Contraception Navigator Program

  • STATUS
    Recruiting
  • End date
    Jan 1, 2026
  • participants needed
    50
  • sponsor
    Indiana University
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Updated on 1 February 2023
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Summary

The goal of this study is to pilot test the IN-Control Birth Control Navigator Program in Central Indiana for use by adolescents who would like to access birth control. The investigators hypothesize that facilitating access to contraception through our intervention will ultimately result in increased feelings of autonomy around these decisions and use of hormonal contraception.

Description

The IN-Control Birth Control Navigator Program will provide personalized attention to adolescents and young adults and will be able to address self-efficacy skills, and abilities through personal interactions with navigator staff and use of targeted services. Importantly, the navigator can assist participants in overcoming specific environmental barriers (transportation, cost, clinical access) and personal barriers (knowledge and confidentiality concerns) before, during and after the clinical encounter.

Details
Condition Contraception, Contraceptive Usage, Health Care Utilization
Age 15years - 19years
Treatment IN-Control (Birth Control Navigator Program)
Clinical Study IdentifierNCT05691270
SponsorIndiana University
Last Modified on1 February 2023

Eligibility

 Yes No Not Sure

Inclusion Criteria

Adolescents between the ages of 15-19yrs
English speaking
Lives within central Indiana couties: Boone, Brown, Hamilton, Hancock, Hendricks, Johnson, Marion, Morgan, Putnam and Shelby (determined by zip code of primary -

Exclusion Criteria

Adolescents younger than 15 or older than 19yrs
Non-English speaking
Lives outside of central Indiana
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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