Skip to content

Evaluation of the AUTONOM@DOM Telemonitoring System for People With Heart Failure

Clinical and Medico-economic Assessment of Conventional Care Plus the Autonom@Dom Telemonitoring System Versus a Conventional Care Package Alone, for People With Heart Failure in Several French Structures.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02135458
Acronym
AUTONOM@DOM
Enrollment
84
Registered
2014-05-12
Start date
2014-04-30
Completion date
2017-06-30
Last updated
2018-05-25

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

Conditions

Heart Failure

Keywords

Heart failure, Telemonitoring, therapeutic education, care network, hospitalization

Brief summary

Heart failure is the principle cause of hospitalisation for people over 65. the assumption is that a system of home based telemonitoring can reduce the rate of unscheduled hospitalisation or rehospitalisation for heart failure (compared to a care package alone), This randomised controlled pilot study should assess the feasibility in terms of patient inclusion and follow-up.

Detailed description

Chronic diseases such as heart failure are a major burden for healthcare systems They are punctuated by exacerbations, often markers of poor prognosis, and are associated with expensive unscheduled hospitalizations. After initial diagnosis, despite the development of both drug and physical therapies, the rate of re-hospitalization for heart failure remains high with 50% or more of patients readmitted within 6 months. Recommendations for the treatment of heart failure patients are extremely precise and justify close collaboration between local community services and the hospital. However there is often considerable divergence between recommended care and the reality, due in particular to the difficulty in monitoring ambulatory patients. For example, the dose titration of beta-blockers or ACE inhibitors need to be monitored, and dosages of diuretics need to be adapted to avoid side effects which affect the quality of life of patients and limit medication adherence etc. The establishment of 'ambulatory' care networks (including multidisciplinary health professionnals of city and hospital and therapeutic patient education) such as that in Isère County in France has demonstrated its effectiveness. However, more advanced tools for patient monitoring still need to be assessed, particularly 'home monitoring', because there is not yet consensus as to the role tele-monitoring should play in the context of heart failure, and to date recommendations are vague. Assess the clinical and medico-economic benefit of an innovative patient monitoring strategy 'AUTONOM @ DOM' is needed. The primary aim of this study is then to assess a system of home based telemonitoring .The main outcome is unscheduled hospitalisation for heart failure. secondary aims were to assess the efficacy of this system, quality of life and medico-economic benefit. This pilot study is realised in the Isère and Essonne counties of France. Patients diagnosed with heart failure will be randomized to one of the following groups: * conventional care including at least a patient education program (ETICS program in Essone county and RESIC38 network in Isere county); * conventional care, plus home telemonitoring including a recording of the heart rate, blood pressure and weight, remotely transmitted to the cardiologist by an approved validated system that includes an alert monitoring feature. The study will last one year starting in April 2014.

Interventions

OTHERTelemonitoring
OTHERConventional care

Sponsors

Medico-economic evaluation unit , University Hospital, Grenoble
CollaboratorUNKNOWN
University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Age 60 years or more * Covered by French social security system or equivalent * Written informed consent signed by patient * Heart failure diagnosed by a cardiologue * NYHA stage II, III or IV * Able to be followed-up for 1 year * Attend general healthcare education sessions

Exclusion criteria

* Freedom restricted by judicial order * Under legal protection * Require peritoneal dialysis or hemofiltration * Participation refused by patient, primary care physician or cardiologist * Present a severe comorbidity with poor short-term prognosis * Present asymptomatic heart failure NYHA stage I * Programmed surgical intervention: valve prosthesis or revascularization * Impossibility to follow a program of patient education * Residing in medicalized care facility for persons without autonomy * Residing outside the recruitment zones

Design outcomes

Primary

MeasureTime frameDescription
Hospitalizationone yearHospitalization at any time during follow-up, emergency, unplanned, inappropriate or early (within one month) rehospitalization or not. The type and length of hospital stay will be recorded.

Secondary

MeasureTime frameDescription
Comparison of quality of lifeone yearloss of autonomy and loss of function, quality of life, depression and anxiety, malnutrition, mortality and clinical stage of the disease
medicoeconomic criteriaone yearhealth expenditures and quality of life first. If follow-up turns out feasible, cost-effectiveness and cost-utility ratios
efficacy telemonitoring system criteriaone yearnumber and type of telemonitoring alerts and their clinical relevance

Countries

France

Outcome results

None listed

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