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Patient Centered Postpartum Contraception App

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The University of Chicago

Status

Completed

Conditions

Contraceptive Usage

Treatments

Behavioral: Patient Centered Postpartum Contraception App

Study type

Observational

Funder types

Other

Identifiers

NCT03402217
IRB17-12541

Details and patient eligibility

About

This study will evaluate a smart phone-based application ("app") designed to inform pregnant women ages 15-25 about their contraception options. The goal of this research will be to evaluate the usability, feasibility and acceptability of this app.

Full description

This study will evaluate a smart phone-based application ("app") designed to inform pregnant women ages 15-25 about their contraception options. The goal of this research will be to evaluate the usability, feasibility and acceptability of this app. Participants will be asked to complete a survey after informed consent and before using the app. After using the app, participants will complete a second survey. This second survey will ask questions about the app including the following topics: Usability, user-friendliness, navigation, user interface, time spent, organization readability; Feasibility, informative, helpful, comprehensible, quality of art, interface, sound; and Acceptability breadth of content, depth of content, engaging and motivating, Innovative utility and value. Women will also rate the degree to which they promote use of the product: would use the app if available, believe the app will support contraceptive use and would recommend the app to peers. Study participation will end once participants are done with the second survey.

Enrollment

20 patients

Sex

Female

Ages

15 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Pregnant
  • Identify as African American or Black
  • English as primary language

Exclusion criteria

  • Not pregnant
  • Not identifying as African American or Black
  • Language other than English as primary language

Trial design

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Brandon Hill, PhD; Jennifer Rowley, MS(c)

Data sourced from clinicaltrials.gov

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