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Effects of Telemonitoring on the Outcome of Heart Failure Patients After an Incidence of Acute Decompensation (Medly-AID)

Primary Purpose

Heart Failure

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Medly
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Heart Failure focused on measuring telemonitoring, smartphone application

Eligibility Criteria

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

Inclusion Criteria:

  • Adults (18 years or older)
  • Hospitalization for decompensated HF > 48 hours
  • Patient speaks and reads English adequately to provide informed consent and understand the text prompts in the application (or has an informal caregiver who can translate for them)
  • Ability to comply with using Medly (ex. able to stand on the weight scale, able to answer symptom questions, etc.)

Exclusion Criteria:

  • Dementia or uncontrolled psychiatric illness
  • Residents of long-term care facilities
  • Terminal diagnosis of any health condition with a life expectancy < 1 year
  • Patients who will require inpatient rehabilitation after discharge
  • Participating in another clinical trial that may confound the results

Sites / Locations

  • North York General Hospital
  • Sunnybrook Health Sciences Centre
  • Mount Sinai Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Telemonitoring (Medly)

Control

Arm Description

Medly is a smartphone application allows heart failure (HF) patients to measure and record their daily weight, blood pressure (BP), heart rate, and self-reported symptoms. This monitoring information is then transmitted wirelessly to a data server where an algorithm is used to generate an alert to a healthcare provider as necessary. The patient also receives an automated self-care message based on their measurements and reported symptoms.

Standard of care: Control groups will receive standard medical care when discharged from hospital, including discharge instructions, home medications as well as follow-up in a heart failure clinic or with a primary care doctor.

Outcomes

Primary Outcome Measures

Change in self-care of health failure
Change in self-care of health failure as measured by the Self-Care of Heart Failure Index (SCHFI)
Change in quality of life
Change in quality of life, as measured with the Kansas City Cardiomyopathy Questionnaire (KCCQ-12) and EuroQol (EQ5D)
Change BNP/NT-pro BNP levels
Change BNP/NT-pro BNP levels
Change in NYHA class
Change in NYHA class
Compliance with Medly utilization
Ability to adhere to Medly program

Secondary Outcome Measures

Hospital length of stay
Hospital length of stay
30-day HF readmission rate
30-day HF readmission rate
Number of visits to the emergency department
Number of visits to the emergency department

Full Information

First Posted
November 24, 2017
Last Updated
July 31, 2023
Sponsor
University Health Network, Toronto
Collaborators
Sunnybrook Health Sciences Centre, MOUNT SINAI HOSPITAL, North York General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03358303
Brief Title
Effects of Telemonitoring on the Outcome of Heart Failure Patients After an Incidence of Acute Decompensation
Acronym
Medly-AID
Official Title
Effect of a Mobile Phone-based Telemonitoring Program on the Outcome of Heart Failure Patients After an Incidence of Acute Decompensation
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 16, 2018 (Actual)
Primary Completion Date
November 30, 2023 (Anticipated)
Study Completion Date
November 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
Sunnybrook Health Sciences Centre, MOUNT SINAI HOSPITAL, North York General Hospital

4. Oversight

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

5. Study Description

Brief Summary
Heart failure is the most rapidly rising cardiovascular disease and has come to be recognized as a growing epidemic. Digital health interventions are the most recent iteration of an effort to promote individualized outpatient care through positive behaviour change theory. The UHN team has developed a highly automated and user-centered smartphone-based system, Medly, which allows for the telemonitoring of patients diagnosed with heart failure. The purpose of this study will be two-fold: 1) to determine if the introduction of Medly within two weeks of discharge will improve self-care management, quality of life, and clinical status, 2) to assess whether Medly will lead to a potential reduction in 30 day readmission rates amongst HF patients in the Toronto Central Local Health Integration Network (TC LHIN), without increasing the average length of stay or visits to the emergency department. These parameters will be measured as secondary outcomes.
Detailed Description
Heart failure is the most rapidly rising cardiovascular disease and has come to be recognized as a growing epidemic. Digital health interventions are the most recent iteration of an effort to promote individualized outpatient care through positive behaviour change theory. The UHN team has developed a highly automated and user-centered smartphone-based system, Medly, which allows for the telemonitoring of patients diagnosed with heart failure Patients with heart failure will be provided with a smartphone and commercial home medical devices, such as a blood pressure monitor and weight scale. The measurements from the medical devices will be automatically sent to the smartphone, and from there to a data server at the hospital for analysis and storage. Both clinicians and patients will be able to access these data and will be sent alerts by the system if the measurements are outside of the normal range. The system will be evaluated through interviews and comparing outcomes between the intervention and control groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
telemonitoring, smartphone application

