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Digital Health Intervention

Telemonitoring for Heart Failure (Medly-AID Trial)

N/A
Waitlist Available
Led By Emily Seto, PhD
Research Sponsored by University Health Network, Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Adults (18 years or older)
Hospitalization for decompensated HF > 48 hours
Must not have
Terminal diagnosis of any health condition with a life expectancy < 1 year
Patients who will require inpatient rehabilitation after discharge
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 month, 3 months
Awards & highlights
No Placebo-Only Group

Summary

This trial will test a new smartphone app, Medly, for patients recently diagnosed with heart failure. The app is designed to help manage self-care and improve quality of life. The trial will measure if the app leads to a reduction in 30-day readmissions rates, without increasing the average length of stay or visits to the emergency department.

Who is the study for?
This trial is for adults over 18 who've been hospitalized for heart failure longer than 48 hours. They must speak and read English (or have a caregiver who can translate) to use the Medly app, which monitors their condition after discharge. People with dementia, psychiatric illnesses, terminal conditions, or those in long-term care or other trials cannot join.
What is being tested?
The study tests if using the Medly telemonitoring system improves self-care and quality of life for heart failure patients post-discharge. It also checks if Medly reduces hospital readmissions within 30 days without increasing emergency visits or hospital stay lengths.
What are the potential side effects?
Since this trial involves monitoring through an app rather than medication, traditional side effects are not expected. However, there may be indirect effects related to stress from technology use or data privacy concerns.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 18 years old or older.
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I was hospitalized for heart failure symptoms for more than 48 hours.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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My doctor expects I have less than a year to live due to my condition.
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I will need inpatient rehab after I leave the hospital.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 month, 3 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 month, 3 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change BNP/NT-pro BNP levels
Change in NYHA class
Change in quality of life
+2 more
Secondary study objectives
30-day HF readmission rate
Hospital length of stay
Number of visits to the emergency department
Other study objectives
Safety Endpoint: Change in creatinine levels
Safety Endpoint: Change in potassium levels
Safety Endpoint: Change in sodium levels

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Telemonitoring (Medly)Experimental Treatment1 Intervention
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.
Group II: ControlActive Control1 Intervention
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.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Medly
2016
N/A
~100

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for heart failure include medications such as ACE inhibitors, beta-blockers, diuretics, and aldosterone antagonists. ACE inhibitors and beta-blockers work by reducing the workload on the heart and improving its efficiency, while diuretics help to remove excess fluid from the body, reducing symptoms like swelling and shortness of breath. Aldosterone antagonists help to prevent fluid retention and reduce the risk of hospitalization. Telemonitoring and positive behavior change, as studied in the Medly trial, enhance these treatments by enabling continuous monitoring of vital signs and promoting adherence to medication and lifestyle changes. This approach helps in early detection of worsening symptoms, timely intervention, and overall better management of heart failure, leading to improved quality of life and reduced hospital readmissions.

Find a Location

Who is running the clinical trial?

North York General HospitalOTHER
21 Previous Clinical Trials
8,734 Total Patients Enrolled
University Health Network, TorontoLead Sponsor
1,519 Previous Clinical Trials
503,082 Total Patients Enrolled
26 Trials studying Heart Failure
17,532 Patients Enrolled for Heart Failure
Sunnybrook Health Sciences CentreOTHER
674 Previous Clinical Trials
1,565,801 Total Patients Enrolled
5 Trials studying Heart Failure
46,664 Patients Enrolled for Heart Failure

Media Library

Telemonitoring (Digital Health Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT03358303 — N/A
Heart Failure Research Study Groups: Telemonitoring (Medly), Control
Heart Failure Clinical Trial 2023: Telemonitoring Highlights & Side Effects. Trial Name: NCT03358303 — N/A
Telemonitoring (Digital Health Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03358303 — N/A
~13 spots leftby Nov 2025