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NCT07350486Active, not recruiting

LLM-CoManage: Large Language Model-Enabled Co-Management of Hypertension, Diabetes, and Dyslipidemia

A Cluster-Randomized Trial of Large Language Model-Enabled Coordinated Management for Hypertension, Diabetes, and Dyslipidemia in Community Settings (LLM-CoManage Trial)

Source: ClinicalTrials.gov · Last updated 4 Sept 2026

Brief summary (registry, in English)

This study aims to evaluate the effectiveness of a large language model (LLM)-supported, community-based integrated management model in improving cardiometabolic multimorbidity control among adults with hypertension and coexisting diabetes or dyslipidemia. Adopting an interventional study design, eligible patients will be recruited to compare the disease control indicators between LLM-assisted management and conventional management, so as to verify the effectiveness and safety of the former.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
6800 (estimated)
First submitted
25 Dec 2025
Start date
14 May 2026
Primary completion date
31 Mar 2027
Lead sponsor
First Hospital of China Medical University
NCT number
NCT07350486

What you commit to

  • Study type: Interventional
  • Planned participants: 6800
  • From 14 May 2026 to the primary completion date, 31 Mar 2027
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • Participating communities must meet all of the following criteria:
  • Have a designated community physician responsible for primary care who is capable of using a smartphone with stable internet access for clinical communication and LLM-assisted management;
  • No plan for administrative merger or restructuring within the next three years;
  • Located at least 2 kilometers away from adjacent participating communities (to minimize contamination between clusters).
    • Eligible participants must fulfill all of the following conditions:
  • Aged 40 years or older;
  • Uncontrolled hypertension, defined as systolic blood pressure (SBP) ≥140 mmHg or diastolic blood pressure (DBP) ≥ 90 mmHg;
  • Coexisting diabetes (HbA1c ≥ 7.0%) or coexisting dyslipidemia (LDL-C ≥ 3.4 mmol/L\[130 mg/dL\]);
  • Able to use a smartphone independently or with assistance from family members;
  • Has resided in the participating community for at least 6 months;
  • Has no plan to relocate in the next 3 years;
  • Enrolled in basic medical insurance for urban and rural residents, employee medical insurance, or the New Rural Cooperative Medical Scheme;
  • Not currently pregnant or planning pregnancy during the study period;
  • Free from malignant tumors and deemed to have a life expectancy of at least 3 years, as judged by study physicians;
  • Willing and able to provide written informed consent.

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cangzhou
Coordinator of this site? Confirm its status
CangzhouChinaUnknown status
Yiwu
Coordinator of this site? Confirm its status
JinzhouChinaUnknown status
Dawa District
Coordinator of this site? Confirm its status
PanjinChinaUnknown status
Shenyang
Coordinator of this site? Confirm its status
ShenyangChinaUnknown status
Wujiang District
Coordinator of this site? Confirm its status
SuzhouChinaUnknown status
Binhai New Area
Coordinator of this site? Confirm its status
TianjinChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.