Viewing Study NCT00065078



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Last Modification Date: 2024-10-26 @ 9:09 AM
Study NCT ID: NCT00065078
Status: UNKNOWN
Last Update Posted: 2005-09-13
First Post: 2003-07-16

Brief Title: Providing Birth Control Through Home Health Visits
Sponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development NICHD
Organization: Eunice Kennedy Shriver National Institute of Child Health and Human Development NICHD

Study Overview

Official Title: Effectiveness of Nurse Home Contraceptive Dispensing
Status: UNKNOWN
Status Verified Date: 2005-09
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study will evaluate a program that provides birth control to low income and minority women through home visits by a community health nurse The goal of the program is to reduce unwanted pregnancies
Detailed Description: Unintended pregnancy is associated with significant public health problems including inadequate prenatal care low birth weight infants infant mortality and maternal morbidity and mortality Children born as a result of unplanned pregnancies are at greater risk for poor outcomes such as poor mental health and developmental disabilities This research project will determine whether providing contraception in the home can reduce the incidence of unintended pregnancy in low income and minority women The project will also determine whether delaying a pelvic exam encourages or discourages the utilization of clinic-based preventive services to screen for sexually transmitted diseases STDs and cervical cancer

Participants will be randomized to either an experimental group or a comparison group Each participant will receive family planning counseling during a home visit by a community health nurse Participants in the experimental group will be offered a three-month supply of oral contraceptives or a depo-provera shot both forms of contraceptives will be delivered during home visits Each participant will complete a survey during the initial visit and during a 1-year follow-up The study will last approximately three years

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None