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Health in Smart Rurality: Impact on Coordination of Care of Telemonitoring and Data Centralization of Frailty Patients

Health in Smart Rurality: Impact on Coordination of Care of Telemonitoring and Data Centralization of Frailty Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04866550
Acronym
HIS2R
Enrollment
50
Registered
2021-04-29
Start date
2021-06-25
Completion date
2022-08-01
Last updated
2022-05-03

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

Conditions

Chronic Obstructive Pulmonary Disease, Heart Failure

Keywords

Chronic diseases, Aging people, Cross-border care, New communication technology

Brief summary

Chronic diseases are frequent (around 10% of the total population and 30% after 60 years) and accelerate age-related functional decline. Concerning cross-border patients, use of health services can be delayed given the distances, the lack of rapid road access and the limited availability of public transport and the complex organization of coordinated care. One of the ways to reduce acute exacerbations and preserve the quality of life of patients is to detect warning signs early. One of the ways to do this is to use new communication technologies.

Detailed description

The aim of the study is to assess feasibility of using a connected tablet to assess clinical parameters with an alert system in frailty patients aged over 60, living at home, with heart failure and / or chronic obstructive pulmonary disease, potentially requiring care cross-border (France and Belgium).

Interventions

OTHERData collection

Daily record of temperature, weight, heart rate, systolic blood pressure and oxygen saturation

Sponsors

Université de Reims Champagne-Ardenne
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged over 60 * Patients living at home * Patients with heart failure and / or chronic obstructive pulmonary disease, * Patients potentially requiring care cross-border (France and Belgium). * Patients agreeing to participate to the study

Exclusion criteria

* Patients who do not speak French * Patients with severe cognitive impairment

Design outcomes

Primary

MeasureTime frameDescription
Alert according to the connected tablet12 monthssignificant change in temperature (egal or more 38°), weight (variation of more than 5%), heart rate (less than 50 beats per minute or greater than 100), systolic blood pressure (less than 85 mmHg or greater than 160 mmHg) and / or oxygen saturation (variation of more than 4%)

Countries

France

Contacts

Primary ContactJean-Luc NOVELLA
jlnovella@chu-reims.fr03 26 78 44 10

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026