CURATE.AI COR-Tx Trial for Post Brain Radiotherapy Patients
Cognitive Decline
About this trial
This is an interventional treatment trial for Cognitive Decline focused on measuring Oncology, Digital therapeutics, Cognitive evaluation, Digital diagnostic, Cognitive training, Phenotypic Personalised Medicine (PPM), Multi-Attribute Task Battery (MATB), Training intensity, Radiotherapy, CURATE.AI
Eligibility Criteria
Inclusion Criteria:
- Age >21 years.
- ECOG performance status 0 to 2.
- Patients with a neoplastic condition (benign or malignant) involving the brain or skull requiring radiotherapy (with or without chemotherapy).
- Patients with a life expectancy of at least 6 months.
Exclusion Criteria:
- Pregnant or breastfeeding women.
- Patients undergoing stereotactic radiosurgery (single fraction).
- Patients who are undergoing re-irradiation to the same area of the brain.
- Patients physically incapable of using computer tablet (either due to vision loss or dominant hand weakness)
- Patients who cannot understand spoken English language.
- Patients who are unable to give informed consent.
Sites / Locations
- National University HospitalRecruiting
- The N.1 Institute for Health (N.1), NUSRecruiting
Arms of the Study
Arm 1
Experimental
CURATE.AI
A cognitive evaluation and a Digital Diagnostic (DD) session performed anytime before radiotherapy will serve as the baseline. After the radiotherapy treatment, which can last between 1 to 6.5 weeks, patients will have a variable recovery time (0 to 4 weeks). Subsequently, patients will be subject to a cognitive evaluation and a DD session, right before starting the Digital Intervention (DI) training. This training will comprise ten weeks of DI (three 10-15 minute sessions per week). Patients will complete cognitive evaluations and DD sessions at the end of DI, and 16 and 32 weeks after the end of DI.