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Telemonitoring (Medly)
Arm Type
Experimental
Arm Description
Medly is a smartphone application allows heart failure (HF) patients to measure and record their daily weight, blood pressure (BP), heart rate, and self-reported symptoms. This monitoring information is then transmitted wirelessly to a data server where an algorithm is used to generate an alert to a healthcare provider as necessary. The patient also receives an automated self-care message based on their measurements and reported symptoms.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Standard of care: Control groups will receive standard medical care when discharged from hospital, including discharge instructions, home medications as well as follow-up in a heart failure clinic or with a primary care doctor.
Intervention Type
Device
Intervention Name(s)
Medly
Intervention Description
Medly will enable patients with HF to take clinically relevant physiological measurements with wireless home medical devices and to answer symptom questions on the smartphone. The measurements will be automatically and wirelessly transmitted to the mobile phone and then to a data server. Automated self-care instructions/messages will be sent to the patient based on the readings and reported symptoms. If there are signs of their status deteriorating, an alert will be sent to a clinician that is responsible for the particular chronic condition of concern. The clinicians will have all the relevant patient data sent to them and will be able to access (through a secure web portal) to view historical and trending data for their patients.
Primary Outcome Measure Information:
Title
Change in self-care of health failure
Description
Change in self-care of health failure as measured by the Self-Care of Heart Failure Index (SCHFI)
Time Frame
Baseline, 3 months
Title
Change in quality of life
Description
Change in quality of life, as measured with the Kansas City Cardiomyopathy Questionnaire (KCCQ-12) and EuroQol (EQ5D)
Time Frame
Baseline, 3 months
Title
Change BNP/NT-pro BNP levels
Description
Change BNP/NT-pro BNP levels
Time Frame
Baseline, 2 weeks, 1 month, 3 months
Title
Change in NYHA class
Description
Change in NYHA class
Time Frame
Baseline, 3 months
Title
Compliance with Medly utilization
Description
Ability to adhere to Medly program
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Hospital length of stay
Description
Hospital length of stay
Time Frame
0 - 3 months
Title
30-day HF readmission rate
Description
30-day HF readmission rate
Time Frame
1 month
Title
Number of visits to the emergency department
Description
Number of visits to the emergency department
Time Frame
0 - 3 months
Other Pre-specified Outcome Measures:
Title
Safety Endpoint: Change in creatinine levels
Description
Change in creatinine levels
Time Frame
Baseline, 2 weeks, 1 month, 3 months
Title
Safety Endpoint: Change in sodium levels
Description
Change in sodium levels
Time Frame
Baseline, 2 weeks, 1 month, 3 months
Title
Safety Endpoint: Change in potassium levels
Description
Change in potassium levels
Time Frame
Baseline, 2 weeks, 1 month, 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults (18 years or older) Hospitalization for decompensated HF > 48 hours Patient speaks and reads English adequately to provide informed consent and understand the text prompts in the application (or has an informal caregiver who can translate for them) Ability to comply with using Medly (ex. able to stand on the weight scale, able to answer symptom questions, etc.) Exclusion Criteria: Dementia or uncontrolled psychiatric illness Residents of long-term care facilities Terminal diagnosis of any health condition with a life expectancy < 1 year Patients who will require inpatient rehabilitation after discharge Participating in another clinical trial that may confound the results
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emily Seto, PhD
Organizational Affiliation
University of Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
North York General Hospital
City
North York
State/Province
Ontario
ZIP/Postal Code
M2K 1E1
Country
Canada
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada
Facility Name
Mount Sinai Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X5
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30806625
Citation
Ware P, Dorai M, Ross HJ, Cafazzo JA, Laporte A, Boodoo C, Seto E. Patient Adherence to a Mobile Phone-Based Heart Failure Telemonitoring Program: A Longitudinal Mixed-Methods Study. JMIR Mhealth Uhealth. 2019 Feb 26;7(2):e13259. doi: 10.2196/13259.
Results Reference
background
PubMed Identifier
30064970
Citation
Ware P, Ross HJ, Cafazzo JA, Laporte A, Gordon K, Seto E. Evaluating the Implementation of a Mobile Phone-Based Telemonitoring Program: Longitudinal Study Guided by the Consolidated Framework for Implementation Research. JMIR Mhealth Uhealth. 2018 Jul 31;6(7):e10768. doi: 10.2196/10768.
Results Reference
background
PubMed Identifier
29724704
Citation
Ware P, Ross HJ, Cafazzo JA, Laporte A, Seto E. Implementation and Evaluation of a Smartphone-Based Telemonitoring Program for Patients With Heart Failure: Mixed-Methods Study Protocol. JMIR Res Protoc. 2018 May 3;7(5):e121. doi: 10.2196/resprot.9911.
Results Reference
background
PubMed Identifier
22356799
Citation
Seto E, Leonard KJ, Cafazzo JA, Barnsley J, Masino C, Ross HJ. Mobile phone-based telemonitoring for heart failure management: a randomized controlled trial. J Med Internet Res. 2012 Feb 16;14(1):e31. doi: 10.2196/jmir.1909.
Results Reference
background
PubMed Identifier
32012116
Citation
Seto E, Ross H, Tibbles A, Wong S, Ware P, Etchells E, Kobulnik J, Chibber T, Poon S. A Mobile Phone-Based Telemonitoring Program for Heart Failure Patients After an Incidence of Acute Decompensation (Medly-AID): Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2020 Jan 22;9(1):e15753. doi: 10.2196/15753.
Results Reference
derived

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Effects of Telemonitoring on the Outcome of Heart Failure Patients After an Incidence of Acute Decompensation

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