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NCT Number: NCT07503054

Ovarian Cancer Screening and AI

Gynecologists frequently overestimate the benefits and safety of ovarian cancer screening. AI-supported discussions may help correct these misperceptions. This study tests whether an AI-guided conversation about the evidence on ovarian cancer screening can improve gynecologists' knowledge and reduce non-evidence-based screening recommendations, compared with a control AI discussion on ovarian cancer prevalence.

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Key information

Age range

24 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Charité - Universitätsmedizin Berlin

Mitte, State of Berlin, 10117, Germany

About this study

Previous research has demonstrated that gynecologists often substantially overestimate both the effectiveness and safety of ovarian cancer screening, despite robust evidence indicating that such screening does not offer a net clinical benefit. These findings highlight the need for innovative communication strategies to support evidence-based clinical practice and reduce low value care.

AI-based conversational interventions have shown promising results in other fields when aiming to correct misconceptions or encourage engagement with evidence, particularly among individuals who are initially resistant to factual information. Leveraging these insights, this study investigates whether AI-facilitated discussions can effectively improve gynecologists' knowledge of the benefit-harm profile of ovarian cancer screening and subsequently reduce non-evidence-based recommendations.

The study employs a cross-sectional study design in which gynecologists who have previously indicated to regularly recommend ovarian cancer screening with transvaginal ultrasound and potentially with additional CA 125-testing to their asymptomatic, average-risk patients are randomized to one of two conditions:

  • Intervention Condition: Participants engage in an AI-guided conversation in which they explain their reasons for recommending ovarian cancer screening. The AI is instructed to address misconceptions and clarify the lack of evidence supporting a positive benefit-harm ratio.
  • Control Condition: Participants engage in an AI discussion on the prevalence of ovarian cancer, without receiving information or corrective feedback related to screening outcomes.

Before and after the AI-based discussion, all participants are queried on their numerical (X out of 1,000 women) and subjective perception of ovarian cancer screening's benefits and harms and their screening recommendations. Measures are derived from instruments used in prior research.

The primary objective of this study is to assess the change, from before to after the AI-based conversation, in clinicians' understanding of the benefit-harm ratio and their recommendations regarding routine ovarian cancer screening for asymptomatic, average-risk women, within and between study groups.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • gynecologists in outpatient care who provide ovarian cancer screening to asymptomatic, average-risk women (not guideline consistent)

Exclusion criteria

  • gynecologists in inpatient care
  • gynecologist in outpatient care who do NOT provide ovarian cancer screening to asymptomatic, average-risk women (guideline consistent)

Treatment and study plan

ChatGPT - Control

Behavioral

Three-turn conversation; discusses ovarian cancer risk and epidemiology; avoids screening topics; concise responses (5-8 sentences).

Mode of Delivery: Online chat interface; participant interacts directly with ChatGPT.

ChatGPT - Evidence-Based Screening Discussion

Behavioral

Three-turn conversation; asks participants about screening rationale; provides evidence-based info on benefits/harms, trial data, guideline positions; concise responses (5-8 sentences).

Mode of Delivery: Online chat interface; participant interacts directly with ChatGPT.

Primary outcomes

  1. Change in intention to recommend ovarian cancer screening

    Time frame: Immediately post intervention

    Difference in participants' self-reported frequency of recommending ovarian cancer screening to average-risk women in the future after the ChatGPT interaction and their self-reported frequency of recommending the screening in the past.

Secondary outcomes

  1. Change in benefit-harm ratio evaluation of ovarian cancer screenings

    Time frame: Immediately post intervention

    Difference between the self-reported benefit-harm ratio evaluation before and after the ChatGPT interaction.

  2. Accuracy of knowledge regarding ovarian cancer screening evidence

    Time frame: Immediately post intervention

    Participants' understanding of benefits, harms, and guideline recommendations for ovarian cancer screening, assessed via survey questions

Study contacts

Contact information is provided by the study sponsor or research team.

Miriam K Rumpel, M.Sc.

CONTACT

[email protected]

+49 30 450 531 058

Odette Wegwarth, Prof. Dr.

CONTACT

[email protected]

+49 30 450 531 074

Sponsors and collaborators

Lead sponsor

Charite University, Berlin, Germany

Other

Collaborators

  • German Research Foundation
  • Max Planck Institute for Human Development

Registry information

Official study title

AI on Ovarian Cancer Screening Attitudes in Gynecologists

Acronym: AI-OCS-Gyn

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 31, 2026
Registry last updated
Mar 31, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.