search
Back to results

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

Primary Purpose

Heart Failure

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Telemonitoring
Conventional care
Sponsored by
University Hospital, Grenoble
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Heart Failure focused on measuring Heart failure, Telemonitoring, therapeutic education, care network, hospitalization

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Private Geriatric Hospital Magnolias
  • Hospital Group Mutualiste
  • University Hospital of Grenoble

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Telemonitoring

Conventional care

Arm Description

Home-based patient management using AUTONOM@DOM telemonitoring system to record and transmit heart rate, blood pressure and weight; along side conventional care (patient therapeutic education or personalised care program)

Conventional care including patient therapeutic education or personalised care program

Outcomes

Primary Outcome Measures

Hospitalization
Hospitalization 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 Outcome Measures

Comparison of quality of life
loss of autonomy and loss of function, quality of life, depression and anxiety, malnutrition, mortality and clinical stage of the disease
medicoeconomic criteria
health expenditures and quality of life first. If follow-up turns out feasible, cost-effectiveness and cost-utility ratios
efficacy telemonitoring system criteria
number and type of telemonitoring alerts and their clinical relevance

Full Information

First Posted
April 9, 2014
Last Updated
May 24, 2018
Sponsor
University Hospital, Grenoble
Collaborators
Medico-economic evaluation unit , University Hospital, Grenoble
search

1. Study Identification

Unique Protocol Identification Number
NCT02135458
Brief Title
Evaluation of the AUTONOM@DOM Telemonitoring System for People With Heart Failure
Acronym
AUTONOM@DOM
Official Title
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.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
April 2014 (Actual)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
June 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Grenoble
Collaborators
Medico-economic evaluation unit , University Hospital, Grenoble

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
Heart failure, Telemonitoring, therapeutic education, care network, hospitalization

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
84 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Telemonitoring
Arm Type
Experimental
Arm Description
Home-based patient management using AUTONOM@DOM telemonitoring system to record and transmit heart rate, blood pressure and weight; along side conventional care (patient therapeutic education or personalised care program)
Arm Title
Conventional care
Arm Type
Active Comparator
Arm Description
Conventional care including patient therapeutic education or personalised care program
Intervention Type
Other
Intervention Name(s)
Telemonitoring
Intervention Type
Other
Intervention Name(s)
Conventional care
Other Intervention Name(s)
Patient therapeutic education: ETICS HPGM, or, Personalized care program: RESIC 38
Primary Outcome Measure Information:
Title
Hospitalization
Description
Hospitalization 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.
Time Frame
one year
Secondary Outcome Measure Information:
Title
Comparison of quality of life
Description
loss of autonomy and loss of function, quality of life, depression and anxiety, malnutrition, mortality and clinical stage of the disease
Time Frame
one year
Title
medicoeconomic criteria
Description
health expenditures and quality of life first. If follow-up turns out feasible, cost-effectiveness and cost-utility ratios
Time Frame
one year
Title
efficacy telemonitoring system criteria
Description
number and type of telemonitoring alerts and their clinical relevance
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Muriel SALVAT, MD
Organizational Affiliation
University Hospital, Grenoble
Official's Role
Principal Investigator
Facility Information:
Facility Name
Private Geriatric Hospital Magnolias
City
Ballainvilliers
ZIP/Postal Code
91160
Country
France
Facility Name
Hospital Group Mutualiste
City
Grenoble
ZIP/Postal Code
38028
Country
France
Facility Name
University Hospital of Grenoble
City
Grenoble
ZIP/Postal Code
38043
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
23999456
Citation
Maggioni AP, Greene SJ, Fonarow GC, Bohm M, Zannad F, Solomon SD, Lewis EF, Baschiera F, Hua TA, Gimpelewicz CR, Lesogor A, Gheorghiade M; ASTRONAUT Investigators and Coordinators. Effect of aliskiren on post-discharge outcomes among diabetic and non-diabetic patients hospitalized for heart failure: insights from the ASTRONAUT trial. Eur Heart J. 2013 Oct;34(40):3117-27. doi: 10.1093/eurheartj/eht342. Epub 2013 Sep 2.
Results Reference
background
PubMed Identifier
23478743
Citation
Gheorghiade M, Bohm M, Greene SJ, Fonarow GC, Lewis EF, Zannad F, Solomon SD, Baschiera F, Botha J, Hua TA, Gimpelewicz CR, Jaumont X, Lesogor A, Maggioni AP; ASTRONAUT Investigators and Coordinators. Effect of aliskiren on postdischarge mortality and heart failure readmissions among patients hospitalized for heart failure: the ASTRONAUT randomized trial. JAMA. 2013 Mar 20;309(11):1125-35. doi: 10.1001/jama.2013.1954. Erratum In: JAMA. 2013 Apr 10;309(14):1461.
Results Reference
background
PubMed Identifier
23186936
Citation
Logeart D, Isnard R, Resche-Rigon M, Seronde MF, de Groote P, Jondeau G, Galinier M, Mulak G, Donal E, Delahaye F, Juilliere Y, Damy T, Jourdain P, Bauer F, Eicher JC, Neuder Y, Trochu JN; Heart Failure of the French Society of Cardiology. Current aspects of the spectrum of acute heart failure syndromes in a real-life setting: the OFICA study. Eur J Heart Fail. 2013 Apr;15(4):465-76. doi: 10.1093/eurjhf/hfs189. Epub 2012 Nov 27.
Results Reference
background
PubMed Identifier
21634217
Citation
Jourdain P, Juilliere Y; Steering and Working Group Committee Members of the French Task Force on Therapeutic Education in Heart Failure. Therapeutic education in patients with chronic heart failure: proposal for a multiprofessional structured programme, by a French Task Force under the auspices of the French Society of Cardiology. Arch Cardiovasc Dis. 2011 Mar;104(3):189-201. doi: 10.1016/j.acvd.2010.12.003. No abstract available.
Results Reference
background
PubMed Identifier
21127322
Citation
Roncalli J, Mouquet F, Piot C, Trochu JN, Le Corvoisier P, Neuder Y, Le Tourneau T, Agostini D, Gaxotte V, Sportouch C, Galinier M, Crochet D, Teiger E, Richard MJ, Polge AS, Beregi JP, Manrique A, Carrie D, Susen S, Klein B, Parini A, Lamirault G, Croisille P, Rouard H, Bourin P, Nguyen JM, Delasalle B, Vanzetto G, Van Belle E, Lemarchand P. Intracoronary autologous mononucleated bone marrow cell infusion for acute myocardial infarction: results of the randomized multicenter BONAMI trial. Eur Heart J. 2011 Jul;32(14):1748-57. doi: 10.1093/eurheartj/ehq455. Epub 2010 Dec 2.
Results Reference
background
PubMed Identifier
19717851
Citation
Jondeau G, Neuder Y, Eicher JC, Jourdain P, Fauveau E, Galinier M, Jegou A, Bauer F, Trochu JN, Bouzamondo A, Tanguy ML, Lechat P; B-CONVINCED Investigators. B-CONVINCED: Beta-blocker CONtinuation Vs. INterruption in patients with Congestive heart failure hospitalizED for a decompensation episode. Eur Heart J. 2009 Sep;30(18):2186-92. doi: 10.1093/eurheartj/ehp323. Epub 2009 Aug 30.
Results Reference
background

Learn more about this trial

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

We'll reach out to this number within 24 hrs