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Completed

NCT Number: NCT02157285

Influence of Peer Mentoring on Adolescent Contraceptive Decision Making

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.

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Key information

Age range

13 year–21 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Pennsylvania

Philadelphia, Pennsylvania, 19104, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • English speaking
  • Female
  • 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

Treatment and study plan

Peer Mentor Counseling

Behavioral

Peer mentoring will entail the peer mentor describing her positive experience with her LARC method. The participant will then have a chance to ask any experience related questions to the mentor. Any clinical inquiries or questions the mentor does not feel comfortable answering, she will defer to the contraceptive counselor/ physician who will be subsequently providing the routine counseling. The entire peer mentor encounter should not last more than 10 minutes.

Primary outcomes

  1. 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

  1. Number of participants who maintained LARC uptake

    Time frame: 4 months from enrollment/baseline visit

    This data is being obtained through a brief follow-up questionnaire conducted over the phone.

  2. Number of participants who maintained a positive opinion of LARC method as their primary choice for birth control

    Time frame: 4 months after enrollment/baseline visit.

    This data is being obtained through a brief follow-up questionnaire conducted over the phone.

Sponsors and collaborators

Lead sponsor

University of Pennsylvania

Other

Registry information

Official study title

The Influence of Peer Mentoring on Contraceptive Decision Making Among Adolescents

Acronym: ImPACCT

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Jun 5, 2014
Registry last updated
Jun 6, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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