Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06809686

Study to Collect High-Resolution ECG Data and Patient Insights on Heart Failure Care

An Observational Study to Collect High Resolution 12-Lead Electrocardiogram (ECG) Data for the Development of an ECG Library to Support the Development of a Tool to Monitor Disease Progression, Gather Patient Perspectives on Standard of Care Heart Failure Procedures and Facilitate Familiarity with the Clinical Trial Environment in Patients with Heart Failure with Mildly Reduced or Preserved Ejection Fraction

Status
Recruiting
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Richmond Research Institute · Industry
Sex
All
Age
45 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to establish an electrocardiogram (ECG) data library to facilitate future studies on heart disease. Additionally, the study will be used to monitor changes in the patient's standard of care throughout the study period and gather patient perspectives on routine diagnostic procedures and disease monitoring and feedback on the design of heart failure trials.

Detailed description

Patients with heart failure with mildly reduced or preserved ejection fraction will be invited to participate in this patient observational study. After providing informed consent, participants will then undergo a series of clinical assessments, and the participants' ECGs will be used to contribute to establishing an ECG library for future heart disease research. Additionally, patients' perspectives on the current standard of care clinical procedures will be gathered. Patient preferences will be gathered in relation to factors around routine clinical investigations for heart failure to better design a disease monitoring tool to include clinical and patient preferences. Also, the patients may be updated on the latest therapy options. Additionally, participants may be invited to review and provide feedback on the study design of heart failure trials under development, helping to ensure alignment with patient needs. Their input can identify potential procedure challenges and enhance the clarity of study materials, improving overall patient engagement. A follow-up call with a research physician will provide the opportunity to discuss any issues identified in the clinical baseline assessment and allow the participant to ask any additional questions.

Conditions

Timeline

Start date
2025-02-05
Primary completion
2027-01-21
Completion
2027-02-21
First posted
2025-02-05
Last updated
2025-03-21

Locations

2 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT06809686. Inclusion in this directory is not an endorsement.