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Novel Visual Education Tool to Improve Recognition and Reporting of Postpartum Urgent Maternal Warning Signs

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Northwestern University

Status

Enrolling

Conditions

Postpartum

Treatments

Other: Participant will view a visual aid picture (appendix B) first
Other: Participant will view a visual aid picture (appendix A) first

Study type

Interventional

Funder types

Other

Identifiers

NCT06912776
STU00222375

Details and patient eligibility

About

This study aims to create a novel visual education tool that builds on the urgent maternal warning signs identified by The Council on Patient Safety in Women's Health Care. Including effective images will improve the understanding of these grave warning signs/symptoms, improving anatomical accuracy while remaining simplistic for patients of varying levels of health care literacy. The investigative team will be focusing on urgent warning signs pertinent to the postpartum period.

Enrollment

40 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Postpartum women
  • Nulliparity
  • Age >18 years of age
  • English speaking patients

Exclusion criteria

  • Inability to provide informed written consent
  • Refusal to participate in all study-related procedures
  • Patients not fluent in English
  • Patients with current or history of serious peripartum complications and/or events - such as DVT, PE, peripartum cardiomyopathy, etc. (in which the patient may have received more than standard clinical counseling)
  • Patient with comorbidities that potentially require anticoagulation i.e. coagulopathies and may be more prone to DVTs
  • Patients with uncorrected visual or hearing impairment
  • Healthcare providers (in which patients will have significant background knowledge)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Participant will view a visual aid picture (appendix A) first
Other group
Description:
Participant will view a visual aid picture (appendix A) of a post delivery complication first.
Treatment:
Other: Participant will view a visual aid picture (appendix A) first
Participant will view a visual aid picture (appendix B) first
Other group
Description:
Participant will view a visual aid picture (appendix B) of a post delivery complication first
Treatment:
Other: Participant will view a visual aid picture (appendix B) first

Trial contacts and locations

1

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Central trial contact

Paul C Fitzgerald, RN,BSN,MS

Data sourced from clinicaltrials.gov

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