Phase
Condition
Neoplasm Metastasis
Treatment
Fitbit
Neurocognitive Assessment
Questionnaire Administration
Clinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Measurable brain lesions noted on baseline MRI imaging
Graded Prognostic Assessment > 1.5
Body mass index (BMI) ≥18 kg/m2
Eastern Cooperative Oncology Group (ECOG) Performance status of 0-1 (0=participanthas either normal activity, 1= participant has some symptoms but is nearly fullambulatory)
Able and willing to follow prescribed diet intervention
Scheduled to receive SRS
Exclusion
Exclusion Criteria:• Undergoing whole brain radiation therapy
BMI <18 kg/m2
Pregnant or nursing women
Not willing to be randomized into either of the dietary interventions
Unable to provide Informed Consent
No previous diagnosis of small cell lung carcinoma
No previous or suspected leptomeningeal disease
Type 1 diabetes or insulin-dependent Type II diabetes
Abnormal renal function (GFR < 55 mL/min, creatinine >2.0, urinary albumin >1 g/day)Not MRI eligible
Study Design
Study Description
Connect with a study center
Ohio State University Comprehensive Cancer Center
Columbus, Ohio 43210
United StatesActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.