RecruitingNCT07532083
Implementing AI-Assisted, Patient-Friendly Imaging Report Summaries to Enhance Oncology Care Delivery
Sponsor
University of Wisconsin, Madison
Enrollment
2,000 participants
Start Date
Feb 1, 2026
Study Type
OBSERVATIONAL
Conditions
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.
Eligibility
Min Age: 18 Years
Inclusion Criteria11
- 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.
- 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 Criteria3
- 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 eligible.
- For the Patient Interview group only: Patients with radiographic disease progression will be excluded.
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Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07532083
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