None listed
Conditions
Brief summary
The purpose of this study is to assess the feasibility of collecting data on cognition over the course of treatment and recovery in patients with newly diagnosed aggressive lymphoma Who is it for? You may be eligible for this study if you are an adult who has been newly diagnosed with aggressive lymphoma, that is undergoing treatment at Austin Health. Study details All participants in this study will complete their usual treatment as prescribed by their doctor. Participants in this study will be assessed at three timepoints over the course of their treatment and recovery – one before treatment starts, one halfway, and one at the end of the treatment period. The assessment session will involve some tests to assess cognitive function and, in those participants willing to participate, a MRI brain scan and/or a PET/CT brain scan. It is hoped that this research will help determine if a larger study looking at cognitive function during chemotherapy for lymphoma is possible, adding to an underexplored area of cancer research.
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age greater than or equal to 18 years 2. Newly diagnosed aggressive lymphoma that requires standard chemotherapy treatment with curative intent at Austin Health. Including: • Hodgkin lymphoma • Diffuse large B cell lymphoma • Burkitt lymphoma • Transformed follicular lymphoma • Grade 3b follicular lymphoma 3. Able to read and comprehend English instructions. 4. Eastern Collaborative Oncology Group (ECOG) performance status less than or equal to 2
Exclusion criteria
Exclusion criteria: 1. Central Nervous System (CNS) lymphoma 2. Prior/planned cranial radiotherapy 3. An expected life expectancy < 12 months 4. Medical conditions that may compromise compliance or lead to prolonged hospitalisation 5. Documented history of or current substance abuse 6. Concurrent poorly controlled psychiatric illness.