Home Tests |
|
|
Clinical Trial: Providing Birth Control Through Home Health Visits
This study is currently recruiting patients.
|
Purpose
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.
| Condition | Treatment or Intervention |
|---|---|
| Pregnancy | Procedure: Home dispensing of contraception |
MedlinePlus consumer health information
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Effectiveness of Nurse Home Contraceptive Dispensing
Expected Total Enrollment: 600
Study start: June 2003; Expected completion: September 2005
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.
Eligibility
Genders Eligible for Study: Female
Accepts Healthy Volunteers
Criteria
Inclusion Criteria:
- Women of child bearing age
- Not pregnant
- Interested in delaying pregnancy using oral contraceptives or a depo-provera shot
- Had sex in the last month or are planning to have sex in the next month
- Have not used contraception during every sexual encounter within 3 months prior to study entry
Location and Contact Information
Alan L Melnick, MD, MPH 503-494-0756 melnicka@ohsu.edu
Oregon
Clackamas County Public Health Division, Oregon City, Oregon, 97045, United States; Recruiting
Alan L Melnick, MD, MPH, Principal Investigator, Oregon Health & Science University
More Information
Record last reviewed: June 2003
Last Updated: October 13, 2004
Record first received: July 16, 2003
ClinicalTrials.gov Identifier: NCT00065078
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- Home Tests (Lab Tests Online)

Not Signed In -

