NCT00361400

Brief Summary

This study is an examination of "high risk" young women, 15-24 years of age, who initiate first time use of vaginal ring, oral contraceptives, contraceptive path, or Depo-provera.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,387

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2005

Typical duration for all trials

Geographic Reach
1 country

5 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2005

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

August 4, 2006

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 8, 2006

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2008

Completed
Last Updated

August 2, 2013

Status Verified

August 1, 2013

Enrollment Period

3.1 years

First QC Date

August 4, 2006

Last Update Submit

August 1, 2013

Conditions

Pregnancy

Keywords

pregnancyhormonal contraception

Eligibility Criteria

Age15 Years - 24 Years
Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Planned Parenthood patients who present to start a hormonal birth control for the first time.

You may qualify if:

  • \- 15-24 years old, English or spanish speaking, Starting ring, pill, patch, or Depo for first time, Sexually active, Single, Not pregnant, Living in Bay Area for next 12 months

You may not qualify if:

  • Past user of method, Married, Pregnant, Moving out of area, Not sexually active

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (5)

Planned Parenthood-Golden Gate

Hayward, California, 94541, United States

Location

Planned Parenthood-Golden Gate

Oakland, California, 94605, United States

Location

Planned Parenthood - Shasta Diablo

Richmond, California, 94806, United States

Location

University of California, San Francisco

San Francisco, California, 94110, United States

Location

Planned Parenthood - Shasta Diablo

Vallejo, California, 94590, United States

Location

Related Links

Biospecimen

Retention: SAMPLES WITHOUT DNA

urine for pregnancy testing

Study Officials

  • Tina R Raine, MD, MPH

    University of California, San Francisco

    PRINCIPAL INVESTIGATOR

  • Cynthia Harper, PhD

    University of California, San Francisco

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 4, 2006

First Posted

August 8, 2006

Study Start

August 1, 2005

Primary Completion

September 1, 2008

Study Completion

September 1, 2008

Last Updated

August 2, 2013

Record last verified: 2013-08

Locations

US(5)