RecruitingNot ApplicableNCT07794098

Intelligent Sexual Health Information Support System for Gynecological Cancer Patients

Intelligent Sexual Health LillyBot Information Support System for Gynecological Cancer Patients: Development, Test and Evaluation of Longitudinal Effects

Sponsor

Chang Gung Memorial Hospital

Enrollment

90 participants

Start Date

Jun 17, 2026

Study Type

INTERVENTIONAL

Conditions

Sexual and Reproductive Health Gynecologic Cancer Survivors

Summary

This study aims to develop the LillyBot Smart Sexual Health Consultation System, designed to meet the sexual health learning and consultation needs of gynecological cancer (GC) patients in Taiwan. Grounded in the Transtheoretical Model (TTM), this system integrates AI chatbot technology and mobile health (mHealth) to provide real-time, personalized sexual health education and consultations, ultimately improving the overall sexual well-being of GC patients.

Eligibility

Sex: FEMALEMin Age: 20 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Intelligent Sexual Health Information Support with Proactive Nurse Researcher Contact, Intelligent Sexual Health Information Support with Safety-Triggered Nurse Researcher Contact, and others for people with gynecologic cancer survivors and sexual and reproductive health. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 20 Years to 70 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERIntelligent Sexual Health Information Support with Proactive Nurse Researcher Contact

The experimental group A will receivereceive the intelligent sexual health information support system along with proactive nurse researcher (registered nurse) contact.Data will be collected at baseline (T0), one month post-intervention (T1), and three months (T2) to evaluate the intervention's effectiveness.

OTHERIntelligent Sexual Health Information Support with Safety-Triggered Nurse Researcher Contact

The experimental group B will receive the intelligent sexual health information support system with nurse researcher contact only upon a triggered safety alert.Data will be collected at baseline (T0), one month post-intervention (T1), and three months (T2) to evaluate the intervention's effectiveness.

OTHERUsual Gynecologic Cancer Care

The control group will receive Usual Gynecologic Cancer Care.Data will be collected at baseline (T0), one month post-intervention (T1), and three months (T2) to evaluate the intervention's effectiveness.

Locations(1)

Cheng Gung Memorial Hospital

Taoyuan, Guishan, Taiwan

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NCT07794098

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