Barriers to Referring Adolescent Women for Etonogestrel Implant.

Status Withdrawn

Clinical Trial Summary

This study seeks to understand how much pediatric providers in Central Florida know about the etonogestrel contraceptive implant. The investigators also seek to understand the barriers that may prevent them from referring adolescent women for this highly effective and recommended method of contraception. Finally the study will consider if an expanded education and coaching improves their ability to referring patients for this method of birth control.

Clinical Trial Description

This study is comprised of two phases. During the first phase 500 medical providers who provide care to adolescents will be recruited to complete a 30 question anonymous survey that evaluates their attitudes towards recommending and referring for adolescent women for the etonogestrel contraceptive device. This survey will also test participant's knowledge of indications, side effects and side effect management related to this contraceptive device as well. During phase 2, 100 pediatric providers will be randomized to two groups. One group will receive standard continuing medical education on the use of the etonogestrel device in adolescents focusing on themes that emerged as knowledge deficits in phase 1. The other group will receive standard continuing medical education plus continued coaching on management of medication side effects. The referring patterns of physicians in each group will be studied. ;

Study Design

Related Conditions & MeSH terms

Contraceptive Usage

Clinical Trial Details

NCT number	NCT04882137
Study type	Interventional
Source	Nemours Children's Clinic
Contact
Status	Withdrawn
Phase	N/A
Start date	September 1, 2023
Completion date	June 30, 2024

View Details

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