Brain Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
Patients:
- People who receive care at the Virginia Commonwealth University Neuro-Oncology clinic
- People who have a confirmed primary brain tumor diagnosis, either through a tissue sample (biopsy) or a specialist's review of brain scans
- People who show reduced ability in at least one area of thinking or memory, based on specific cognitive tests used by the trial
- People whose estimated baseline intellectual ability falls above a certain threshold, as measured by a standard test (confirm with trial site)
- People who are at least one month past brain surgery and/or radiation therapy, if they had either of these treatments
- People aged 18 or older
- People who primarily speak English
Caregivers:
- People who are enrolling alongside a patient who meets the criteria above
- People aged 18 or older
- People who primarily speak English
Who may not be able to join:
Patients:
- People with severe thinking or memory difficulties that would prevent them from taking part, including severe difficulty with speech or language, or an inability to understand and agree to participate
- People who are unable to attend weekly video appointments
- People who have significant sleep problems that they find more disruptive than their thinking or memory difficulties
- People who are less than one month past brain surgery and/or radiation therapy
- People without a stable internet connection or ability to use video-calling software (note: the trial will provide a tablet device if a participant does not have a suitable one)
- People who have metal in their body, as this could be unsafe during the MRI scan
- People who are pregnant, as the MRI scan may carry risks to an unborn baby
Caregivers:
- No specific exclusion criteria listed for caregivers (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Sarah Braun, Ph.D, Virginia Commonwealth University
Phone: 804-628-7028
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Assess the feasibility of the C-SMART and BE Well protocols in brain tumor patients- Eligibility Rate; Assess the feasibility of the C-SMART and BE Well protocols in brain tumor patients - Enrollment Rate; Assess the feasibility of the C-SMART and BE Well protocols in brain tumor patients -- retention rate; Assess the acceptability of the C-SMART and BE Well protocols in brain tumor patients -- intervention completion rate; Assess the acceptability of the C-SMART and BE Well protocols in brain tumor patients - Participant satisfaction ratings; Assess the acceptability of the C-SMART and BE Wel...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.