Implementing AI-Assisted, Patient-Friendly Imaging Report Summaries to Enhance Oncology Care Deli… (NCT07532083) | Clinical Trial Compass
RecruitingNot Applicable
Implementing AI-Assisted, Patient-Friendly Imaging Report Summaries to Enhance Oncology Care Delivery
United States2,000 participantsStarted 2026-02-01
Plain-language summary
The implementation of the AI-assisted radiology summary tool into clinical workflows is being conducted as part of a standard-of-care quality improvement (QI) initiative at UW Health. The evaluation of this tool's impact via structured feedback from patients and providers is being undertaken as a prospective research study.
Who can participate
Age range18 Years
SexALL
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 (Patient Participants):
* Age 18 years or older
* Having a current or prior cancer diagnosis (any cancer type)
* Has active access to the UW Health MyChart patient portal.
* Receiving care at UW Health within the Division of Hematology, Medical Oncology and Palliative Care or Department of Gynecologic Oncology.
* Undergoing imaging studies (such as CT, MRI, or PET scans) as part of routine cancer care.
* Willing and able to complete electronic REDCap surveys.
* For interview participation: willing to participate in a 30-45-minute phone or video interview.
Inclusion Criteria (Provider Participants): Cancer care providers will be eligible to participate in this study if they meet all of the following criteria:
* Faculty physician (MD or DO) practicing in the Division of Hematology, Medical Oncology and Palliative Care or Department of Gynecologic Oncology at UW Health.
* Involved in reviewing, discussing, or sharing imaging results with patients.
* Planned to gain access to the AI-assisted, patient-friendly imaging summary tool as part of clinical implementation.
* Willing and able to complete electronic surveys or participate in a brief interview (\~30 minutes).
Exclusion Criteria (Patients):
* Are unable to provide informed consent due to cognitive impairment or other limitations, as determined by the clinical or study team.
* Enrolled in an active interventional clinical trial. Patients on biospecimen, registry, or non-interventional studies are eligi…
What they're measuring
1
Proportion of Patient Participants who report the information presented in their results is "Somewhat easy to understand" or "Very easy to understand" when reviewed by themselves
Timeframe: up to 15 minutes
2
Perceived impact of scan-result-related patient queries on Provider Participant workload