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Clinical Trials/NCT02157285
NCT02157285CompletedNot Applicable

The Influence of Peer Mentoring on Contraceptive Decision Making Among Adolescents

University of Pennsylvania2 sites in 1 country110 target enrollmentStarted: February 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
110
Locations
2
Primary Endpoint
Number of study participants who chose long-acting reversible contraception (LARC) after all contraceptive counseling was done.

Study Overview

Brief Summary

This is a prospective, randomized-controlled trial in which subjects will be randomized to receive either routine contraceptive counseling or peer mentoring plus routine contraceptive counseling.

Detailed Description

Unintended adolescent pregnancy continues to be a significant public health problem in the United States. While the use of highly effective forms of birth control, such as the long-acting, reversible contraceptives (LARC) have been found to be more effective in decreasing pregnancy rates than non-LARC methods of birth control, knowledge and use of LARC has been shown to be low in this vulnerable population. We are interested in better understanding the influence peers may have on contraceptive decision making among adolescents. The purpose of this study is to evaluate the impact of a peer mentoring intervention on adolescent contraceptive decision making, specifically with regard to increasing long-acting, reversible contraceptive uptake. The main study intervention will consist of randomization to usual contraceptive counseling versus peer-mentoring plus usual contraceptive counseling. Pre- and post-intervention questionnaires will be used to better understand peer influence on contraceptive decision making, and to assess the peer mentor-teen intervention interaction.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
13 Years to 21 Years (Child, Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • English speaking
  • Age 13-21 years old at enrollment
  • Desiring contraception; either currently not taking any method of contraception, or not satisfied with current method, and not desiring pregnancy in the next 12 months
  • Willing and able to follow the study protocol

Exclusion Criteria

  • Male gender
  • Younger than 13 years old, older than 21 years old
  • Pregnant or desiring pregnancy within the coming year
  • Issues or concerns in the judgement of the investigator that may compromise the safety of the subject or confound the reliability of compliance and information acquired in this study

Outcomes

Primary Outcomes

Number of study participants who chose long-acting reversible contraception (LARC) after all contraceptive counseling was done.

Time Frame: at enrollment/baseline visit

This data was obtained by the number of participants who chose to have an IUD or Implant inserted after counseling at their clinic visit.

Secondary Outcomes

  • Number of participants who maintained LARC uptake(4 months from enrollment/baseline visit)
  • Number of participants who maintained a positive opinion of LARC method as their primary choice for birth control(4 months after enrollment/baseline visit.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Courtney Schreiber

Director, Fellowship in Family Planning

University of Pennsylvania

Study Sites (2)

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