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Low Dose Aspirin Alerts in High-Risk Pregnancies

Primary Purpose

Preeclampsia, Aspirin, Clinical Decision Support Systems

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Electronic health record best practice alert
Sponsored by
Geisinger Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Preeclampsia

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Receiving prenatal care within Geisinger Initial prenatal visit prior to 28 weeks gestation Determined to be high risk for preeclampsia based on the modified United States Preventive Services Task Force and American College of Obstetrics and Gynecology criteria (at least 1 high risk factor) Exclusion Criteria: Not pregnant No prenatal visit prior to 28 weeks gestation Maternal-Fetal Medicine only visits Not meeting the modified USPSTF high-risk criteria Contraindication to aspirin, including allergy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    No Intervention

    Arm Label

    Best practice alert (BPA) intervention group

    Standard care group

    Arm Description

    An electronic health record best practice alert (BPA) will alert healthcare providers to recommend low dose aspirin for pregnant patients at high-risk for preeclampsia. This alert also allows the healthcare provider to order an over-the-counter-prescription for low dose aspirin and automatically documents LDA in the patient's medication list.

    Healthcare provider's recommendation for aspirin in patients at high-risk for preeclampsia will be based on current practice (no alerts) and the healthcare provider's knowledge.

    Outcomes

    Primary Outcome Measures

    A sensitivity analysis of the healthcare provider recommendation for low dose aspirin use in patients, specifically those who deliver after 28 weeks
    yes/no

    Secondary Outcome Measures

    The healthcare provider recommendation for low dose aspirin use in all randomized patients
    yes/no

    Full Information

    First Posted
    March 13, 2023
    Last Updated
    June 5, 2023
    Sponsor
    Geisinger Clinic
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05802940
    Brief Title
    Low Dose Aspirin Alerts in High-Risk Pregnancies
    Official Title
    Best Practice Alert (BPA) for Low Dose Aspirin Recommendation in High-risk Pregnancies: a Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    June 19, 2023 (Anticipated)
    Primary Completion Date
    June 19, 2024 (Anticipated)
    Study Completion Date
    June 19, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Geisinger Clinic

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    The goal of this study is to assess the effect of an electronic health record (EHR) clinical decision support tool, also known as a best practice alert (BPA), on healthcare provider recommendations for low dose aspirin use in a high-risk pregnant patient population. The investigators hypothesize that the implementation of the EHR BPA tool will increase the healthcare provider's recommendation for low dose aspirin compared to current standard care.
    Detailed Description
    Low dose aspirin (LDA) has been found to reduce the incidence of preeclampsia in high-risk pregnant patients. At a health system serving central and northeastern Pennsylvania, electronic health record data reveal that clinicians recommend an LDA regimen to only 60% of eligible high-risk pregnant patients, suggesting the need and opportunity for increased LDA recommendation. This study will assess the efficacy of an electronic health record based clinician-facing interruptive clinical decision support tool/best practice alert (BPA) aimed at increasing LDA recommendation for pregnant patients who are at high risk of preeclampsia. Up to 704 patients will be randomized to account for possible 10% miscarriage and early termination rate as we require outcome data on a total of 640 patients for adequate power. Eligible patients will be randomized to a control group, where the clinician receives no BPA, and one experimental group, where the provider receives a BPA noting the patient is at high-risk and recommend the provider order LDA. If LDA is not recommended, there will be a required acknowledgment reason from the provider noting a rationale for not initiating a LDA regimen.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Preeclampsia, Aspirin, Clinical Decision Support Systems, Economics, Behavioral

