About this trial
The goal of this clinical trial is to learn if a tailored intervention can help make it easier for adolescents and young adults with cancer to take their medications. The main questions the researchers are trying to answer are:
* Does the tailored intervention increase adherence? * Does the tailored intervention improve quality of life? * Does the tailored intervention reduce health care utilization?
The researchers will compare the tailored intervention to a uniform standard of care intervention (an intervention designed to be similar to what is currently happening in clinical care) to see if the tailored intervention works to improve adherence.
Participants will:
* Use an electronic pill bottle or box to store their medication * Participate in intervention sessions * Complete surveys before the intervention, after the intervention, and 6-months later
Eligibility criteria
Qualifiers
Patient is 15.00 to 24.99 years of age
Patient is diagnosed with cancer
Patient is prescribed an oral anticancer/antitumor agent or prophylaxis
Disqualifiers
Patient is not fluent in English
Patient evidences significant cognitive deficits
Patient's medical status or treatment precludes participation
Patient enrolled on a medical trial requiring medication storage in a trial-provided container
Trial design
Treatments tested in this trial
- Tailored Program
- Feedback Program (Uniform Standard of Care)
Treatment groups
Sponsors and collaborators
Children's Hospital Medical Center, Cincinnati
Lead sponsor
National Cancer Institute (NCI)
Collaborator
Seattle Children's Hospital
Collaborator
University of Kansas Medical Center
Collaborator
Columbia University
Collaborator