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.
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.
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- 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
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.
- Conditions
- Heart Failure, Systolic
- 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 group | Role | What they receive |
|---|---|---|
| Device | Experimental | Participants 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 Care | No intervention | Routine care for heart failure management |
What is being measured
The primary outcome is the main question the study is designed to answer.
GDMT score
Change in GDMT score from between the intervention and control arm.
Measured: 0-90 days
Secondary outcomes (6)
Hospitalized days
Number of days hospitalized between the intervention and control arm
Measured: 0-90 days; 0-180 days
Emergency room visits
Number of emergency room visits between the intervention and control arm
Measured: 0-90 days; 0-180 days
GDMT score
Change in GDMT score from between the intervention and control arm.
Measured: 0-180 days
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
Visual analog score change
Change in visual analog scores from between the intervention and control arm
Measured: day 0-90
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.
- First posted14 Aug 2023
- Study start13 Dec 2024
- Primary completion30 Nov 2025
- Study completion30 Nov 2025
Why it stopped: Due to sponsor request for poor enrollment
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Heart Failure, SystolicStudies of the same condition, open and under way.
- More trials run by University of Texas Southwestern Medical CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- University of Texas Southwestern Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- American Heart Association
- Responsible party
- Principal investigator, Nicholas Hendren, University of Texas Southwestern Medical Center
- Investigators
- Nicholas Hendren, MD, Principal investigator, University of Texas Southwestern Medical Center
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
Study at a glance
From the registry record, last updated by the sponsor on 18 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- American Heart Association Digital Home Remote Monitoring for Heart Failure
- ClinicalTrials.gov ID
- NCT05988749
- Acronym / sponsor ID
- ADHERE-HF / STU-2023-0529
- Conditions
- Heart Failure, Systolic
- Keywords
- remote home monitoring, heart failure, guideline directed medical therapy
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Due to sponsor request for poor enrollment
- Enrolment
- 15 participants (actual)
- Lead sponsor
- University of Texas Southwestern Medical CenterUniversity, hospital or other
- Collaborators
- American Heart Association
- Study start
- 13 Dec 2024 (actual)
- Primary completion
- 30 Nov 2025 (actual)
- Study completion
- 30 Nov 2025 (actual)
- First posted
- 14 Aug 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 2
- 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.
| Arm | Type | Receives |
|---|---|---|
| Device | Experimental | Other: Biofourmis Digital PlatformParticipants 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. |
| Routine Care | No intervention | –Routine care for heart failure management |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- ≥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.
Key exclusion criteria (13 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Biofourmis Digital PlatformAlso: American Heart Association's Digital Heart Failure CarePlans and Education ContentThe 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. | Other | Device |
Primary outcome
GDMT score
Time frame: 0-90 days
Change in GDMT score from between the intervention and control arm.
6 secondary outcomes
Hospitalized days
Time frame: 0-90 days; 0-180 days
Emergency room visits
Time frame: 0-90 days; 0-180 days
GDMT score
Time frame: 0-180 days
Change in KCCQ-12 score
Time frame: day 0-90 and 0-180
Visual analog score change
Time frame: day 0-90
Optimal GDMT dosing
Time frame: 0-90 days, 0-180 days
Results and safety
The study was stopped early (reason given: Due to sponsor request for poor enrollment). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Feb 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Nicholas Hendren, MD principal investigator
University of Texas Southwestern Medical Center
2 sites in 1 country: see every site and its status.
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.