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

ConditionPostpartum
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorNorthwestern University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Postpartum women

Nulliparity

Age >18 years of age

English speaking patients

Disqualifiers

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)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Participant will view a visual aid picture (appendix A) first

    Other intervention

    Participant will view a visual aid picture (appendix A) of a post delivery complication first

  • Participant will view a visual aid picture (appendix B) first

    Other intervention

    Participant will view a visual aid picture (appendix B) of a post delivery complication first

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Participant will view a visual aid picture (appendix A) firstOther 1 intervention
Group B: Participant will view a visual aid picture (appendix B) firstOther 1 intervention

Trial outcomes

Primary outcomes

1

Number of participants who recognize deep vein thrombosis,

Participant will accurately identify the health care issue shown to participants and identified as Picture A and Picture B

Time frame
1 Day

Secondary outcomes

1

Number of participants who demonstrate understanding deep vein thrombosis,

Participants written response of the understanding of deep vein thrombosis.

Time frame
1 Day
2

Number of participants who would report deep vein thrombosis

After review of Picture A and Picture B number of participants who report deep vein thrombosis to their care provider or emergency room.

Time frame
1 Day

Other outcomes

Sponsors and contacts

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