Actively Recruiting
A Study of the ApricityCare Program for Early Detection and Management of Treatment-Related Adverse Events in Patients With Cancer
Led by M.D. Anderson Cancer Center · Updated on 2025-12-30
425
Participants Needed
1
Research Sites
149 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To evaluate the rate of therapy discontinuation due to toxicity (side effects) among participants with cancer using ApricityCare. Investigators want to learn if identification of early clinical signs of irAEs with timely treatment can prevent severity progression and reduce treatment discontinuation.
CONDITIONS
Official Title
A Study of the ApricityCare Program for Early Detection and Management of Treatment-Related Adverse Events in Patients With Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years of age or older
- Confirmed diagnosis of cancer
- Patients with prostate, kidney, and/or bladder cancer with either localized or metastatic disease for Part 1 (Run-in Phase)
- Metastatic cancer patients for Part 2 (Expansion Phase)
- Planned to receive systemic anti-cancer therapy
- Ability to understand and willingness to sign a written informed consent
- Ability to speak, read, and understand English, Spanish, Mandarin, or Cantonese Chinese
- Ownership of a smartphone and willingness to use it as outlined in the protocol
You will not qualify if you...
- Any medical, psychological, or social condition that the investigator believes would prevent participation in the study (pregnancy is allowed)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
MD Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
B
Bilal A Siddiqui, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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