Clinical trial Recruiting at 1 site Observational Ages 18 and up Women only

GYN-AIDE: AI-Driven Education to Help Gynecologic Cancer Patients

Official title: GYN-AIDE: Gynecologic Oncology Navigation Through AI-Driven Education

Run by University of Southern California · NCT07279571 · Data updated 2026-11-12

This study tests an AI chatbot to help endometrial cancer patients learn about care and HPV vaccination, and to see if using the chatbot influences vaccination uptake in a gynecologic oncology clinic.

More Gynecologic Disease trials

Quick facts

Study typeObservational
Ages18 Years and up
SexWomen only
Enrollment48 (estimated)
SponsorUniversity of Southern California
Academic / other
Locations1 site (Los Angeles, California)
StatusRecruiting
StartedJune 12, 2026
Main results expectedJune 9, 2027
Study endsJune 9, 2028
Registry record updatedAugust 6, 2026
Trial IDNCT07279571 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) seen in the LA General gynecologic oncology clinic who speak English or Spanish and are willing to consent; eligible for HPV vaccination (pilot intervention age under 46).

Probably not a fit

Patients who do not wish to use AI education or who are not eligible for HPV vaccination may not experience additional benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study explores how patients with gynecologic disease obtain cancer-care information and their satisfaction with AI-based education. It has two aims: first, to test an AI chatbot for HPV vaccine counseling and measure patient satisfaction, and second, to see if introducing the chatbot affects HPV vaccination rates among new gynecologic oncology patients. Participants complete surveys to describe their information sources, experiences with the chatbot, and attitudes toward artificial intelligence in education. Eligible participants include adults seen at the LA General gynecologic oncology clinic who speak English or Spanish and provide informed consent. The study is non-interventional and conducted at Los Angeles General Medical Center with USC as lead sponsor and NCI collaboration.

Why it matters

Potential benefit: If successful, patients may receive clearer information and higher HPV vaccination rates through AI-assisted counseling.

How similar studies have gone: Prior work has shown AI-based educational tools can impact patient knowledge and engagement, but results vary by setting and condition, making this approach exploratory in this specific gynecologic oncology context.

Who can join: the full rules

Show full inclusion / exclusion criteria
AI-chatbot Evaluation (Aim 1):

Inclusion Criteria:

* Patient of the LA General gynecologic oncology clinic
* Age 18 years or older
* Previously obtained the HPV vaccination (initial chatbot evaluation)
* Eligible for HPV vaccination (pilot intervention; age \<46)
* Willing and able to provide informed consent

Exclusion Criteria:

* Patients who do not speak English or Spanish
* Patients who do not provide informed consent

HPV vaccination rate (Aim 2):

Inclusion Criteria:

* Patient of the LA General gynecologic oncology clinic
* Age 18 years or older
* Obtained the HPV vaccine

Exclusion Criteria:

* None

Where it's running

  • Los Angeles General Medical Center
    Los Angeles, California, United States
    Recruiting

Study contacts

  • Principal investigator: Xiaoyue M Guo — University of Southern California

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.