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Remote Monitoring of Chronic Heart Failure in Veneto Region

Primary Purpose

Congestive Heart Failure

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Telemonitoring for patients with Congestive Heart Failure
Sponsored by
Regione Veneto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Congestive Heart Failure focused on measuring CHF, Telemonitoring

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥ 65 years.
  • Discharge from hospital after acute heart failure in the previous 3 months and EF < 40% or EF > 40% plus BNP > 400 (or plus NT-proBNP>1500) during hospitalization

Exclusion Criteria:

  • Comorbidities prevalent on CHF with life expectation < 12 months.
  • Impossibility or inability to use the equipment and help at home not available.
  • Myocardial infarction or percutaneous coronary intervention in the last 3 months or scheduled.
  • Coronary artery bypass, valve substitution or correction in the last 6 months.
  • Being on waiting list for heart transplantation.
  • Being enrolled in other trial

Sites / Locations

  • Ospedale Immacolata Concezione - Cardiology Department
  • Presidio ospedaliero di Conegliano - Department of Cardiology
  • Ospedale di Mirano - Cardiology Department
  • Ospedale San Fracastoro - Cardiology Department
  • Azienda Ospedaliera di Padova - Cardiology Department
  • Ospedale Ca'Foncello - Pulmonology Department
  • Ospedale SS Giovanni e Paolo - Cardiology Department
  • Azienda Ospedaliera Universitaria Integrata di Verona - Geriatric Medicine Department

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control group

Telemonitoring for patients with Congestive Heart Failure

Arm Description

Treatment as usual

Outcomes

Primary Outcome Measures

Combined end point of all cause mortality and number of hospitalisations for heart failure

Secondary Outcome Measures

Cardiovascular and all-cause mortality
Health-Related Quality of Life
Health-Related Quality of Life is assessed by the SF-36 questionnaire
Number of hospitalisations (including rehospitalisations) for all causes and for heart failure
Total number of days in hospital
Number of specialist visits
Number of visits at emergency department for heart failure
Anxiety and depression status
Anxiety and depression status is assessed by Hospital Anxiety and Depression Scale (HADS)

Full Information

First Posted
January 17, 2012
Last Updated
October 27, 2015
Sponsor
Regione Veneto
Collaborators
European Commission, Azienda Unità Locale Socio Sanitaria n.9 Treviso, Azienda ULSS 7 Conegliano, Azienda ULSS 16 Padova, Azienda ULSS di Verona e Provincia, Azienda ULSS 12 Veneziana, Azienda Unità Socio Sanitaria di Dolo Mirano, Azienda Ospedaliera di Padova, Azienda Ospedaliera Universitaria Integrata Verona
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1. Study Identification

Unique Protocol Identification Number
NCT01513993
Brief Title
Remote Monitoring of Chronic Heart Failure in Veneto Region
Official Title
RENEWING HEALTH - Large Scale Pilot in Veneto Region: Remote Monitoring of Chronic Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
January 2012
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Regione Veneto
Collaborators
European Commission, Azienda Unità Locale Socio Sanitaria n.9 Treviso, Azienda ULSS 7 Conegliano, Azienda ULSS 16 Padova, Azienda ULSS di Verona e Provincia, Azienda ULSS 12 Veneziana, Azienda Unità Socio Sanitaria di Dolo Mirano, Azienda Ospedaliera di Padova, Azienda Ospedaliera Universitaria Integrata Verona

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate whether telemonitoring of patients with chronic heart failure produces a reduction in the combined end point of all cause mortality and number of hospitalisations, and whether it improves health related quality of life. In addition, the trials evaluate the economic and organisational impact of the telemonitoring service and examine its acceptability by patients and health professionals.
Detailed Description
The study is designed to evaluate the impact of telemonitoring on the management of CHF compared with outpatient usual care. From a clinical point of view, the trial will allow to investigate how telemonitoring contributes to reduct the combined end point of all cause mortality and re-hospitalizations, as well as the other kinds of access to hospital facilities (bed-days, specialistic and ER visits). The trial will examine whether the CHF patients improve their health-related quality of life and reduct the anxiety about health conditions, thanks to the telemonitoring. A cost-effectiveness and cost-utility analysis will be carried out in order to determine if and how telemonitoring helps to limit the healthcare expenditure. The evaluation will deal also with organizational changes and task shift due to telemonitoring introduction and patients and professional perception towards the service.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congestive Heart Failure
Keywords
CHF, Telemonitoring

