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Continuum: Digital Health to Manage Heart Failure Outpatients

Primary Purpose

Heart Failure, Chronic Heart Failure

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Continuum HFC-IN
Standard of care for the follow-up
Continuum HFC-OUT
Sponsored by
Centre hospitalier de l'Université de Montréal (CHUM)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Heart Failure focused on measuring Digital health, Digital therapeutics, Software as medical device, Remote patient management, Telemonitoring, Mobile health, Guideline-Directed Medical Therapy

Eligibility Criteria

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

HFC-IN

Inclusion Criteria:

  • HF diagnostic
  • NYHA 2 or +
  • Active follow-up in heart failure clinic
  • Ability to use mobile app (or with caregiver's help)
  • And one of the following
  • New HF diagnosis (<3 months)
  • Emergency visit or recent hospitalization with decompensated HF (<6months)
  • Increase of >50% diuretic dose, new diuretic or IV diuretic (last 3 months)
  • Active heart failure follow-up 2 times in the last 3 months

HFC-OUT

Inclusion Criteria:

  • HF diagnostic
  • Ability to use mobile app (or with caregiver's help)
  • No active follow-up in heart failure clinic or in the waiting list of one

Exclusion Criteria for HFC-IN and HFC-OUT:

  • Active hospitalization at randomization or anticipated in the next 2 weeks
  • Incapable or minor patient
  • History of non-adherence or treatment refusal
  • Alcohol or drugs abuse
  • Active major depression without caregiver
  • Global prognosis < 3months
  • Active dialysis or on waiting list
  • Heart transplant or mechanical heart
  • Severe pulmonary disease with oxygen use or pulmonary transplant waiting list or recurrent pleural drainage
  • Severe chronic cirrhosis or hepatic transplant waiting list or recurrent ascites drainage
  • Percutaneous or surgical intervention in last 30 days or planned in next 3 months
  • Pregnancy
  • Active follow-up in another study

Sites / Locations

  • CRCHUM

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Arm Label

For patients followed in a heart failure clinic (HFC), intervention HFC-IN

For patients followed in a HFC, control HFC-IN

For patients not followed in a HFC, intervention HFC-OUT

For patients not followed in a HFC, control HFC-OUT

Arm Description

Use of the full Continuum solution: remote patient monitoring and digital therapeutics over a period of 12 weeks

Standard of care for the follow-up, no use of remote monitoring or digital therapeutics for the first 12 weeks. After 12 weeks, option is given to the patient to use the full Continuum solution for another period of 12 weeks.

Use of part of the Continuum solution: the patient will use a mobile application to enter her/his data but no remote monitoring is performed. Digital therapeutics are used for the healthcare professionals.

Standard of care for the follow-up, no use of a mobile application or digital therapeutics for the first 12 weeks. After 12 weeks, option is given to the patient to use the mobile app and digital therapeutics are activated for another period of 12 weeks.

Outcomes

Primary Outcome Measures

CLIC IN ONLY: care consumption
Cost analysis on number of hospital (planned or unplanned) ambulatory visits, emergency visits, consultations and hospitalizations
CLIC OUT ONLY: Change in guideline-directed medical therapy by classes
Change in guideline-directed medical Therapy optimization between groups before and after intervention by medication classes.
CLIC OUT ONLY: Change in guideline-directed medical therapy by dose
Change in guideline-Directed Medical Therapy optimization between groups before and after intervention by medication doses.

Secondary Outcome Measures

CLIC OUT ONLY: Care consumption
Cost analysis on number of hospital (planned or unplanned) ambulatory visits, emergency visits, consultations and hospitalizations during intervention
CLIC IN ONLY: Change in guideline-directed medical therapy by classes
Compare guideline-Directed Medical Therapy optimization between groups before and after intervention by medication classes
CLIC IN ONLY: Change in guideline-directed medical therapy by doses
Compare guideline-Directed Medical Therapy optimization between groups before and after intervention by medication doses
MACE and other clinical events
Differences before-after between groups in number of main clinical events including unplanned appointments, emergency consults, all-cause or heart-failure hospitalizations, deaths
CLIC IN ONLY: Quality of life assessment (QoL) with the Kansas City Cardiomyopathy Questionnaire
Differences in score before and after
Quality of life assessment (QoL) with the EQ-5D-5L EuroQOL instrument
Differences in score before and after
New York Heart Association class
A reduction of at least one class in New York Heart Association (NYHA) scale
NTproBNP
Reduction in NTproBNP greater than 30%
Pharmacological profile
Percentage of recommended heart failure drugs prescribed

