CTNow: Education Program for Rural Cancer Patients
This study, called CTNow, is testing a program designed to help rural cancer patients and their doctors learn more about cancer clinical trials. The program involves multimedia educational videos for patients and workshops via Zoom for healthcare providers. The goal is to see if these educational tools can increase patients' understanding and knowledge of clinical trials over 18 months. You may be able to join if you are 18 or older, have been diagnosed with any cancer, and can read, write, and speak English. You can be currently receiving treatment, have received treatment, or be starting treatment within 90 days. The study plans to enroll 50 participants, but its current recruitment status is unclear.
- Study design
- This is an interventional study that plans to enroll 50 participants. It is testing an educational program for both patients and providers.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study will measure changes in patient awareness and knowledge of clinical trials at 18 months.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
CTNow: A Clinical Trials Education Program for Rural Cancer Patients and Oncology Providers
At a glance
Conditions
Where it's being run
3 sites across 1 statesStudy leadership
- Izumi Okado, PhD · PRINCIPAL_INVESTIGATOR · University of Hawaii Cancer Research Center
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Change in patients' awareness and knowledge of clinical trials18 months
Participants will complete a 12-item awareness and knowledge of clinical trials questionnaire at baseline and post-intervention. Items are reported on a Likert-type scale , with higher scores indicating greater knowledge. A paired t-test will be used to evaluate whether there is a statistically significant difference in pre- and post-intervention scores on patients' knowledge of clinical trials.