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

NCT ID: NCT05032495

Last Updated: 2024-04-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

22 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-05-01

Study Completion Date

2023-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Arrythmia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Heart patients who experienced a cardiac arrhythmia while in hospital

Heart patients who experienced a cardiac arrhythmia while in hospital

Surveys

Intervention Type OTHER

Surveys to evaluate prior experience, opinions and intervention acceptability.

Focus group

Intervention Type OTHER

To answer any questions and discuss topics covered in the standard presentation.

Heart patients who did not experience a cardiac arrhythmia while in hospital

Heart patients who did not experience a cardiac arrhythmia while in hospital

Surveys

Intervention Type OTHER

Surveys to evaluate prior experience, opinions and intervention acceptability.

Focus group

Intervention Type OTHER

To answer any questions and discuss topics covered in the standard presentation.

Heart patients with an upcoming procedure that have not had a cardiac arrhythmia

Heart patients with an upcoming procedure that have not had a cardiac arrhythmia

Surveys

Intervention Type OTHER

Surveys to evaluate prior experience, opinions and intervention acceptability.

Focus group

Intervention Type OTHER

To answer any questions and discuss topics covered in the standard presentation.

Members of the general public

Members of the general public

Surveys

Intervention Type OTHER

Surveys to evaluate prior experience, opinions and intervention acceptability.

Focus group

Intervention Type OTHER

To answer any questions and discuss topics covered in the standard presentation.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Surveys

Surveys to evaluate prior experience, opinions and intervention acceptability.

Intervention Type OTHER

Focus group

To answer any questions and discuss topics covered in the standard presentation.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Upcoming or previous cardiac procedure.

Exclusion Criteria

* Inability to complete an electronic survey or participate in a small group meeting.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ottawa Heart Institute Research Corporation

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Darryl Davis

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Darryl Davis

Role: PRINCIPAL_INVESTIGATOR

Ottawa Heart Institute Research Corporation

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Ottawa Heart Insitute

Ottawa, Ontario, Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

References

Explore related publications, articles, or registry entries linked to this study.

Smith C, Lalu MM, Davis DR. Exploring Patient Viewpoints to Optimize Implementation of a Biological Therapy for Atrial Fibrillation Prevention. CJC Open. 2024 Apr 16;6(7):893-900. doi: 10.1016/j.cjco.2024.04.003. eCollection 2024 Jul.

Reference Type DERIVED
PMID: 39026620 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

3174

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Ventricular Tachycardia Mechanisms
NCT05478213 RECRUITING NA