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigatorOutcomes Assessor
    Masking Description
    We will randomize at level of the patient as to whether or not a BPA will fire when the patient is seen in clinic. Any obstetric care provider who sees a patient that has been randomized to BPA group will receive the alert if indicated. If the alert doesn't fire, the care provider will not be aware as to whether the patient is randomized to the BPA group or whether the alert was not indicated. Clinical investigators and outcomes assessors are blinded.
    Allocation
    Randomized
    Enrollment
    640 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Best practice alert (BPA) intervention group
    Arm Type
    Active Comparator
    Arm Description
    An electronic health record best practice alert (BPA) will alert healthcare providers to recommend low dose aspirin for pregnant patients at high-risk for preeclampsia. This alert also allows the healthcare provider to order an over-the-counter-prescription for low dose aspirin and automatically documents LDA in the patient's medication list.
    Arm Title
    Standard care group
    Arm Type
    No Intervention
    Arm Description
    Healthcare provider's recommendation for aspirin in patients at high-risk for preeclampsia will be based on current practice (no alerts) and the healthcare provider's knowledge.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Electronic health record best practice alert
    Intervention Description
    The electronic health record will identify patients at high-risk for preeclampsia and candidate for low dose aspirin (LDA) prophylaxis. For those in the intervention group, a best practice alert will notify the healthcare provider within the patient's chart during a prenatal visit that LDA should be recommended.
    Primary Outcome Measure Information:
    Title
    A sensitivity analysis of the healthcare provider recommendation for low dose aspirin use in patients, specifically those who deliver after 28 weeks
    Description
    yes/no
    Time Frame
    Assessed between initial prenatal visit and delivery after 28 weeks
    Secondary Outcome Measure Information:
    Title
    The healthcare provider recommendation for low dose aspirin use in all randomized patients
    Description
    yes/no
    Time Frame
    Assessed between initial prenatal visit and delivery
    Other Pre-specified Outcome Measures:
    Title
    Patient taking low dose aspirin
    Description
    yes/no
    Time Frame
    Assessed at time of delivery (>/= 28 weeks)
    Title
    Rate of preeclampsia
    Description
    yes/no
    Time Frame
    Assessed at time of delivery
    Title
    Timing of low dose aspirin recommendation
    Description
    gestational age (weeks)
    Time Frame
    Assessed between initial prenatal visit to delivery (>/= 28 weeks)
    Title
    Timing of low dose aspirin initiation
    Description
    gestational age (weeks)
    Time Frame
    Assessed between initial prenatal visit to delivery (>/= 28 weeks)
    Title
    Preterm delivery
    Description
    yes/no
    Time Frame
    Assessed at delivery
    Title
    Provider response to best practice alert
    Description
    recommended, declined, etc.
    Time Frame
    Assessed between initial prenatal visit to delivery (>/= 28 weeks)
    Title
    Number of times the best practice alert fired for a patient
    Description
    1,2,3,4...
    Time Frame
    Assessed between initial prenatal visit to delivery (>/= 28 weeks)

    10. Eligibility

    Sex
    Female
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Receiving prenatal care within Geisinger Initial prenatal visit prior to 28 weeks gestation Determined to be high risk for preeclampsia based on the modified United States Preventive Services Task Force and American College of Obstetrics and Gynecology criteria (at least 1 high risk factor) Exclusion Criteria: Not pregnant No prenatal visit prior to 28 weeks gestation Maternal-Fetal Medicine only visits Not meeting the modified USPSTF high-risk criteria Contraindication to aspirin, including allergy
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    A. Dhanya Mackeen, MD, MPH
    Phone
    570-714-1099
    Email
    admackeen@geisinger.edu
    First Name & Middle Initial & Last Name or Official Title & Degree
    Amir Goren, PhD
    Phone
    570-214-4395
    Email
    agoren@geisinger.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    A. Dhanya Mackeen, MD, MPH
    Organizational Affiliation
    Geisinger Clinic
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    34581729
    Citation
    US Preventive Services Task Force; Davidson KW, Barry MJ, Mangione CM, Cabana M, Caughey AB, Davis EM, Donahue KE, Doubeni CA, Kubik M, Li L, Ogedegbe G, Pbert L, Silverstein M, Simon MA, Stevermer J, Tseng CW, Wong JB. Aspirin Use to Prevent Preeclampsia and Related Morbidity and Mortality: US Preventive Services Task Force Recommendation Statement. JAMA. 2021 Sep 28;326(12):1186-1191. doi: 10.1001/jama.2021.14781.
    Results Reference
    background
    PubMed Identifier
    29939940
    Citation
    ACOG Committee Opinion No. 743: Low-Dose Aspirin Use During Pregnancy. Obstet Gynecol. 2018 Jul;132(1):e44-e52. doi: 10.1097/AOG.0000000000002708.
    Results Reference
    background

    Learn more about this trial

    Low Dose Aspirin Alerts in High-Risk Pregnancies

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