- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07829640
AI-Assisted Chest CT Interpretation Across the Lung Cancer Care Continuum
Development of a Chest CT-Based Artificial Intelligence Model Across the Lung Cancer Care Continuum and a Prospective Randomized Crossover Reader Study of Its Clinical Decision-Support Performance
This investigator-initiated, single-center study consists of a retrospective artificial intelligence model-development stage and a prospective physician reader-study stage. Deidentified chest CT examinations acquired during routine clinical care between January 1, 2021, and December 31, 2024, will be used to develop, validate, and lock artificial intelligence models for lung cancer-related imaging tasks.
In the prospective stage, approximately 12 to 15 physicians with experience in chest CT interpretation will complete two reading sessions in randomized order: unaided interpretation and AI-assisted interpretation. The sessions will be separated by a washout period of at least 4 weeks. The primary objective is to compare diagnostic performance between AI-assisted and unaided interpretation. Secondary objectives include reading time, diagnostic confidence, inter-reader agreement, and errors related to incorrect AI suggestions.
All readings will be performed in an offline research environment. AI outputs will not be used for patient care, and the study will not add imaging examinations, treatment, or follow-up for patients.
연구 개요
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Lian Yang, PhD
- 전화번호: +86 18986273791
- 이메일: yanglian@hust.edu.cn
연구 장소
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Hubei
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Wuhan, Hubei, 중국, 430022
- Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
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연락하다:
- Lian Yang, PhD
- 전화번호: +86 18986273791
- 이메일: yanglian@hust.edu.cn
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-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Physicians with education or training relevant to medical imaging
- Experience in interpreting chest CT examinations
- Ability to complete the required study training and both reading sessions
- Willingness to provide written informed consent and comply with study procedures
Exclusion Criteria:
- Failure to complete the required study training
- Inability or unwillingness to complete both reading sessions as required
- Any protocol deviation likely to compromise the validity of the reader-study data
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 특수 증상
- 할당: 무작위
- 중재 모델: 크로스오버 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Sequence AB: Unaided Then AI-Assisted Interpretation
Participants first complete an unaided chest CT interpretation session. After a washout period of at least 4 weeks, they complete an AI-assisted interpretation session. |
A locked research-use-only artificial intelligence system analyzes deidentified chest CT images and provides decision-support outputs to participating physicians. The system is evaluated only in an offline reader-study environment and is not used for actual patient care. |
|
실험적: Sequence BA: AI-Assisted Then Unaided Interpretation
Participants first complete an AI-assisted chest CT interpretation session. After a washout period of at least 4 weeks, they complete an unaided interpretation session. |
A locked research-use-only artificial intelligence system analyzes deidentified chest CT images and provides decision-support outputs to participating physicians. The system is evaluated only in an offline reader-study environment and is not used for actual patient care. |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Difference in Diagnostic Accuracy Between AI-Assisted and Unaided Chest CT Interpretation
기간: At completion of the second reading session, after a washout period of at least 4 weeks
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Diagnostic accuracy will be calculated as the proportion of case-level interpretations that agree with the prespecified reference standard based on pathology or clinical follow-up. The paired difference in diagnostic accuracy between AI-assisted and unaided interpretation will be estimated across participating physicians and cases using a multi-reader multi-case analysis and reported with a 95% confidence interval. Higher accuracy indicates better diagnostic performance. |
At completion of the second reading session, after a washout period of at least 4 weeks
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .