CRITICALLY: Cardiovascular Risk Assessment and Dynamic Monitoring-based Prevention Trial

Sponsor
Peking University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05919056
Collaborator
Yinzhou District Center for Disease Control and Prevention (Other)
22,032
1
2
60.1
366.6

Study Details

Study Description

Brief Summary

The CRITICALLY study is a cluster randomized trial that will evaluate the effectiveness of a risk-based dynamic monitoring strategy for the primary prevention of cardiovascular high-risk Chinese adults.

Condition or Disease Intervention/Treatment Phase
  • Other: Frequent and automatic cardiovascular risk assessment
  • Other: Dynamic risk monitoring
  • Other: Regular GP visits
N/A

Detailed Description

The objective of the study is to evaluate the effectiveness of a risk-based management strategy on cardiovascular risk scores (calculated by the 2019 WHO cardiovascular risk charts) in 24 months (Phase I) and the incidence of major adverse cardiovascular events in 60 months (Phase II). Totally 216 clinics in Yinzhou District, China will be randomized to the intervention or the control arms with usual care. The interventions supported by the web-based decision support system include (1) cardiovascular risk assessment, (2) dynamic risk monitoring, and (3) regular visits by the general practitioner every three months. Only usual care will be provided in the control arm. The primary outcome is the change in cardiovascular risk scores for Phase I and the incidence of the composite endpoint of coronary heart disease, stroke, heart failure and all-cause mortality for Phase II. If the comprehensive strategy is proven effective, it could provide evidence for the primary prevention of cardiovascular diseases using digital health technology.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
22032 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Cardiovascular Risk Assessment and dynamIc Monitoring-based Prevention Trial for prImary Care quALity evaLuation in Yinzhou
Anticipated Study Start Date :
Jun 29, 2023
Anticipated Primary Completion Date :
Jul 1, 2028
Anticipated Study Completion Date :
Jul 1, 2028

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention arm

The interventions include cardiovascular risk assessment, dynamic risk monitoring, and regular general practitioner (GP) visits. The frequency of risk assessment, risk monitoring, and automatic mobile texting will be once per month, while regular GP visits will be once per three months.

Other: Frequent and automatic cardiovascular risk assessment
The 10-year cardiovascular risk scores using the 2019 World Health Organization (WHO) laboratory-based risk charts will be automatically calculated using the latest health information on an EHR-based system per month.

Other: Dynamic risk monitoring
High-risk individuals will be reassessed by the Dynamic Risk-based Early wArning and Monitoring (DREAM) system to obtain the short-term risk. The DREAM system will send a text message about advice to the high-risk individual every month. The text message includes information on the health status (e.g., current cardiovascular risk, level of blood pressure and lipid) and real-time warning messages (e.g., high short-term risk).

Other: Regular GP visits
The general practitioners will communicate with the participants based on the information automatically generated from the DREAM system every three months: each participant's cardiovascular risk score, health status (e.g., diabetes mellitus and/or hypertension), and Chinese guidelines-based recommendations (e.g., "for the management of dyslipidemia, to provide clear treatment targets for high-risk participants").

No Intervention: Control arm

Current regular management (usual care) will be kept in the control arm. The management objectives are for patients with hypertension or diabetes mellitus. The frequency of follow-up is at least once per three months.

Outcome Measures

Primary Outcome Measures

  1. Primary Outcome of Phase I: Change in cardiovascular risk score [24 months after baseline]

    The change in cardiovascular risk scores calculated by 2019 WHO laboratory-based risk charts

  2. Primary Outcome of Phase II: Major adverse cardiovascular events (MACE) [60 months after baseline]

    Incidence of coronary heart disease, stroke, heart failure and all-cause mortality

Secondary Outcome Measures

  1. Secondary Outcome of Phase I: Change in systolic blood pressure [24 months after baseline]

    the change in systolic blood pressure from baseline

  2. Secondary Outcome of Phase I: Change in total cholesterol [24 months after baseline]

    the change in total cholesterol from baseline

  3. Secondary Outcome of Phase I: Change in low-density lipoprotein cholesterol [24 months after baseline]

    the change in low-density lipoprotein cholesterol from baseline

  4. Secondary Outcome of Phase II: Change in health-related quality of life [60 months after baseline]

    Measured using the EuroQol-5 Dimensions-5L(EQ-5D)

Other Outcome Measures

  1. Other Pre-specified Outcome of Phase II: Incremental cost-effectiveness ratio (ICER) [60 months after baseline]

    the incremental cost-effectiveness ratio (ICER) of the management provided by the interventions compared to the usual care

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 79 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Residents in the Yinzhou District have a unique health ID;

  • Aged 40 to 79 years at the baseline enrollment;

  • With high risk of cardiovascular disease evaluated by the 2019 WHO laboratory-based risk models (10-year riskā‰„10%);

Exclusion Criteria:
  • Have a history of coronary heart disease, stroke or heart failure;

  • Patients with a diagnosis of cancer;

  • Refused to provide written informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Yinzhou District Center for Disease Control and Prevention Ningbo Zhejiang China 315100

Sponsors and Collaborators

  • Peking University
  • Yinzhou District Center for Disease Control and Prevention

Investigators

  • Principal Investigator: Xun TANG, PhD, MHS,
  • Principal Investigator: Pei GAO, PhD,

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Pei Gao, Professor, Peking University
ClinicalTrials.gov Identifier:
NCT05919056
Other Study ID Numbers:
  • IRB00001052-21060
First Posted:
Jun 26, 2023
Last Update Posted:
Jun 26, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Pei Gao, Professor, Peking University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 26, 2023