Clinical Trials Directory

Trials / Completed

CompletedNCT03402217

Patient Centered Postpartum Contraception App

Status
Completed
Phase
Study type
Observational
Enrollment
20 (actual)
Sponsor
University of Chicago · Academic / Other
Sex
Female
Age
15 Years – 25 Years
Healthy volunteers
Accepted

Summary

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPatient Centered Postpartum Contraception AppThis is a theory-based smart phone-based application designed to provide immediate postpartum contraception information to young women aged 15-25.

Timeline

Start date
2018-05-18
Primary completion
2019-01-07
Completion
2019-01-07
First posted
2018-01-18
Last updated
2024-05-03
Results posted
2024-05-03

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03402217. Inclusion in this directory is not an endorsement.