Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

San Francisco, California 94118


Purpose:

The purpose of the study is to measure whether an education and training intervention for clinicians and contraceptive counselors on long-acting reversible contraception (LARC) will result in greater use of the methods among contraceptive patients.


Study summary:

Unintended pregnancy is extremely high in the United States among young women, and use of contraceptives with top-tier effectiveness, intrauterine contraception and implants, is low. Contraceptive providers in the US have low knowledge of current scientific evidence on LARC methods, and do not routinely include these methods in counseling patients at highest risk of unintended pregnancy. This intervention provides evidence-based education and hands-on training to clinicians and contraceptive educators in Planned Parenthood affiliated Title X clinics throughout the US on LARC methods.


Criteria:

Inclusion Criteria: This study involves two groups of human subjects: patients and staff at participating Planned Parenthood (PP) clinics in the United States. Patient participants are young women receiving contraceptive counseling at Planned Parenthood clinics and staff participants are the clinicians and health educators serving these women. Patients must be: Female; - Age 18-25; - Fluent in English or Spanish; - Not wanting to become pregnant in the next 12 months; - Sexually active in past 3 months; - At risk of pregnancy; - Received contraceptive counseling; - Not pregnant; - Willing to be contacted by telephone over the next 12 months. Clinic staff must be: - Employed by a participating PP clinic; and - Offer clinical care, counseling or education for abortion or contraception at the clinic. (This may include physicians, advance practice clinicians, nurses, social workers and health educators.) For clinics to be eligible to be study sites, they must: - Not share staff - Have no active LARC interventions ongoing - Have >400 clients/year


NCT ID:

NCT01360216


Primary Contact:

Principal Investigator
Cynthia C Harper, PhD
University of California San Francisco School of Medicine


Backup Contact:

N/A


Location Contact:

San Francisco, California 94118
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.