Guideline Directed Medical Therapy (GDMT) Optimization and Adherence Longitudinal Study for Heart Failure.
Completed
Conditions studied: Heart Failure
In brief
A multicenter, non-randomized prospective longitudinal study to evaluate the feasibility of Tricog's Remote platform for Guideline Directed Medical Therapy (GDMT) titration and remote patient monitoring among patients with Heart Failure.
Key facts
- Study ID
- NCT05906745
- Run by
- Tricog Health Inc
- People needed
- 52
- Starts
- 2023-07-21
- Expected to finish
- 2024-09-27
- Last updated by the study team
- 2025-02-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 years
- Recent hospitalization (within 4 weeks of enrollment) for HF with IV diuretic use
- Echocardiographic data with EF measurements available in the last 6 months and after HF diagnosis
- Established outpatient care at the participating sites
- Eligible to receive at least 2 of the 4 GDMT classes (ACEi/ARB/ARNi, Beta-blockers, MRA, and SGLT2i) for HFrEF and HFmrEF and at least one of the three (ARB/ARNI, MRA, SGLT2i) for HFpEF
- Not on Target GDMT for all the eligible GDMT classes
- >12 months of expected survival
- Comfortable with spoken and written English communication
- Access to Apple Watch-compatible iPhone
You may not qualify if…
- Under consideration for or recipient of advanced heart failure therapies (LVAD, Transplant)
- Current or anticipated use of home intravenous inotrope therapy.
- Unwilling or unable to perform all study related procedures (wear watch, take measurements and maintain daily logs)
- Post-discharge placement in nursing, rehabilitation, or long-term care facility
- Planned (within next 6 months) surgery
- Inability to provide written consent
Where it is running
- Duke University Medical Center — Durham, North Carolina, United States
- UT Southwestern Medical Center — Dallas, Texas, United States
- Manipal Hospital — Bengaluru, Karnataka, India
- Sakra World Hospital — Bengaluru, Karnataka, India
Full record on ClinicalTrials.gov
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