New Taipei City 888 Digital Medical AI Platform for Prevention and Care of the Three Highs and Cardio-Renal-Vascular Diseases

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorNew Taipei City Medical Association

About this trial

Non-communicable diseases (NCDs), or chronic diseases, are a major public health burden globally and in Taiwan, and control of the "three highs" (hypertension, dyslipidemia, and hyperglycemia) is a national priority. Nearly half of the 10 leading causes of death in Taiwan are directly or indirectly related to atherosclerotic cardiovascular disease (ASCVD), for which hypertension, dyslipidemia, and abnormal blood glucose are the major risk factors. National health insurance data indicate that over 70% of middle-aged and older adults have at least one of these chronic conditions. Early stages are often asymptomatic, and inadequate control may lead to complications of cardiovascular disease, stroke, renal vascular disease, and retinopathy, causing irreversible organ damage and death.

For blood pressure, large clinical trials such as SPRINT and STEP have shown that targeting systolic blood pressure below 130 mmHg significantly reduces ASCVD events. For LDL cholesterol, "the lower, the better" applies, with guideline-recommended LDL-C targets determined by baseline ASCVD risk, with levels below 55 mg/dL for very high-risk patients. For diabetes, treatment goals generally include fasting plasma glucose below 130 mg/dL and glycated hemoglobin (HbA1c) below 7%.

Although antihypertensive therapy has been proven effective in preventing cardiovascular disease and chronic kidney disease attributable to hypertension, fewer than one-third of patients receiving antihypertensive medications achieve current guideline-recommended blood pressure targets. No randomized clinical trial to date has used home blood pressure as the primary therapeutic reference. Moreover, long-term evidence is lacking regarding the organ-protective effects of strategies targeting morning hypertension and of bedtime dosing regimens. Although the TIME study is currently the largest and longest-followed trial addressing dosing time, its bedtime-dosing arm was not specifically targeted to patients with morning hypertension. Therefore, we propose a clinical trial to investigate management strategies for morning hypertension. Aligned with the 2022 Taiwan Hypertension Guidelines, we will employ the "722 protocol" for home blood pressure monitoring and enroll patients with morning home blood pressure ≥130/80 mmHg to compare selective nocturnal administration of antihypertensive agents versus exclusive morning dosing, assessing differences in morning home blood pressure control rates, end-organ damage, and atherosclerotic cardiovascular disease (ASCVD) events.

This project will implement two large-scale cluster-randomized clinical trials within the New Taipei City healthcare network. The first trial (T-888-DIGICARE) will evaluate whether a mobile digital health platform augmented with interactive digital modules can more effectively achieve the "888" targets for prevention and treatment of the Three Highs (Hypertension, Hyperglycemia, Hyperlipidemia). The second trial (DREAM-G) will use the same mobile health delivery model to investigate whether the timing of antihypertensive medication administration (nocturnal versus morning dosing) differentially affects patients with poor morning home blood pressure control. Beyond generating rigorous evidence through a novel clinical approach, this program is expected to have substantial global clinical impact and to showcase Taiwan's healthcare capabilities internationally. Operational challenges encountered and solutions developed during the trials will also provide critical feasibility data for the concurrent real-world implementation registry (T-888-DIGICARE-Registry). The registry will run in parallel with the cluster trials and will enroll individuals who decline trial participation at baseline as well as participants after trial completion, thereby serving as a continuity and real-world evidence platform.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Hypertension

Office blood pressure: two consecutive measurements >130/80 mmHg

Home blood pressure: weekly average (morning/evening) >130/80 mmHg, or more than half of the weekly measurements exceeding this threshold

Hyperlipidemia

Disqualifiers

Symptomatic heart failure (New York Heart Association functional class II-IV)

End-stage renal disease requiring long-term dialysis

Pregnant women or those planning pregnancy

Life expectancy <1 year

Trial design

Design model

Parallel

Treatments tested in this trial

  • Interactive digital modules

    Behavioral

    Whether the Mobile Digital Health Platform augmented with interactive digital modules improves control rates of the Three Highs (Hypertension, Hyperglycemia, Hyperlipidemia), target organ damages and cardiovascular outcomes

  • Antihypertensive Medication Management

    Behavioral

    Therapeutic effects of selective nocturnal versus universal morning antihypertensive dosing on morning home blood pressure control and target organ damages

Treatment groups

4,162 Participants
are divided into 4 treatment groups
Group A: Standard careNo intervention 0 interventions
Group B: bedtime dosingExperimental treatment 1 intervention
Group C: Conventional morning dosingNo intervention 0 interventions
Group D: Degital careExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Mean home blood pressure <130/80 mmHg.

T-888-DIGICARE study

Time frame
24 months from baseline
2

LDL-C <100 mg/dL (and <70 mg/dL for patients with diabetes or ASCVD).

T-888-DIGICARE study

Time frame
24 months from baseline
3

HbA1c <6.5% or a reduction of at least 1% from baseline if baseline HbA1c >8% or at least 2% if baseline HbA1c >10%.

T-888-DIGICARE study

Time frame
24 months from base line
4

≥30% reduction in urine albumin to creatinine ratio (UACR).

T-888-DIGICARE study

Time frame
24 months from baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

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New Taipei City Medical Association

Lead sponsor

National Taiwan University

Collaborator