysis. During the study, participants will be monitored with brain MRI and cognitive assessments to track changes in brain structure and function. Researchers will measure imaging biomarkers such as brain volume and tissue integrity, along with memory, executive function, attention, language, fine motor skills, and quality of life. The total observation period includes assessments up to 12 months post-treatment, with some long-term quality of life evaluations extending to 5 years after therapy.
CONDITIONS
Longitudinal Prospective Study of Neurocognition & Neuroimaging in Primary BT Patients
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 12 months post-treatment
Participants undergo volumetric and diffusion brain MRI scans and complete neurocognitive tests to monitor changes over time after receiving fractionated partial brain radiation therapy.
4 visits at baseline (pre-treatment), 3 months, 6 months, and 12 months post-treatment
Total: 1 location
1
Moores Cancer Center
San Diego, California, United States, 92037
Actively Recruiting
S
Sheila Medina
J
Jona Hattangadi-Gluth, MD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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