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A Study of the Personal Health Record Application for Self-Management of Hypertension Detected at Health Screening

An Exploratory Study of the Personal Health Record Application for Self-Management of Hypertension Detected at Health Screening - Ex-SMART trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1040250109
Enrollment
70
Registered
2025-10-07
Start date
2025-10-07
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension Hypertension, Heart failure

Interventions

self-management through a dedicated smartphone app

Sponsors

Dohi Kaoru
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age 18 years or older 2. Blood pressure measured at physical examination or in the examination room: SBP140-179 and/or DBP90-109 mmHg 3. SBP 130 mmHg or higher as measured by ABPM 4. Ownership of a smartphone that can be connected to the Internet environment and on which this application can be installed 5. The patient's free and voluntary written consent to participate in this study has been obtained after sufficient informed consent

Exclusion criteria

Exclusion criteria: 1. Those who do not have access to an Internet environment or do not have a smartphone capable of installing this application 2. Those who are unable to use a smartphone due to cognitive or physical decline or disability 3. Those who have withdrawn their consent to the installation of this application, the terms of use, and the consent form. 4. Those whose inclusion in the study is deemed inappropriate by the principal investigator or co-investigator 5. Those who are participating in other clinical studies that may affect the treatment of hypertension, or who are scheduled to participate in this study while participating in this study. 6. Patients with marked hypertension (equivalent to degree III hypertension) or those in need of emergency antihypertensive treatment.

Design outcomes

Primary

MeasureTime frame
Mean change in systolic blood pressure (SBP) at 24-hour ambulatory blood pressure monitoring (ABPM) at 12 weeks

Secondary

MeasureTime frame
Mean change in ABPM diastolic blood pressure (DBP), percentage achieving -5 mmHg systolic and diastolic respectively, change in home blood pressure, change in office blood pressure, change in quality of life (QOL), app use/medication adherence rate, change in urinary sodium/potassium ratio

Contacts

Public ContactIto Hiromasa

Mie University Hospital

h-ito@med.mie-u.ac.jp+81-59-231-5015

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026