N/A
N=20
Patient Centered Postpartum Contraception App
Contraceptive Usage
Bottom Line
View on ClinicalTrials.gov: NCT03402217 ↗Enrolled (actual)
20
Serious AEs
0.0%
Results posted
May 2024
Primary outcome: Primary: Feasibility of Application — 4.47; 4.52; 4.16; 4.26 units on a scale
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Patient Centered Postpartum Contraception App (Behavioral)
- Age
- Pediatric, Adult · 15+ yrs
- Sex
- Female
- Sponsor
- University of Chicago
- Primary completion
- Jan 2019
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Feasibility of Application |
4.47; 4.52; 4.16; 4.26; 3.94; 4.42 | — |
| SECONDARY Prior Method Use |
3; 6; 11; 6; 1; 3 | — |
| SECONDARY Number of Pregnancies (Including Current) |
2 | — |
| SECONDARY Contraception Knowledge |
3.35 | — |
| SECONDARY Patient Activation |
62.0; 62.5 | .383 |
| SECONDARY Information, Motivation and Behavioral Skills |
4.0; 6.0; 20.0; 21.0; 22.0; 23.0 | .001 sig |
| SECONDARY Number of Children |
1 | — |
| SECONDARY Number of Induced Abortions |
— | — |
| SECONDARY Number of Miscarriages |
— | — |
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.
Eligibility Criteria
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
Data sourced from ClinicalTrials.gov (NCT03402217). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.