At-Home BCG Treatment for Bladder Cancer
This study is exploring a new way to deliver BCG (Bacillus Calmette-Guérin) treatment for bladder cancer at home. BCG is a type of immunotherapy often used for non-muscle invasive bladder cancer. The study aims to see if giving BCG at home is practical and effective. It will also use a chatbot, called BB-Bot, to help measure your symptoms and how you're feeling. You might be able to join if you are 18 or older and have completed intravesical treatment (treatment given directly into the bladder) for non-muscle invasive bladder cancer within the last year. The main goal is to see how well people stick to their BCG treatment plan after three months. The current recruitment status is unclear, and the study plans to enroll 50 participants.
- Study design
- This is a single-arm pilot study, meaning all participants will receive the same intervention. It aims to enroll 50 participants.
- What's involved
- Participants in the second group will use a conversational agent (chatbot) to track their symptoms and quality of life.
- Compensation
- Not stated in the trial record.
- Follow-up
- Adherence to BCG therapy will be measured at 3 months after the study starts.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Intravesical Treatment of Bladder Cancer at Home, Multi-modal Treatment Support
At a glance
Conditions
NCT07048496
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Abramson Cancer Center
Philadelphia, Pennsylvaniastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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Inclusion
Exclusion
What this trial measures
- Rate of adherence to BCG therapy at 3 months after study initiation3 months after study initiation
The primary outcome will be the rate of adherence to AUA guidelines for BCG therapy as measured by successful treatments of BCG compared to expected treatments. For each participant, adherence will be calculated both as the percentage of adherent doses, evaluable for study participants