Glioblastoma Remote Monitoring and Care - Research Protocol (NCT06129760) | Clinical Trial Compass
SuspendedNot Applicable
Glioblastoma Remote Monitoring and Care - Research Protocol
Stopped: PI decision
United States25 participantsStarted 2024-04-30
Plain-language summary
The purpose of this research is to learn more about how what the Apple watch measures, in terms of walking data, heart rate, breathing rate, and sleep habits, relates to how participants feel. During the course of the treatment, the symptoms participants experience change, and whether the Apple watch can detect these changes. Ultimately, this knowledge is being used to design proactive tools and signatures that can predict complications or symptom changes before they happen.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* newly-diagnosed or recurrent glioblastoma undergoing treatment or active surveillance
* at least 18 years of age at the time of study enrolment
* Karnofsky Performance Status (KPS) ≥ 70% at time of study enrolment
* able to comprehend informed consent form and provide informed consent
* access to patient or caregiver's own Apple iPhone to interface with watch application for documentation of symptoms
Exclusion Criteria:
* under 18 years of age at the time of study enrolment
* inability to give informed consent due to aphasia or other language barrier
* tattoos located on the skin of the wrist or forearm where the Apple Watch will be placed or other skin conditions preventing adequate sensor function
* inability to tolerate Apple Watch for at least 12 hours per day on at least 50% of days in a four-week period
* no access to patient or caregiver Apple iPhone to document symptoms
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.