Reducing Adolescent Pregnancy
- Conditions
- Pregnancy in AdolescenceContraception BehaviorCounseling
- Interventions
- Behavioral: Contraception Counseling
- Registration Number
- NCT04120376
- Lead Sponsor
- Children's Hospital of Philadelphia
- Brief Summary
This multi-site study is employing a brief contraception counseling intervention in the Emergency Department (ED) to shed light on factors that affect decision making as well as barriers and facilitators to conception initiation in the Emergency Department (ED) setting. The overarching goal of the study is to reduce unintended pregnancy among females ages 15 to 18 who present to the Emergency Department (ED).
- Detailed Description
This study is a prospective cohort study involving females who present to one of two emergency departments (ED) between the ages of 16 and 18, who are at risk of unintended pregnancy.
Our primary objective is to assess intention to initiate contraception ("high"=very/somewhat likely vs "low"=unsure/not likely/definitely not on Likert scale survey) among females aged 15 to 18 years who receive emergency department-based contraceptive counseling.
Our secondary objectives are as follows:
1. Among the same population, assess completion of a referral for any contraceptive care, defined as attendance at a referral site within 4 weeks after the index ED visit.
2. Assess the proportion who ultimately initiate contraception through electronic medical record documentation (i.e., visit note, procedure note, medication review) and participant report (follow-up calls).
3. Use qualitative interview methodology to explore attitudes, barriers, and facilitators that affect decisions to A) express intention to initiate contraception, B) complete a referral for contraceptive care, and C) ultimately initiate contraception among this unique group of high-risk adolescents.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 144
- Females aged 15-18 years who are at high-risk of pregnancy, defined as sexual activity within the last 6 months or likely future sexual activity.
- Females who do not desire to become pregnant within the next year.
- Eligible individuals must be proficient in speaking and reading in English.
- Consent of the adolescent.
- Females who are currently using hormonal contraception or an intrauterine device.
- Females who are pregnant.
- Patient has a developmental delay limiting participation.
- Patient is presenting in the ED after sexual assault.
- Patient is too ill to be screened.
APPs: [no age limit]] Have been working in ED 6 months
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Counseling Intervention Contraception Counseling All participants will receive contraception counseling by study Advanced Practice Providers (APPs)
- Primary Outcome Measures
Name Time Method Intention to Initiate Contraception up to 8 weeks Intention to initiate contraception at Emergency Department (ED) or follow-up visit from survey responses
- Secondary Outcome Measures
Name Time Method Contraceptive Care Referral Completion up to 8 weeks Participants completed a referral visit for any contraception care
Initiation of Contraception up to 12 weeks Participant has started contraception as evidenced by electronic medical record view and follow-up phone calls or surveys
Trial Locations
- Locations (2)
Children's Mercy Hospital
🇺🇸Kansas City, Missouri, United States
Children's Hospital of Philadelphia
🇺🇸Philadelphia, Pennsylvania, United States