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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03744936
Other study ID # 18-007275
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 4, 2018
Est. completion date February 6, 2020

Study information

Verified date November 2021
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assist patients and clinicians to reach SDM about treatment options for patients with nonvalvular chronic Atrial Fibrillation screening the investigators aim to develop an evidence-based decision aid for use before the clinical encounters. Our goal is to promote evidence-based patient-centered care. Ideally, this care should reflect the research evidence about anticoagulation treatment. It should also reflect the values and preferences of the informed patient.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date February 6, 2020
Est. primary completion date February 6, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 1. Must be 18 or older 2. Must have an appointment for Atrial Fibrillation 3. Must not have dementia 4. Must not have severe hearing or vision impairment Patients will be given a written consent Guests that accompany patients will be given an oral consent KER unit PAG members will be given an oral consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
DA4Afib Prototyping
We will develop a prototype from patients with atrial fibrillation

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Decisional Conflict Decisional conflict will be measured using the decisional conflict scale Immediatly following clinical visit
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