Recruiting

Observational Study

Sponsor:

University of Wisconsin, Madison

Code:

NCT07532083

Conditions

Oncology

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Study Details

Brief 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.

Conditions

Oncology

Study ID

NCT07532083

Start date

Feb 1, 2026

Status verified date

Apr, 2026

Completion date

Jan, 2027

Anticipated

Primary completion date

Jan, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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 eligible.
  • For the Patient Interview group only: Patients with radiographic disease progression will be excluded.

Study Design

Enrollment

2000 participants

Anticipated

Interventions and Outcome Measures

Arms

Patient Participants

  • Patient Baseline Survey (pre-implementation, at least 330 participants, up to 1900)
  • Patient Interviews (10-20 participants)
  • Patient Summary Feedback Survey (post-implementation, at least 330 participants, up to 1900)

Provider Participants

  • Provider Surveys (baseline, 1 month and 3 month post-implementation, 60 participants)
  • Provider Interviews (up to 20 participants)

Primary outcome measure

  • 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 [ Time Frame: up to 15 minutes ]
  • Perceived impact of scan-result-related patient queries on Provider Participant workload [ Time Frame: baseline, 3 months ]

Central Contacts and Locations

Central contacts

Supportive Oncology

608-263-6002supportiveoncology@uwcarbone.wisc.edu

Locations

UW Health

Recruiting

Madison, Wisconsin, United States, 53792

More Information

Sponsor

University of Wisconsin, Madison

Last update posted

Aug 5, 2026

Last verified

Apr, 2026

Keywords

  • Patient Care
  • Patient Communication
  • AI
  • Artificial Intelligence
  • Radiology
  • Imaging
  • Summary Reports

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Wisconsin, Madison on 2026-08-05.