Digital Health Platform Blood Pressure Management Study

Recruiting now · Not applicable

Conditions studied: Hypertension Prevention and Management

In brief

This pilot study evaluated the effectiveness of an AI health education assistant compared to case manager support in hypertension management. Key outcomes included changes in systolic blood pressure (SBP) and diastolic blood pressure (DBP), compliance with health behaviors, 722 goal achievement (monitoring, measurements, lifestyle improvements), and Technology Acceptance Model (TAM) metrics, including perceived usefulness (PU), perceived ease of use (PEU), and behavioral intention (BI). This study aims to examine whether the AI assistant group will achieve greater reductions in systolic and diastolic blood pressure compared to the case manager group. Additionally, it will evaluate whether the AI assistant group will demonstrate higher engagement in 722 goals and greater perceived ease of use. The results of this study are expected to provide further evidence supporting the potential of AI-driven interventions.

Key facts

Study ID

NCT07147413

Run by

Taipei Veterans General Hospital, Taiwan

People needed

1726

Starts

2025-09-01

Expected to finish

2027-12-31

Last updated by the study team

2026-07-15

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Participants must meet all of the following criteria:
• Aged 18 to 75 years at the time of enrollment
• Able and willing to provide informed consent
• Able to operate a mobile phone and interact with the digital platform
• Willing to participate in home blood pressure monitoring

You may not qualify if…

• Participants will be excluded if they meet any of the following criteria:
• Systolic BP consistently <120 mmHg and diastolic BP <70 mmHg, based on baseline home monitoring (considered low BP not targeted in this study)
• Pregnant or planning to become pregnant during the study period
• Unable to operate a smartphone or digital device independently
• Cognitive impairment or language barrier that prevents understanding of study procedures or informed consent
• Severe comorbidities that may interfere with study participation or outcomes (e.g., advanced heart failure, end-stage renal disease)
• Current participation in another interventional clinical study that could conflict with this protocol
• Unwillingness to follow home blood pressure monitoring protocol or adhere to follow-up schedule

Where it is running

• Taipei Veterans General Hospital — Taipei, Taiwan (enrolling)

Full record on ClinicalTrials.gov

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