Data Driven Behavior Intervention and Medical Outcome Evaluation of Patients' Comprehensive Monitoring

NCT ID: NCT04966754

Last Updated: 2021-07-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-08-01

Study Completion Date

2023-11-30

Brief Summary

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During the study, the resuscitation room, general wards and ICU were installed fixed or mobile acquisition devices in the resuscitation room, the emergency department of Peking Union Medical College Hospital, and the collection platform was set up. Patients with acute diseases (infection, diabetes complications, etc.) caused by metabolic syndrome (obesity, diabetes, etc.) were selected after informed consent. All medical intervention behaviors, relevant medical records and medical outcome records within the collection scope of the device platform were collected prospectively . And regular follow-up, guidance of patients with metabolic syndrome control, while collecting all the lifestyle characteristics of patients, some patients with metabolic cabin research, and observe the relevant medical outcomes. After that, all the collected data were coded, and the influence of all lifestyle and medical behavior interventions on patients' medical outcomes was studied by artificial intelligence method.

Detailed Description

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Conditions

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Metabolic Syndrome Metabolic Disturbance Metabolic Complication Infection Obesity Diabetes

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Diabetes and / or obesity (BMI\>=28).
* Emergency room / emergency ward / EICU;
* Be able to understand and agree the research protocol and sign the informed consent

Exclusion Criteria

* Pregnant women / lactation period;
* The estimated survival time was less than 1 year;
* Long term follow-up is not guaranteed;
* Failure to comply with the protocol or procedure;
* The collection of medical behavior data can not complete the de privacy or label after de privacy;
* Other researchers think that it is not suitable for inclusion
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Peking University

OTHER

Sponsor Role collaborator

Guangdong Provincial People's Hospital

OTHER

Sponsor Role collaborator

Guangzhou Huyun Hospital Management Co., Ltd

UNKNOWN

Sponsor Role collaborator

Peking Union Medical College Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Central Contacts

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Huadong Zhu, MD

Role: CONTACT

13910696435 ext. 86

Wei Wang, Master

Role: CONTACT

15600994998

Provided Documents

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Document Type: Study Protocol

View Document

Other Identifiers

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JS-2898

Identifier Type: -

Identifier Source: org_study_id

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