Reducing Adolescent Pregnancy

Children's Hospital of Philadelphia (CHOP)

Status: Completed

Conditions: Counseling; Contraception Behavior; Pregnancy in Adolescence

Treatments: Behavioral: Contraception Counseling

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT04120376

19-016314

5R21HD095096-02 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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).

Full 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.

Enrollment: 144 patients

Sex: Female

Ages: 15 to 18 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. 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.
2. Females who do not desire to become pregnant within the next year.
3. Eligible individuals must be proficient in speaking and reading in English.
4. Consent of the adolescent.

Exclusion criteria

1. Females who are currently using hormonal contraception or an intrauterine device.
2. Females who are pregnant.
3. Patient has a developmental delay limiting participation.
4. Patient is presenting in the ED after sexual assault.
5. Patient is too ill to be screened.

APPs: [no age limit]] Have been working in ED 6 months

Trial design

Primary purpose: Prevention

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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144 participants in 1 patient group

Counseling Intervention

Experimental group

Description:

All participants will receive contraception counseling by study Advanced Practice Providers (APPs)

Treatment:

Behavioral: Contraception Counseling