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NCT Number: NCT06961461

AI-assisted Quality Control Study of Multimodal Data in the Epidemiological Survey of Shanghai Nicheng Cohort Study

This study is based on the Nicheng Cohort study. This study intends to analyze whether AI assistance can effectively improve the efficiency and accuracy of quality control of data collected in large-scale epidemiological surveys based on traditional quality control processes.

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Key information

Sex eligibility

All sexes

Study type

Observational

About this study

This study randomly divided quality control personnel into an experimental group and a control group. The experimental group adopts AI assisted quality control: the AI system automatically transcribes the recorded text of the questionnaire, extracts keywords, analyzes the consistency of the Q&A logic, and generates quality control prompts. The quality control personnel will verify the question fragments according to the prompts and determine the qualification of the questionnaire; The control group relies entirely on manual quality control: the quality control personnel listen to the recording word by word, manually record the content, independently identify keyword omissions, logical contradictions, or terminology deviations, and ultimately determine whether the questionnaire is qualified. The core difference lies in the fact that the experimental group uses AI technology to accurately locate risk issues, reducing the burden of manual comprehensive screening, while the control group requires full manual review without targeted support.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Be proficient in using computers;
  • The person responsible for questionnaire quality control needs to have good dialect recognition ability;
  • Have a basic understanding or high acceptance of AI-assisted tools, and be able to adapt to the learning and application of new technologies
  • Be able to participate in the research throughout the process, abide by the research process, receive training, and be willing to complete quality control tasks as required.

Exclusion criteria

  • The person responsible for questionnaire quality control cannot understand or recognize Shanghai Nanhui dialect proficiently;
  • Unfamiliar with AI-assisted tools and difficult to accept technical operations;
  • Unable to participate in the research, receive training or complete the specified tasks due to other work or academic reasons;

Treatment and study plan

AI-assisted quality control tool

Other

In this study, quality control personnel will be randomly divided into an experimental group and a control group, and will use artificial intelligence-assisted quality control and manual quality control to conduct quality control on the data collected from the epidemiological survey.

Experimental group: Quality control personnel will use the AI system to perform quality control on the questionnaire recordings.

Control group: The questionnaire content was checked by manually listening back to the recordings and errors were recorded manually.

Primary outcomes

  1. Accuracy

    Time frame: From enrollment to the end of questionnaire quality control at 8 weeks

    changes in the efficiency and accuracy of quality control of data collected in large-scale epidemiological surveys with AI-assisted tool

Secondary outcomes

  1. Completeness and consistency

    Time frame: From enrollment to the end of questionnaire quality control at 8 weeks

    AI-assisted quality control in questionnaire quality control improves the integrity and consistency of questionnaire data through automated keyword extraction and logical consistency checking.

Sponsors and collaborators

Lead sponsor

Shanghai 6th People's Hospital

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
May 8, 2025
Registry last updated
May 8, 2025

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.

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