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Heart Failure, SystolicADHERE-HFNCT05988749

Digital Remote Home Monitoring for Heart Failure

A study testing Biofourmis Digital Platform in people with Heart Failure, Systolic, run by University of Texas Southwestern Medical Center at 2 sites in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

We will enroll 150 adult participants with systolic heart failure into the ADHERE-HF trial. The study will randomize participants in a 1:2 fashion to usual care or usual care plus the American Heart Association's Digital Solution for 90 days. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Heart Failure, Systolic
What is being tested?
Biofourmis Digital Platform
Could I receive a placebo?
No, everyone receives an active treatment
How many people
15 participants
Where
2 sitesUnited States
Study dates
13 Dec 2024to 30 Nov 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • ≥18-year-old adults with a clinical diagnosis of heart failure AND a left ventricular ejection fraction ≤40% by transthoracic echocardiogram or cardiac MRI within 12 months prior to enrollment.

Who cannot join

  • Patients who are pregnant.
  • Patients who do not have a smartphone or access to the Internet
  • Prisoners or refugees.
  • Patients who are homeless or have unstable housing.
  • Unable or unwilling to consent or use study related materials.
  • On-going cocaine, methamphetamine, opioid, alcohol, or other illicit substance abuse as determined by the study PI.
Show all 13Show fewer
  • Not fluent in English or Spanish.
  • Students or trainees at UT-Southwestern or Parkland Health System.
  • Enrolled or considering hospice.
  • Recent or home inotropic therapy, or heart transplant evaluation.
  • Survival anticipated <6 months.
  • End-stage renal disease, receiving dialysis or eGFR ≤30 mL/min/1.73m2
  • Non-Texas resident

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • Parkland Health & Hospital System

    Dallas, Texas, 75235

  • UT Southwestern Medical Center

    Dallas, Texas, 75390

Other trials in United States

About this study

Official title: American Heart Association Digital Home Remote Monitoring for Heart Failure

We will enroll 150 adult participants with systolic heart failure into the ADHERE-HF trial. The study will randomize participants in a 1:2 fashion to usual care or usual care plus the American Heart Association's Digital Solution for 90 days. This wearable device and careplan package is hypothesized to improve rates of guideline directed heart failure medical care for participants.

Read the detailed description

Background/Rationale:

Guideline-directed medical therapy (GDMT) is a cornerstone of the management of individuals with heart failure with reduced ejection fraction (HFrEF). Patients on optimal heart failure pharmacotherapy experience higher survival rates and fewer heart failure hospitalizations compared with subjects not on these medications [1,2]. Furthermore, optimal compliance with these treatments among patients with heart failure is associated with fewer have fewer emergency department visits, fewer hospital admissions, shorter lengths of hospital stay, and lower risk of death [3,4].

Despite very strong evidence for these treatments, a substantial proportion of eligible subjects with HFrEF are not on GDMT at optimal dosages. Data from the CHAMP-HF registry demonstrate that fewer than one in four HFrEF subjects are on all three of GDMT medications - beta-blockers; angiotensin-converting enzyme inhibitor (ACEi)/angiotensin II receptor blocker (ARB), or angiotensin receptor neprilysin inhibitor (ARNI); and mineralocorticoid receptor antagonist (MRA) - and only 1% were receiving target doses of all three medications [4]. Published data for both UT-Southwestern and Parkland Health System have demonstrated that rates of GDMT are above national averages but remain suboptimal with significant room for improvement.

Successful interventions to increase the number of subjects of prescribed GDMT at optimal doses often have included multidisciplinary heart failure clinics that include advanced practice providers and/or pharmacists with frequent visits [5,6]. However, such strategies are resource-intensive and are not widely applicable to heart failure management outside of specialized heart failure clinics. Health systems, such as Parkland Health System and UT-Southwestern, have also considered and purchased remote home monitoring programs for patients with systolic heart failure to try to improve prescription rates of GDMT. However, few studies have evaluated the impact of remote home monitoring on rates of GDMT in highly diverse patient populations or patients with increased socioeconomic risk.

As such, there is a crucial unmet need to implement highly effective GDMT titration strategies in heart failure populations with increased socioeconomic risk and the effects of remote monitoring systems to improve GDMT are not well known.

