N/A
N=13
Providing Adolescent Contraception in the Emergency Room
Contraception
Bottom Line
View on ClinicalTrials.gov: NCT02475980 ↗Enrolled (actual)
13
Serious AEs
0.0%
Results posted
Jul 2016
Primary outcome: Primary: Length of Stay — 287 minutes
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Comprehensive contraception counseling (Behavioral)
- Age
- Pediatric, Adult · 13+ yrs
- Sex
- Female
- Sponsor
- University of New Mexico
- Primary completion
- Jul 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Length of Stay |
287 | — |
| PRIMARY Proportion of Eligible Girls Offered Counseling Intervention |
13 | — |
| PRIMARY Participant Satisfaction |
4; 3; 1; 0; 0 | — |
| PRIMARY Contraceptive Initiation |
1 | — |
| SECONDARY Descriptive Statistics of Participants |
2; 1; 2; 5 | — |
| SECONDARY Follow-up Adherence |
3; 2; 0 | — |
Summary
The purpose of this pilot study is to determine the feasibility of comprehensive contraceptive counseling intervention in a pediatric emergency department and to determine the impact of comprehensive contraception counseling on initiation of contraception among sexually active adolescents presenting to a pediatric emergency department.
Eligibility Criteria
Inclusion Criteria
- Ages 13 to 18 years old
- Speaks English or Spanish
- Has menstrual periods
- Has Medicaid insurance
Exclusion Criteria
- Seeking contraception as their primary complaint
- Currently pregnant based on urine or serum pregnancy testing
- Has an IUD or contraceptive implant (Implanon/Nexplanon)
- Critically ill, hemodynamically unstable, altered mental status, developmentally delayed, severe pain or distress, or have major trauma
- In juvenile justice custody
Data sourced from ClinicalTrials.gov (NCT02475980). 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.