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Implementation of SGLT-2 Inhibitors in Patients With Heart Failure Through a New Digital Strategy (EMAIL-HF)

Primary Purpose

Heart Failure

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Digital letter
Sponsored by
Morten Schou
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Heart Failure focused on measuring Heart Failure, SGLT-2 inhibitors, Digital implementation, Cardiorenal disease

Eligibility Criteria

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

Inclusion Criteria: Registered diagnosis of heart failure within the last 10 years Living in the Capital Region of Denmark or Roskilde Age ≥20 years Exclusion Criteria: Redeemed prescription of a SGLT-2 inhibitor after 2015 Type 1 diabetes History of diabetic ketoacidosis Chronic kidney disease in long term dialysis Living in a nursing home Dementia Cancer diagnosis within the last year (except prostate cancer and non-melanoma skin cancer) Exemption from the public digital mailbox system

Sites / Locations

  • Bispebjerg-Frederiksberg HospitalRecruiting
  • Herlev and Gentofte University HospitalRecruiting
  • Nordsjællands HospitalRecruiting
  • Amager-Hvidovre-Glostrup HospitalRecruiting
  • Sjællands Universitetshospital - RoskildeRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Digital letter

Control

Arm Description

The experimental group will receive a digital letter with information on the newly approved heart failure therapy option, SGLT-2 inhibitors. The letter will also invite recipients to be evaluated by a heart failure specialist for potential initiation of the therapy.

The control group will not be sent the digital letter and will therefore receive usual follow-up and care in the public healthcare system.

Outcomes

Primary Outcome Measures

Proportion of patients initiating therapy with a SGLT-2 inhibitor

Secondary Outcome Measures

Time to first occurrence of a composite heart failure endpoint consisting of all-cause death or heart failure hospitalisation.

Full Information

First Posted
May 3, 2023
Last Updated
June 30, 2023
Sponsor
Morten Schou
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1. Study Identification

Unique Protocol Identification Number
NCT05890131
Brief Title
Implementation of SGLT-2 Inhibitors in Patients With Heart Failure Through a New Digital Strategy
Acronym
EMAIL-HF
Official Title
Implementation of Sodium-Glucose Cotransporter (SGLT)-2 Inhibitors in Patients With Heart Failure Through a New Digital Strategy
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 3, 2023 (Actual)
Primary Completion Date
January 2025 (Anticipated)
Study Completion Date
January 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Morten Schou

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
The implementation of new medical therapies and guidelines, is a long and complex process that takes up to 10 years on average. This prolonged process is a global challenge and is mainly due to the complexity of cross-institutional patient care, involving primary care, out-patient clinics, nursing homes and patient associations. The main objective of this clinical trial is to determine whether a new digital strategy that employs official digital letters to inform and invite patients to evaluate their eligibility for new therapies, specifically the sodium-glucose co-transporter-2 (SGLT-2) inhibitor for heart failure patients, can facilitate and optimise the implementation. The aim is to increase the number of eligible patients with heart failure who start taking SGLT-2 inhibitors and reduce the time it takes to initiate treatment compared to the current process. Ultimately, this approach may improve patient outcomes.
Detailed Description
The study is a prospective, multicenter, two-armed, randomised clinical trial that will be coordinated from the Department of Cardiology, Herlev-Gentofte Hospital. The primary objective of the study is to determine whether a new digital strategy can be implemented to introduce novel medical therapies, specifically sodium-glucose co-transporter-2 (SGLT-2) inhibitors to heart failure patients. The aim is to increase the number of eligible patients who initiate therapy and to reduce the time taken to initiate therapy compared to the current process. The study will recruit patients with a registered diagnosis of heart failure residing in The Capital Region of Denmark and Roskilde, who have not yet been started on SGLT-2 inhibitor therapy. Patient identification and recruitment will be carried out through Danish nationwide registries, using their personal identification number (CPR-number), which is also linked to a secure digital mailbox where all official letters from public authorities are sent to Danish citizens. Patients will be randomly assigned (1:1) to receive a digital letter containing evidence-based information about the newly approved heart failure therapy option, SGLT-2 inhibitors. The letter will also invite recipients to be evaluated by a heart failure specialist for potential initiation of the therapy. Outcome measures will be obtained from Danish nationwide registers at pre-specified time points and in collaboration with the Danish Health Data Authority.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
Heart Failure, SGLT-2 inhibitors, Digital implementation, Cardiorenal disease

