Fact CheckerSign in

NCT05906745Completed

Guideline Directed Medical Therapy (GDMT) Optimization and Adherence Longitudinal Study for Heart Failure.

Guideline Directed Medical Therapy (GDMT) Optimization and Adherence Longitudinal Study for Heart Failure. (GOALS-HF)

Source: ClinicalTrials.gov · Last updated 19 Feb 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Observational
Enrollment
52 (actual)
First submitted
30 May 2023
Start date
21 Jul 2023
Primary completion date
27 Sept 2024
Lead sponsor
Tricog Health Inc
NCT number
NCT05906745

What you commit to

  • Study type: Observational
  • Participants enrolled: 52
  • From 21 Jul 2023 to the primary completion date, 27 Sept 2024
  • 4 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current or anticipated use of home intravenous inotrope therapy.
  • Planned (within next 6 months) surgery

Other illness

  • Under consideration for or recipient of advanced heart failure therapies (LVAD, Transplant)

Other

  • 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
  • Inability to provide written consent

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Manipal Hospital
Coordinator of this site? Confirm its status
BengaluruIndiaUnknown status
Sakra World Hospital
Coordinator of this site? Confirm its status
BengaluruIndiaUnknown status
UT Southwestern Medical Center
Coordinator of this site? Confirm its status
DallasUnited StatesUnknown status
Duke University Medical Center
Coordinator of this site? Confirm its status
DurhamUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.