Full Information

First Posted
May 5, 2022
Last Updated
April 12, 2023
Sponsor
Centre hospitalier de l'Université de Montréal (CHUM)
Collaborators
Greybox, Boehringer Ingelheim
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1. Study Identification

Unique Protocol Identification Number
NCT05377190
Brief Title
Continuum: Digital Health to Manage Heart Failure Outpatients
Official Title
Continuum: Digital Health as Part of the Care Trajectory of Heart Failure Outpatients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 8, 2022 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
June 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre hospitalier de l'Université de Montréal (CHUM)
Collaborators
Greybox, Boehringer Ingelheim

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Heart failure (HF) is one of the leading causes of hospitalization and death worldwide. Remote patient monitoring and digital therapeutics could help reduce the consumption of care for these patients (hospitalizations, emergency room visits) and optimize their management (education, medication optimization). This randomized study aims to evaluate the effects of the Continuum software solution in patients with heart failure, whether or not they are followed in specialized clinics. Heart failure is one of the main causes of hospitalization and death in the world. Evidence suggests that remote patient monitoring (RPM) and digital therapeutics (DTX solutions) can help improve care consumption (i.e. hospitalizations, emergency visits) and also support health care professionals to improve care (i.e. symptoms management, drug optimization). This randomised study aims to evaluate the effects of these two software solutions in the context of specialized HF clinics (HFC) and primary health care on health care consumption and clinical events.
Detailed Description
According to Canadian recommendations, patients recently diagnosed with heart failure or with a recent hospitalization should have a medical follow-up every two to four weeks in order to optimize their treatment and quickly stabilize their condition. However, despite a network of specialized heart failure clinics in the province of Quebec, access to this service is still a challenge because of limited human resources and unequal geographic distribution. Only the most severely ill and unstable patients are followed in these clinics. The Continuum project combines a remote patient monitoring solution with therapeutic interventions driven by a software to manage heart failure (also called digital therapeutics (DTx)). The patient can send her/his clinical data to the healthcare professional using a mobile application. Healthcare professionals receive not only these data in realtime with potential alerts but also a summarized report of these data and suggested therapeutic interventions. Our hypotheses are that the Continuum solution, by combining RPM and DTx will 1) improve the workflow and the care trajectory of patients in heart failure clinics resulting in a reduction of cost per patient followed and 2) accelerate drug optimization so they can fully benefit from the recommended therapies for their specific condition. The general objective of this project is to assess in outpatients the effectiveness of the Continuum solution to reduce healthcare costs and to support medication optimization over a period of 12 weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Chronic Heart Failure
Keywords
Digital health, Digital therapeutics, Software as medical device, Remote patient management, Telemonitoring, Mobile health, Guideline-Directed Medical Therapy

