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The effect of tele-monitoring on post-cerebrovascular disoreder and cardiac disease patients at home care seeting

The effect of tele-monitoring on post-cerebrovascular disoreder and cardiac disease patients at home care seeting - The effect of tele-monitoring on post-cerebrovascular disoreder and cardiac disease patients at home care seeting

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000022783
Enrollment
20
Registered
2016-07-01
Start date
2016-06-14
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

hypertension, chronic hear disease, post-cerebrovascular diorder

Interventions

telemonitoring with vital sign sensor and sleep sensor without telemonitoring with vital sign sensor and sleep sensor

Sponsors

AMED
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients provided with regular visit by the physician at least twice every month 2) Patients at risk for any of the cerebral or cardiovascular diseases as below (1) Patients with previous or current history of hypertension (2) Patients with grade II, III or IV heart failure (New York Heart Association (NYHA) severity classification), BNP over 100 pg/mL or NT-proBNP over 400 pg/mL) (3) Patients with previous history of cerebral hemorrhage, cerebral infarction, or subarachnoid hemorrhage for more than 3 months prior to enrollment 3) Patients with written informed consent to participate obtained from subjects or representatives

Exclusion criteria

Exclusion criteria: 1) Patients with cancer. 2) Patients with a previous history of coronary artery disease, vascular disease, cerebral hemorrhage, cerebral infarction, or subarachnoid hemorrhage within 3 months prior to enrollment 3) Patients with a >=50% increase in serum creatinine within 3 months prior to enrollment 4) Patients on hormone replacement therapy with estrogen (estrogenic hormone products) 5) Patients who participated in another clinical study or clinical trial in the six months prior to enrollment 6) Patients judged inappropriate for this study by the physicians in charge

Design outcomes

Primary

MeasureTime frame
re-admittance due to exacerbation of heart failure, cerebrovascular disease and other cardiovascular events, and death within 9 months after intervention

Secondary

MeasureTime frame
NYHA grade BNP or NT-proBNP level cerebrovascular disease and other cardiovascular related medicine and its dose frequency of emergent doctor visit and doctor call blood pressure, pulse rate, respiratory rate satisfaction of patients, family and medical staff

Countries

Japan

Contacts

Public ContactShinsuke Muto

Tetsuyu Institute Medical Corporation President

shinsuke.muto@you-homeclinic.or.jp050-3784-2001

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026