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NCT05032495 Clinical Trial

Patient Engagement Study to Evaluate the Use of Biological Therapies for Cardiac Arrhythmias

Arrythmia Clinical Trial

Official title:
Patient Directed Strategies for Cardiac Arrhythmia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05032495
Other study ID # 3174
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2022
Est. completion date August 31, 2023

Study information
Verified date April 2024
Source Ottawa Heart Institute Research Corporation
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

In this patient engagement study, patients and partners will attend a presentation, group meeting and responding to the survey to help the research team gage the acceptability of using a biological therapy to prevent cardiac arrhythmia. Patient Partners will also help to clarify which outcomes are important to patients, to ensure the selected outcomes align with patient interests.

Description:

There will be four study groups: 1. Heart patients who experienced a cardiac arrhythmia while in hospital, 2. Heart patients who did not experience a cardiac arrhythmia while in hospital, 3. Heart patients with an upcoming procedure that have not had a cardiac arrhythmia, 4. Members of the general public. There will be a presentation, two surveys and a team meeting. Results will be compiled and analyzed.

Recruitment information / eligibility
Status Completed
Enrollment 22
Est. completion date August 31, 2023
Est. primary completion date August 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion criteria: - Upcoming or previous cardiac procedure. Exclusion Criteria: - Inability to complete an electronic survey or participate in a small group meeting.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Surveys
Surveys to evaluate prior experience, opinions and intervention acceptability.
• Focus group
To answer any questions and discuss topics covered in the standard presentation.

Locations
Country Name City State
Canada University of Ottawa Heart Insitute Ottawa Ontario

Sponsors (1)
Lead Sponsor Collaborator
Ottawa Heart Institute Research Corporation

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of participants that would accept a biological therapy for a cardiac arrhythmia as assessed using a survey accept a biological therapy 2 years
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