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
For patients followed in a heart failure clinic (HFC), intervention HFC-IN
Arm Type
Experimental
Arm Description
Use of the full Continuum solution: remote patient monitoring and digital therapeutics over a period of 12 weeks
Arm Title
For patients followed in a HFC, control HFC-IN
Arm Type
Placebo Comparator
Arm Description
Standard of care for the follow-up, no use of remote monitoring or digital therapeutics for the first 12 weeks. After 12 weeks, option is given to the patient to use the full Continuum solution for another period of 12 weeks.
Arm Title
For patients not followed in a HFC, intervention HFC-OUT
Arm Type
Experimental
Arm Description
Use of part of the Continuum solution: the patient will use a mobile application to enter her/his data but no remote monitoring is performed. Digital therapeutics are used for the healthcare professionals.
Arm Title
For patients not followed in a HFC, control HFC-OUT
Arm Type
Placebo Comparator
Arm Description
Standard of care for the follow-up, no use of a mobile application or digital therapeutics for the first 12 weeks. After 12 weeks, option is given to the patient to use the mobile app and digital therapeutics are activated for another period of 12 weeks.
Intervention Type
Other
Intervention Name(s)
Continuum HFC-IN
Intervention Description
Combination of a mobile application (with remote monitoring) and digital therapeutics
Intervention Type
Other
Intervention Name(s)
Standard of care for the follow-up
Intervention Description
No mobile application or digital therapeutics are used
Intervention Type
Other
Intervention Name(s)
Continuum HFC-OUT
Intervention Description
Combination of a mobile application (without remote monitoring) and digital therapeutics
Primary Outcome Measure Information:
Title
CLIC IN ONLY: care consumption
Description
Cost analysis on number of hospital (planned or unplanned) ambulatory visits, emergency visits, consultations and hospitalizations
Time Frame
12 weeks
Title
CLIC OUT ONLY: Change in guideline-directed medical therapy by classes
Description
Change in guideline-directed medical Therapy optimization between groups before and after intervention by medication classes.
Time Frame
12 weeks
Title
CLIC OUT ONLY: Change in guideline-directed medical therapy by dose
Description
Change in guideline-Directed Medical Therapy optimization between groups before and after intervention by medication doses.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
CLIC OUT ONLY: Care consumption
Description
Cost analysis on number of hospital (planned or unplanned) ambulatory visits, emergency visits, consultations and hospitalizations during intervention
Time Frame
12 weeks
Title
CLIC IN ONLY: Change in guideline-directed medical therapy by classes
Description
Compare guideline-Directed Medical Therapy optimization between groups before and after intervention by medication classes
Time Frame
12 weeks
Title
CLIC IN ONLY: Change in guideline-directed medical therapy by doses
Description
Compare guideline-Directed Medical Therapy optimization between groups before and after intervention by medication doses
Time Frame
12 weeks
Title
MACE and other clinical events
Description
Differences before-after between groups in number of main clinical events including unplanned appointments, emergency consults, all-cause or heart-failure hospitalizations, deaths
Time Frame
12 weeks
Title
CLIC IN ONLY: Quality of life assessment (QoL) with the Kansas City Cardiomyopathy Questionnaire
Description
Differences in score before and after
Time Frame
12 weeks
Title
Quality of life assessment (QoL) with the EQ-5D-5L EuroQOL instrument
Description
Differences in score before and after
Time Frame
12 weeks
Title
New York Heart Association class
Description
A reduction of at least one class in New York Heart Association (NYHA) scale
Time Frame
12 weeks
Title
NTproBNP
Description
Reduction in NTproBNP greater than 30%
Time Frame
12 weeks
Title
Pharmacological profile
Description
Percentage of recommended heart failure drugs prescribed
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
HFC-IN Inclusion Criteria: HF diagnostic NYHA 2 or + Active follow-up in heart failure clinic Ability to use mobile app (or with caregiver's help) And one of the following New HF diagnosis (<3 months) Emergency visit or recent hospitalization with decompensated HF (<6months) Increase of >50% diuretic dose, new diuretic or IV diuretic (last 3 months) Active heart failure follow-up 2 times in the last 3 months HFC-OUT Inclusion Criteria: HF diagnostic Ability to use mobile app (or with caregiver's help) No active follow-up in heart failure clinic or in the waiting list of one Exclusion Criteria for HFC-IN and HFC-OUT: Active hospitalization at randomization or anticipated in the next 2 weeks Incapable or minor patient History of non-adherence or treatment refusal Alcohol or drugs abuse Active major depression without caregiver Global prognosis < 3months Active dialysis or on waiting list Heart transplant or mechanical heart Severe pulmonary disease with oxygen use or pulmonary transplant waiting list or recurrent pleural drainage Severe chronic cirrhosis or hepatic transplant waiting list or recurrent ascites drainage Percutaneous or surgical intervention in last 30 days or planned in next 3 months Pregnancy Active follow-up in another study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
François Tournoux, MD PhD
Organizational Affiliation
CHUM
Official's Role
Principal Investigator
Facility Information:
Facility Name
CRCHUM
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H2X 0A9
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Continuum: Digital Health to Manage Heart Failure Outpatients

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