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
10000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Digital letter
Arm Type
Experimental
Arm Description
The experimental group will receive a digital letter with information on the newly approved heart failure therapy option, SGLT-2 inhibitors. The letter will also invite recipients to be evaluated by a heart failure specialist for potential initiation of the therapy.
Arm Title
Control
Arm Type
No Intervention
Arm Description
The control group will not be sent the digital letter and will therefore receive usual follow-up and care in the public healthcare system.
Intervention Type
Other
Intervention Name(s)
Digital letter
Intervention Description
A digital letter with evidence-based information about the newly approved heart failure therapy option, SGLT-2 inhibitors. The letter will also invite recipients to be evaluated by a heart failure specialist for potential initiation of the therapy.
Primary Outcome Measure Information:
Title
Proportion of patients initiating therapy with a SGLT-2 inhibitor
Time Frame
from randomisation up to 6 months
Secondary Outcome Measure Information:
Title
Time to first occurrence of a composite heart failure endpoint consisting of all-cause death or heart failure hospitalisation.
Time Frame
from randomisation up to 2 years
Other Pre-specified Outcome Measures:
Title
Number of all-cause deaths and heart failure hospitalisations
Time Frame
from randomisation up to 2 years
Title
Time to first occurrence of a 3-point expanded composite heart failure endpoint consisting of all-cause death, heart failure hospitalisation, or renal failure, with examination of the components of this composite.
Time Frame
from randomisation up to 2 years
Title
Time to first occurrence of a 4-point expanded composite heart failure endpoint consisting of all-cause death, heart failure hospitalisation, non-fatal myocardial infarction, non-fatal stroke, with examination of the components of this composite.
Time Frame
from randomisation up to 2 years
Title
Time to initiation of SGLT-2 inhibitor therapy
Time Frame
from randomisation up to 2 years
Title
Adherence to SGLT-2 inhibitor therapy (defined as proportion of days covered >=80%)
Time Frame
from randomisation up to 1 year
Title
Proportion of elderly (>75 years) initiating therapy with SGLT-2 inhibitors
Time Frame
from randomisation up to 2 years
Title
Proportion of patients with lower educational level initiating therapy with SGLT-2 inhibitors
Time Frame
from randomisation up to 2 years
Title
Proportion of patients with lower socioeconomic level initiating therapy with SGLT-2 inhibitors
Time Frame
from randomisation up to 2 years
Title
Proportion of immigrants initiating therapy with SGLT-2 inhibitors
Time Frame
from randomisation up to 2 years
Title
Proportion of patients with type 2 diabetes initiating therapy with SGLT-2 inhibitors
Time Frame
from randomisation up to 2 years
Title
Proportion of male and female patients initiating therapy with SGLT-2 inhibitors
Time Frame
from randomisation up to 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Registered diagnosis of heart failure within the last 10 years Living in the Capital Region of Denmark or Roskilde Age ≥20 years Exclusion Criteria: Redeemed prescription of a SGLT-2 inhibitor after 2015 Type 1 diabetes History of diabetic ketoacidosis Chronic kidney disease in long term dialysis Living in a nursing home Dementia Cancer diagnosis within the last year (except prostate cancer and non-melanoma skin cancer) Exemption from the public digital mailbox system
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Morten Schou, MD, PhD
Phone
0045 38683677
Email
morten.schou.04@regionh.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Mariam E Malik, MD
Email
mariam.elmegaard.malik@regionh.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Morten Schou, MD, PhD
Organizational Affiliation
Department of Cardiology, Herlev and Gentofte Hospital, 2900 Hellerup, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lars Køber, MD, DMSc
Organizational Affiliation
Department of Cardiology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark
Official's Role
Study Chair
Facility Information:
Facility Name
Bispebjerg-Frederiksberg Hospital
City
Copenhagen
ZIP/Postal Code
2400
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jens J Thune, MD, PhD
First Name & Middle Initial & Last Name & Degree
Jens J Thune, MD, PhD
First Name & Middle Initial & Last Name & Degree
Christian D Tuxen, MD, PhD
Facility Name
Herlev and Gentofte University Hospital
City
Hellerup
ZIP/Postal Code
2900
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Morten Schou, MD, PhD, Prof.
First Name & Middle Initial & Last Name & Degree
Morten Schou, MD, PhD, Prof.
First Name & Middle Initial & Last Name & Degree
Trine K Lauridsen, MD, PhD
Facility Name
Nordsjællands Hospital
City
Hillerød
ZIP/Postal Code
3400
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nis O Stride, MD, PhD
First Name & Middle Initial & Last Name & Degree
Nis O Stride, MD, PhD
First Name & Middle Initial & Last Name & Degree
Emil Wolsk, MD, PhD
Facility Name
Amager-Hvidovre-Glostrup Hospital
City
Hvidovre
ZIP/Postal Code
2650
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Morten Petersen, MD, PhD
First Name & Middle Initial & Last Name & Degree
Morten Petersen, MD, PhD
First Name & Middle Initial & Last Name & Degree
Anders Barasa, MD, PhD
First Name & Middle Initial & Last Name & Degree
Mads K Ersbøl, MD, PhD
Facility Name
Sjællands Universitetshospital - Roskilde
City
Roskilde
ZIP/Postal Code
4000
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nadia Dridi, MD, PhD
First Name & Middle Initial & Last Name & Degree
Nadia Dridi, MD, PhD
First Name & Middle Initial & Last Name & Degree
Lars Køber, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be collected from nationwide administrative registers, that are stored and managed by the Danish Health Data Authority. Data access can only be made available to a third party through an affiliation to an authorized Danish research environment. Please contact the sponsor-investigator in case of any inquiries.

Learn more about this trial

Implementation of SGLT-2 Inhibitors in Patients With Heart Failure Through a New Digital Strategy

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