To address this gap in knowledge, we will leverage the large, multiethnic heart failure populations followed in two health systems, UT-Southwestern and Parkland Health System. Using these racially and ethnically diverse patient populations, we will test our central hypothesis that the AHA Digital Platform will improve outcomes in patients with HFrEF by managing the initiation and titration of heart failure GDMT in comparison with clinical care. The purpose of this study is to assess the effectiveness of the remote monitoring AHA Digital Platform to improve initiation and titration of GDMT in addition to traditional clinical encounters. The effective comparison will be to the current standard of care for heart failure used in the respective clinical sites.

The AHA Digital platform integrates data from remote wireless vital signs collection devices and an investigational wearable health device to recommend optimal titration of GDMT in subjects with heart failure with reduced ejection fraction (HFrEF) subjects or HFrEF subjects on suboptimal doses of GDMT. The platform uses a proprietary algorithm to interpret the remote vitals data collected and presents titration recommendations back to the healthcare provider (HCP) via a HCP mobile App for subjects randomized to the Intervention Arm at his/her site. Vitals data and relevant HF educational materials are simultaneously presented to the subject via a Patient App. Data from an investigational wearable health device is also provided to both the HCP and subject, however no care decisions are made with the data from this device. The HCP is also alerted to changes in status of the respective participating trial subjects via the HCP App and can see aggregated information and further visualize the status of all subjects enrolled in his/her center via an online web portal.

Hypothesis We hypothesize that use of the AHA Digital Solution in a real-world, multi-site, randomized, outpatient study will improve rates and does of optimal Guideline-Directed Medical Therapy (GDMT) for patients with heart failure with reduced ejection fraction.

Being tested
Biofourmis Digital Platform
Keywords
remote home monitoring, heart failure, guideline directed medical therapy
Medical subject headings
Heart Failure, Systolic, Heart Failure

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Biofourmis Digital PlatformOther

    Also called American Heart Association's Digital Heart Failure CarePlans and Education Content

    The intervention is a combination of the American Heart Association's Digital Heart Failure CarePlans and Education Content, delivered through and combined with the Biofourmis Platform. Patients enrolled in this arm will wear the device for 90 days and provide data to the participant's care team.

Study groups in NCT05988749
Study groupRoleWhat they receive
DeviceExperimentalParticipants will receive usual care or usual care plus the American Heart Association's Digital Solution in patients with HFrEF. The Solution is a combination of the AHA/CHTI HF CarePlans and Education Content, delivered through and combined with the Biofourmis Platform.
Receives: Other: Biofourmis Digital Platform
Routine CareNo interventionRoutine care for heart failure management

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. GDMT score

    Change in GDMT score from between the intervention and control arm.

    Measured: 0-90 days

Secondary outcomes (6)
  1. Hospitalized days

    Number of days hospitalized between the intervention and control arm

    Measured: 0-90 days; 0-180 days

  2. Emergency room visits

    Number of emergency room visits between the intervention and control arm

    Measured: 0-90 days; 0-180 days

  3. GDMT score

    Change in GDMT score from between the intervention and control arm.

    Measured: 0-180 days

  4. Change in KCCQ-12 score

    Change in overall and subdomain KCCQ-12 scores from between the intervention and control arm

    Measured: day 0-90 and 0-180

  5. Visual analog score change

    Change in visual analog scores from between the intervention and control arm

    Measured: day 0-90

  6. Optimal GDMT dosing

    Difference between the intervention and control arm in the percentage of subjects on optimal doses of GDMT

    Measured: 0-90 days, 0-180 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Aug 2023
  2. Study start13 Dec 2024
  3. Primary completion30 Nov 2025
  4. Study completion30 Nov 2025

Why it stopped: Due to sponsor request for poor enrollment

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Single group
Model description
Patients will be randomized in a 1:2 fashion to usual care versus usual care plus the American Heart Association's Digital Solution by dice roll.
Masking
None (open label)
Enrolment
15 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05988749
Sponsor's protocol ID
STU-2023-0529
Acronym
ADHERE-HF
Status last verified
Feb 2026
First submitted
4 Aug 2023
Last updated
18 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Biofourmis Digital Platform in people with Heart Failure, Systolic, run by University of Texas Southwestern Medical Center at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 18 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Due to sponsor request for poor enrollment). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

GDMT score (time frame: 0-90 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Feb 2026.

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