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
315 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
No Intervention
Arm Description
Treatment as usual
Arm Title
Telemonitoring for patients with Congestive Heart Failure
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Telemonitoring for patients with Congestive Heart Failure
Intervention Description
Patients are equipped with a telemonitoring kit composed by a portable wrist-clinic device and digital weight scale for clinical parameters measuring and a gateway device for data transmission. The patient can monitor a complete set of clinical parameters, such as pulse-oxymetry, heart rate, blood pressure, ECG and body weight, with a frequency set by the clinician in the personalised treatment plan. Data are transmitted to a regional eHealth centre where a group of operators keeps these information under control and alerts the reference clinician in case of worsening of symptoms.
Primary Outcome Measure Information:
Title
Combined end point of all cause mortality and number of hospitalisations for heart failure
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Cardiovascular and all-cause mortality
Time Frame
12 months
Title
Health-Related Quality of Life
Description
Health-Related Quality of Life is assessed by the SF-36 questionnaire
Time Frame
12 months
Title
Number of hospitalisations (including rehospitalisations) for all causes and for heart failure
Time Frame
12 months
Title
Total number of days in hospital
Time Frame
12 months
Title
Number of specialist visits
Time Frame
12 months
Title
Number of visits at emergency department for heart failure
Time Frame
12 months
Title
Anxiety and depression status
Description
Anxiety and depression status is assessed by Hospital Anxiety and Depression Scale (HADS)
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 65 years. Discharge from hospital after acute heart failure in the previous 3 months and EF < 40% or EF > 40% plus BNP > 400 (or plus NT-proBNP>1500) during hospitalization Exclusion Criteria: Comorbidities prevalent on CHF with life expectation < 12 months. Impossibility or inability to use the equipment and help at home not available. Myocardial infarction or percutaneous coronary intervention in the last 3 months or scheduled. Coronary artery bypass, valve substitution or correction in the last 6 months. Being on waiting list for heart transplantation. Being enrolled in other trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zoran Olivari, DM
Organizational Affiliation
Azienda Unità Locale Socio Sanitaria n.9 Treviso
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ospedale Immacolata Concezione - Cardiology Department
City
Piove di Sacco
State/Province
Padova
ZIP/Postal Code
35028
Country
Italy
Facility Name
Presidio ospedaliero di Conegliano - Department of Cardiology
City
Conegliano
State/Province
Treviso
ZIP/Postal Code
31015
Country
Italy
Facility Name
Ospedale di Mirano - Cardiology Department
City
Mirano
State/Province
Venezia
ZIP/Postal Code
30035
Country
Italy
Facility Name
Ospedale San Fracastoro - Cardiology Department
City
San Bonifacio
State/Province
Verona
ZIP/Postal Code
37047
Country
Italy
Facility Name
Azienda Ospedaliera di Padova - Cardiology Department
City
Padova
ZIP/Postal Code
35128
Country
Italy
Facility Name
Ospedale Ca'Foncello - Pulmonology Department
City
Treviso
ZIP/Postal Code
31100
Country
Italy
Facility Name
Ospedale SS Giovanni e Paolo - Cardiology Department
City
Venezia
ZIP/Postal Code
30122
Country
Italy
Facility Name
Azienda Ospedaliera Universitaria Integrata di Verona - Geriatric Medicine Department
City
Verona
ZIP/Postal Code
37124
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
19687005
Citation
Scherr D, Kastner P, Kollmann A, Hallas A, Auer J, Krappinger H, Schuchlenz H, Stark G, Grander W, Jakl G, Schreier G, Fruhwald FM; MOBITEL Investigators. Effect of home-based telemonitoring using mobile phone technology on the outcome of heart failure patients after an episode of acute decompensation: randomized controlled trial. J Med Internet Res. 2009 Aug 17;11(3):e34. doi: 10.2196/jmir.1252.
Results Reference
background
PubMed Identifier
17426062
Citation
Clark RA, Inglis SC, McAlister FA, Cleland JG, Stewart S. Telemonitoring or structured telephone support programmes for patients with chronic heart failure: systematic review and meta-analysis. BMJ. 2007 May 5;334(7600):942. doi: 10.1136/bmj.39156.536968.55. Epub 2007 Apr 10.
Results Reference
background
PubMed Identifier
21733889
Citation
Inglis SC, Clark RA, McAlister FA, Stewart S, Cleland JG. Which components of heart failure programmes are effective? A systematic review and meta-analysis of the outcomes of structured telephone support or telemonitoring as the primary component of chronic heart failure management in 8323 patients: Abridged Cochrane Review. Eur J Heart Fail. 2011 Sep;13(9):1028-40. doi: 10.1093/eurjhf/hfr039. Epub 2011 Jul 6.
Results Reference
background
PubMed Identifier
21080835
Citation
Chaudhry SI, Mattera JA, Curtis JP, Spertus JA, Herrin J, Lin Z, Phillips CO, Hodshon BV, Cooper LS, Krumholz HM. Telemonitoring in patients with heart failure. N Engl J Med. 2010 Dec 9;363(24):2301-9. doi: 10.1056/NEJMoa1010029. Epub 2010 Nov 16. Erratum In: N Engl J Med. 2011 Feb 3;364(5):490. N Engl J Med. 2013 Nov 7;369(19):1869.
Results Reference
background
PubMed Identifier
19850208
Citation
Klersy C, De Silvestri A, Gabutti G, Regoli F, Auricchio A. A meta-analysis of remote monitoring of heart failure patients. J Am Coll Cardiol. 2009 Oct 27;54(18):1683-94. doi: 10.1016/j.jacc.2009.08.017. Erratum In: J Am Coll Cardiol. 2010 May 11;55(19):2185.
Results Reference
background
PubMed Identifier
20687083
Citation
Inglis SC, Clark RA, McAlister FA, Ball J, Lewinter C, Cullington D, Stewart S, Cleland JG. Structured telephone support or telemonitoring programmes for patients with chronic heart failure. Cochrane Database Syst Rev. 2010 Aug 4;(8):CD007228. doi: 10.1002/14651858.CD007228.pub2.
Results Reference
background
Links:
URL
http://www.renewinghealth.eu
Description
The Renewing Health project is partially funded under the ICT Policy Support Programme (ICT PSP) as part of the Competitiveness and Innovation Framework Programme by the European Community

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Remote Monitoring of Chronic Heart Failure in Veneto Region

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