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Taking people in United KingdomNo phase

Collects heart tracings and patient views in heart failure care

Collects heart electrical recordings and patient feedback in people with heart failure.

Key facts

Who runs it
Richmond Research Institute
Where
London, United KingdomSee the site
Trial code
Registry title
Study to Collect High-Resolution ECG Data and Patient Insights on Heart Failure Care
Status
Recruiting
People taking part
1,000 people, planned
Started
5 Feb 2025
Expected to end
21 Feb 2027
Type of study
Observational
Record updated
20 May 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 45 to 80 who have been diagnosed with heart failure. It collects detailed ECG data and patients' views on heart failure care.

Age
45 to 80 years (inclusive)
Sex
Men and women
Disease stage
Diagnosed with heart failure. The record title names heart failure with mildly reduced or preserved ejection fraction, and test results that do not fit this type exclude a person.

Main reasons for not taking part

  • Positive test for HIV-1 or HIV-2 infection
  • Positive test for Hepatitis B or Hepatitis C infection
  • Mental incapacity, language barriers or unwillingness to follow the study rules, as judged by the Investigator
  • Any condition the Investigator judges to be an undue risk in the trial
  • Test results that do not fit heart failure with mildly reduced or preserved ejection fraction

The registry criteria, word for word

Show all 7 criteriaShow less

Who can take part

  • Male or female participants aged 45 to 80 years (inclusive) at the date of signing the informed consent
  • Diagnosed with heart failure
  • Able and willing to provide informed consent to participate

Who cannot take part

  • Diagnostic test results positive for:; HIV-1 or HIV-2 infection; Hepatitis B or Hepatitis C infection
  • Any condition judged by the Investigator to pose an undue risk while participating in the trial
  • Diagnostic results which are inconsistent with heart failure with mildly reduced or preserved ejection fraction as judged by the Investigator
  • Mental incapacity, language barriers or unwillingness to comply with the requirements of the protocol, which may preclude adequate understanding or cooperation during the study as judged by the Investigator

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 45 and 80 years old?

Where in United Kingdom

  • Richmond PharmacologyLondon, United KingdomContact: Volunteer Recruitment TeamTaking people

About the trial

What the trial wants to find out

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.

The group in the trial

  • Patients with Heart Failure with Mildly Reduced or Preserved Ejection Fraction

    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

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
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
Plain-language title
Collects heart tracings and patient views in heart failure careGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Fit questions
Built from NCT06809686, who can take part
Record updated
20 May 2026