Quality of Life Clinical Trial
— CoDeB-RadOfficial title:
Measuring and Mapping Cognitive Decline After Brain Radiosurgery: a Pilot Study
Background Stereotactic Radiosurgery (SRS) is a localised radiotherapy treatment for patients with brain metastases or other benign tumours in the brain, like meningiomas. We do not currently know if, or how much, SRS affects brain function. Patients with brain tumours do not get tested routinely for their brain function. Understanding short- and long-term side-effects is important for SRS. Brain metastases patients have short life expectancies (6-months to 1-year). However, meningioma patients can live 10 years or more. SRS is used to treat both. We will use the Montreal Cognitive Assessment (MoCA) to test your brain function. We will use quality-of-life questionnaires QLQ-C30 and BN20. These are specific for patients with brain cancer. They include questions about physical and mental wellbeing. Why is it important This study aims to identify areas in the brain that relate to changes in brain function after SRS. These areas can then have the radiation dose reduced to them in future patients, hoping to minimise side-effects. Research Question Which regions of the brain contribute to a decline in brain function following SRS. Study Design This is a single centre observational study with prospective and retrospective collection of data. This study will look at two groups of patients: Group1: Patients will complete the MoCA and two quality-of-life questionnaires before your treatment and every 3 months for a year. Group2: Patients will complete the MoCA and two quality-of-life questionnaires once. We will use these tests, your MRI scans and your SRS treatment plan to identify areas of the brain that are responsible for any problems with your brain function. The participants for Group 1 will be recruited from the SRS Clinics, at City Campus, Nottingham University Hospitals NHS Trust. The participants for Group 2 will be identified through the Mosaiq Oncology Information System. This pilot study is funded by the Midlands Mental Health and Neurosciences Network.
Status | Not yet recruiting |
Enrollment | 80 |
Est. completion date | February 28, 2026 |
Est. primary completion date | February 28, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion criteria Prospective Cohort Patients will be eligible for inclusion only if ALL of the following criteria apply: - Age: above 18 years, no upper limit - Diagnosis of brain metastases or meningioma, where the treatment is going to be stereotactic radiosurgery - Karnofsky Performance Status (KPS) =70 - Established diagnosis of cancer with absent or controllable primary disease - Tumour volume of less than 20cc - Life expectancy of more than 6 months - Able to give informed consent Exclusion criteria Prospective Cohort - Previous RT to the brain, including SRS - Previous surgery to the brain - Not willing or not able to give informed consent Inclusion criteria Retrospective Cohort Patients will be eligible for inclusion only if ALL of the following criteria apply: - Age: above 18 years, no upper limit - Diagnosis of meningioma - Previous SRS treatment at least 1 year prior to inclusion in the study - Most recent MRI scan (within 1 year) shows stable appearances - Able to give informed consent Exclusion criteria Retrospective Cohort - Previous RT to the brain, excluding SRS - Previous surgery to the brain - Not willing or not able to give informed consent |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Nottingham University Hospitals NHS Trust | Nottingham | Nottinghamshire |
Lead Sponsor | Collaborator |
---|---|
University of Nottingham | Wellcome Trust |
United Kingdom,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Areas of the brain related to neurocognitive function | • Geographical correlation of areas in the brain with change in neurocognitive function as identified by Voxel based lesion symptom mapping | 6 months | |
Other | Identification of radiosensitive structures in the brain | • Identification of brain structures most affected by radiation via differences in the cognitive testing. | 6 months | |
Primary | Change from Baseline to neurocognitive function and Quality of Life at 6 months | Significant changes in neurocognitive function and Quality of Life at 6 months compared to baseline.The scale ranges from 0-100 with 0 signifying a worse quality of life and 100 signifying excellent quality of life for the participants. The cognitive function scale ranges from 0-30 with 30 signifying non-impaired cognitive function. | 6 months | |
Primary | Doses related to neurocognitive symptoms | • Doses above which the lesion symptom mapping identifies areas of the brain relevant to neurocognitive symptoms at 6 months. | 6 months | |
Secondary | Recruitment feasibility | The number of patients screened versus the number of patients recruited will be recorded along with any reasons for non-participation | 1.5 years | |
Secondary | Patient reported symptoms vs symptoms identified by neurocognitive testing | • Do patient reported symptoms relate to those identified from neurocognitive testing. | At baseline and every 3 months |
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