ACTIVE_NOT_RECRUITING

Use of Artificial Intelligence by Urogynecologic Patients

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to learn about how Urogynecology patients use Artificial Intelligence (AI) Chatbots like ChatGPT, and how it affects healthcare decision making. The main question\[s\] it aims to answer are: * How does the AI Chatbot affect participants' understanding of diagnoses and participant satisfaction with a urogynecology consultation? * How accurate is the chatbot-provided diagnosis and counseling information? Participants will be asked to use the ChatGPT chatbot and ask it questions about the main problem the participant is seeing the doctor for, and will also be asked to fill out some questionnaires. Researchers will compare using the Chatbot before the visit, after the visit, or not at all to see if the way participants understand the information changes based on timing of use.

Official Title

Use of Artificial Intelligence by Patients for Understanding of Diagnosis of Urogynecologic Conditions and Its Role in Treatment Decisions

Quick Facts

Study Start:2024-07-22
Study Completion:2025-04-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06481436

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 89 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * female
  2. * presenting for their initial evaluation by a urogynecology physician for one of the following:
  3. * urinary incontinence (UI)
  4. * lower urinary tract symptoms (LUTS)
  5. * pelvic organ prolapse (POP)
  6. * greater than or equal to18 and less than or equal to89 years old
  7. * any race/ethnicity
  8. * able to read or speak English or Spanish
  9. * able/willing to consent to participate
  1. * male
  2. * primary presenting problem other than UI, LUTS, or POP
  3. * non-English or non-Spanish speaking
  4. * pregnant or lactating, as this may affect patient treatment counseling
  5. * unable/unwilling to consent to participate

Contacts and Locations

Principal Investigator

Nicole J Wood, MD
PRINCIPAL_INVESTIGATOR
Hartford Hosptial Division of Urogynecology
Elena Tuntisky-Bitton, MD
PRINCIPAL_INVESTIGATOR
Hartford Hosptial Division of Urogynecology

Study Locations (Sites)

Hartford Hospital
Hartford, Connecticut, 06106
United States

Collaborators and Investigators

Sponsor: Hartford Hospital

  • Nicole J Wood, MD, PRINCIPAL_INVESTIGATOR, Hartford Hosptial Division of Urogynecology
  • Elena Tuntisky-Bitton, MD, PRINCIPAL_INVESTIGATOR, Hartford Hosptial Division of Urogynecology

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-07-22
Study Completion Date2025-04-01

Study Record Updates

Study Start Date2024-07-22
Study Completion Date2025-04-01

Terms related to this study

Keywords Provided by Researchers

  • Artificial Intelligence

Additional Relevant MeSH Terms

  • Uterovaginal Prolapse
  • Urinary Incontinence
  • Lower Urinary Tract Symptoms