Learning Theory Patient Education for Anticoagulants

NCT ID: NCT06138184

Last Updated: 2025-12-17

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

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-04-30

Study Completion Date

2026-12-31

Brief Summary

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The goal of this study is to test the feasibility of a randomized control trial evaluating the educational tool for anticoagulated patients.

Participants will be randomized to use new educational materials or current existing educational materials and answer survey questions.

Detailed Description

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Eligible patients will be randomized using stratified block randomization to control for the type of anticoagulant (warfarin vs. DOAC) and status (naïve vs. experienced) to either the education intervention from Aim 2 or standard of care Data will be collected via online surveys before the intervention, immediately after, and then 3 months after the intervention.

Patients at the University of Utah Thrombosis Clinic will be recruited.

Conditions

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Knowledge, Attitudes, Practice

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Standard Care

Standard Educational process

Group Type ACTIVE_COMPARATOR

Control Group: Standard of Care

Intervention Type BEHAVIORAL

This will be the current practice for patient education

Education Intervention

New educational intervention

Group Type EXPERIMENTAL

Anticoagulation Educational Materials

Intervention Type BEHAVIORAL

This includes new web-based patient educational materials that have been developed prior to the start of the study

Interventions

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Anticoagulation Educational Materials

This includes new web-based patient educational materials that have been developed prior to the start of the study

Intervention Type BEHAVIORAL

Control Group: Standard of Care

This will be the current practice for patient education

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* initiating (naïve) or currently taking (experienced) oral anticoagulants with an anticipated treatment duration of at least three months
* Experienced patients will be eligible if they score less than 75% on the Anticoagulation Knowledge Test

Exclusion Criteria

* Deficits in cognitive abilities, sensory input, or language significant enough to impede their use of the education tool and/or provision of written informed consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Heart, Lung, and Blood Institute (NHLBI)

NIH

Sponsor Role collaborator

University of Utah

OTHER

Sponsor Role lead

Responsible Party

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Aubrey E. Jones

Assistant Research Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Aubrey E Jones, PharmD, MSCI

Role: PRINCIPAL_INVESTIGATOR

University of Utah

Central Contacts

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Aubrey E Jones, PharmD, MSCI

Role: CONTACT

801-587-9715

Other Identifiers

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K23HL157751

Identifier Type: NIH

Identifier Source: secondary_id

View Link

IRB_00146488

Identifier Type: -

Identifier Source: org_study_id