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Learning Theory Patient Education for Anticoagulants

Utah System of Higher Education (USHE) logo

Utah System of Higher Education (USHE)

Status

Begins enrollment in 1 month

Conditions

Knowledge, Attitudes, Practice

Treatments

Behavioral: Control Group: Standard of Care
Behavioral: Anticoagulation Educational Materials

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06138184
K23HL157751 (U.S. NIH Grant/Contract)
IRB_00146488

Details and patient eligibility

About

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.

Full description

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.

Enrollment

68 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

68 participants in 2 patient groups

Standard Care
Active Comparator group
Description:
Standard Educational process
Treatment:
Behavioral: Control Group: Standard of Care
Education Intervention
Experimental group
Description:
New educational intervention
Treatment:
Behavioral: Anticoagulation Educational Materials

Trial contacts and locations

0

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Central trial contact

Aubrey E Jones, PharmD, MSCI

Data sourced from clinicaltrials.gov

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