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Recruiting NCT06525181

NCT06525181 AI as an Aid for Weekly Symptom Intake in Radiotherapy

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Clinical Trial Summary
NCT ID NCT06525181
Status Recruiting
Phase
Sponsor jaide
Condition Radiotherapy Side Effect
Study Type INTERVENTIONAL
Enrollment 200 participants
Start Date 2024-07-22
Primary Completion 2024-11-01

Trial Parameters

Condition Radiotherapy Side Effect
Sponsor jaide
Study Type INTERVENTIONAL
Phase N/A
Enrollment 200
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-07-22
Completion 2024-11-01
Interventions
Generative Artificial IntelligenceStandard weekly symptom intake

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Brief Summary

The study investigates the use of artificial intelligence (AI) and large language models (LLMs) to enhance the efficiency and accuracy of weekly treatment consultations (OTVs) in radiotherapy. It hypothesizes that an AI-enabled symptom summary tool will match traditional medical review methods in accuracy while saving time. The study includes patients undergoing pelvic radiotherapy and excludes those with pelvic reirradiation or who have undergone surgery. Patients will receive both standard and AI-assisted weekly consultations, with AI summaries generated using the OpenAI GPT-4 API. Blinded oncologists will compare the accuracy and quality of the AI-generated and doctor-generated summaries, while patients and doctors will rate these summaries. The primary objective is to evaluate the accuracy and time efficiency of AI-assisted symptom summaries compared to traditional methods.

Eligibility Criteria

Inclusion Criteria: All patients undergoing radiotherapy in the pelvic region. Exclusion Criteria: Cases of pelvic reirradiation or operated cases.

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