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Navigating the Grey Zone for Antenatal Corticosteroids

University of British Columbia logo

University of British Columbia

Status

Unknown

Conditions

Decision Making, Shared
Preterm Birth
Pregnancy

Treatments

Behavioral: Decision support tool

Study type

Interventional

Funder types

Other

Identifiers

NCT04792112
H20-03071

Details and patient eligibility

About

The purpose of this study is to find out if including a decision support tool in clinical practice guidelines will improve how doctors discuss the option of antenatal corticosteroid treatment with patients who might deliver at 34 to 36 weeks of pregnancy.

Enrollment

460 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 year or older.
  • Delivered a live neonate at 34+0 to 36+6 weeks of gestation.
  • Speaks English.
  • Agrees to participate in the questionnaire during their first week post-partum.
  • Delivered at one of the six participating obstetrical hospitals.

Exclusion criteria

  • None.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

460 participants in 2 patient groups

Guideline + decision support tool
Experimental group
Description:
A decision support tool summarizing harms and benefits of late preterm antenatal corticosteroids will be integrated into the clinical practice guideline available to clinicians in the hospitals in the experimental arm.
Treatment:
Behavioral: Decision support tool
Guideline only
No Intervention group
Description:
Clinicians in the hospitals in the 'no-intervention' arm will have access to the standard guideline only (without the integrated decision support tool).

Trial contacts and locations

2

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Central trial contact

Jessica Liauw, MD

Data sourced from clinicaltrials.gov

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