Wrist Worn Trackers for monitoring activity in brain tumour patients
- Conditions
- Primary and secondary brain tumoursCancerHigh-grade glioma (HGG) Low-grade glioma (LGG) Metastatic brain cancer
- Registration Number
- ISRCTN34351424
- Lead Sponsor
- Imperial College NHS Healthcare Trust
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
1. Primary or secondary brain tumours recently diagnosed and about to start treatment (unless matched healthy volunteers)
2. Patients with histology or clinically proven primary or secondary tumours who are fit to have radical treatment including surgery, radiotherapy or chemotherapy (unless matched healthy volunteers)
3. If being treated for recurrent tumour then at least 6 months must have elapsed since the completion of previous treatment (unless matched healthy volunteers)
4. Able to provide written informed consent
5. Fluent in English
6. Willing to undertake trial-specific measures, including wearing of and upload of data from wristband.
7. Aged over 18 years and 90 years or under
Patients do not need a smart phone to be eligible for this study
1. Patient undergoing WBRT
2. Patients with poor PS (PS3, 4) undergoing palliative treatments
3. Patients who have recently completed treatment (within 6 months) for primary or metastatic brain tumour
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method