- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07604129
Transcranial Sonography and Machine Learning for Schizophrenia Identification (TCS-ML-SZ)
Development and Validation of an Early Prediction Model for Schizophrenia Integrating Transcranial Sonography Structural Imaging and Machine Learning
Schizophrenia is a serious mental illness. Doctors usually diagnose schizophrenia by talking with patients, reviewing symptoms, and using clinical assessment. In early or less typical cases, diagnosis may be difficult.
This study will look at whether brain ultrasound information can help doctors identify features related to schizophrenia. The ultrasound scan used in this study is called transcranial sonography. It is a non-invasive scan that uses sound waves to look at brain structures through natural thin areas of the skull.
The study will include adults with schizophrenia and adults without a personal or family history of mental disorders. All participants will have a transcranial sonography scan and provide basic clinical information. The researchers will measure brain ultrasound features, including the substantia nigra, raphe nuclei, and third ventricle, and will combine these features with clinical information.
The main question is whether a computer model using ultrasound and clinical information can help distinguish adults with schizophrenia from adults without schizophrenia. The model is intended only as a research tool and possible future aid for doctors. It will not replace diagnosis by a psychiatrist and will not change the participant's usual medical care.
연구 개요
상세 설명
This is a prospective observational case-control study designed to develop and evaluate a machine-learning model for identifying schizophrenia using transcranial sonography (TCS) structural imaging features and clinical information.
Schizophrenia is clinically heterogeneous, and diagnosis depends mainly on clinical symptoms and psychiatric assessment. TCS is a non-invasive imaging method that can assess selected deep brain structures through the temporal acoustic window. Previous studies suggest that ultrasound features of structures such as the substantia nigra, raphe nuclei, and third ventricle may be related to neuropsychiatric disorders. This study will investigate whether TCS-derived structural imaging features, combined with clinical variables, can support auxiliary identification of schizophrenia.
Adults aged 18 to 65 years with schizophrenia diagnosed according to ICD-10 criteria and matched adults without a personal or family history of psychiatric disorders will be enrolled. The planned enrollment is 200 participants, including approximately 100 participants with schizophrenia and 100 healthy controls. Participants will undergo baseline TCS assessment and clinical data collection. No therapeutic intervention will be assigned by the investigators, and participation will not replace or alter usual clinical care.
TCS assessments will focus on selected brain structural imaging features, including substantia nigra echogenicity, raphe nuclei echogenicity, and third-ventricle width. Clinical information may include demographic characteristics, medical history, family history, disease course, medication history, and symptom assessment data when available. TCS measurements will be performed according to a standardized procedure, and image quality control will be conducted to reduce measurement variability.
The collected TCS and clinical variables will be integrated into a structured dataset for model development. Candidate machine-learning methods may include logistic regression, random forest, support vector machine, and XGBoost. Feature selection and model optimization will be performed within the model development process. Internal validation will be used to assess model performance, and additional independent data may be used for external validation if available.
Model performance will be evaluated using discrimination, calibration, and clinical utility metrics, including the area under the receiver operating characteristic curve, sensitivity, specificity, accuracy, F1 score, calibration assessment, and decision curve analysis where appropriate. Model interpretability will be explored using SHAP to assess the relative contribution of TCS imaging features and clinical variables.
The resulting model is intended as an auxiliary research tool for schizophrenia identification. It is not intended to make a definitive diagnosis, replace psychiatric assessment, or guide treatment decisions independently.
연구 유형
등록 (추정된)
연락처 및 위치
연구 연락처
- 이름: Xiaochen Zhang
- 전화번호: +8615967690053
- 이메일: 15967690053@163.com
연구 장소
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Zhejiang
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Taizhou, Zhejiang, 중국, 317200
- Taizhou Second People's Hospital
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연락하다:
- Xiaochen Zhang
- 전화번호: +8615967690053
- 이메일: 15967690053@163.com
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
Inclusion Criteria:
Schizophrenia group:
- Adults aged 18 to 65 years.
- Diagnosis of schizophrenia according to ICD-10 criteria by a psychiatrist.
- Able to complete clinical assessment and transcranial sonography examination.
- No other severe physical disease, neurological disease, or major psychiatric disorder.
- Written informed consent provided by the participant or legally authorized representative.
Healthy control group:
- Adults aged 18 to 65 years.
- No personal history of psychiatric disorders.
- No family history of psychiatric disorders.
- No severe physical disease, neurological disease, or major psychiatric disorder.
- Basic demographic characteristics matched as far as possible to the schizophrenia group.
- Able to complete clinical assessment and transcranial sonography examination.
- Written informed consent provided by the participant or legally authorized representative.
Exclusion Criteria:
- Severe physical disease or neurological disease.
- History of drug or alcohol abuse.
- Inability to complete clinical assessment or transcranial sonography examination.
- Inadequate temporal acoustic window or poor image quality preventing valid transcranial sonography measurements.
- Acute or clinically unstable state that prevents completion of study procedures.
- Comorbid major psychiatric disorder, such as major depressive disorder.
- Refusal or withdrawal of informed consent.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
개입 / 치료 |
|---|---|
|
Schizophrenia Group
Adults aged 18 to 65 years with schizophrenia diagnosed according to ICD-10 criteria.
Participants will undergo baseline transcranial sonography assessment and clinical data collection.
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Baseline transcranial sonography assessment of brain structural imaging features, including substantia nigra echogenicity, raphe nuclei echogenicity, and third-ventricle width.
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|
Healthy Control Group
Adults aged 18 to 65 years without a personal or family history of psychiatric disorders and matched as far as possible to the schizophrenia group by basic demographic characteristics.
Participants will undergo baseline transcranial sonography assessment and clinical data collection.
|
Baseline transcranial sonography assessment of brain structural imaging features, including substantia nigra echogenicity, raphe nuclei echogenicity, and third-ventricle width.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Area Under the ROC Curve of the Final TCS-Clinical Model
기간: Baseline; analyzed after completion of baseline data collection
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The area under the receiver operating characteristic curve will be used to assess the ability of the final machine-learning model, based on transcranial sonography and clinical variables, to distinguish participants with ICD-10 schizophrenia from healthy controls.
The reference standard will be clinical diagnosis according to ICD-10 criteria.
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Baseline; analyzed after completion of baseline data collection
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Sensitivity and Specificity of the Final TCS-Clinical Model
기간: Baseline; analyzed after completion of baseline data collection
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Sensitivity and specificity will be calculated for the final model for distinguishing participants with schizophrenia from healthy controls, using a pre-specified or internally optimized classification threshold.
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Baseline; analyzed after completion of baseline data collection
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Other Classification Performance Metrics of the Final Model
기간: Baseline; analyzed after completion of baseline data collection
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Accuracy, precision, recall, and F1 score will be calculated to further evaluate the classification performance of the final model for distinguishing participants with schizophrenia from healthy controls.
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Baseline; analyzed after completion of baseline data collection
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Calibration Performance of the Final TCS-Clinical Model
기간: Baseline; analyzed after completion of baseline data collection
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Calibration will be evaluated by comparing predicted probabilities with observed diagnostic status using calibration plots, calibration slope, calibration intercept, and/or Brier score, as appropriate.
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Baseline; analyzed after completion of baseline data collection
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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 연구와 관련된 용어
키워드
추가 관련 MeSH 약관
기타 연구 ID 번호
- 25YWB115
- TZEY-EC-2026-05 (기타 식별자: Ethics Committee of Taizhou Second People's Hospital)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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. .
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