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Home Screening for Chlamydia Surveillance
This study has been completed.
Sponsors and Collaborators: University of Pittsburgh
Agency for Healthcare Research and Quality (AHRQ)
Information provided by: University of Pittsburgh
ClinicalTrials.gov Identifier: NCT00177437
  Purpose

This is a randomized controlled trial to determine whether a home screening test for chlamydia and gonorrhea will lead to increased use of screening tests and increased detection of sexually transmitted diseases.


Condition Intervention Phase
Chlamydia Trachomatis
Gonorrhea
Behavioral: home testing kit
Phase III

MedlinePlus related topics: Chlamydia Infections Gonorrhea
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Active Control, Single Group Assignment
Official Title: Home Screening for Chlamydia Surveillance

Further study details as provided by University of Pittsburgh:

Primary Outcome Measures:
  • chlamydia and gonorrhea tests completed
  • chlamydia and gonorrhea infections detected

Secondary Outcome Measures:
  • pelvic inflammatory disease cases detected

Estimated Enrollment: 403
Study Start Date: June 1999
Study Completion Date: September 2005
Detailed Description:

This is a phase III randomized controlled trial. We enrolled 403 young women from a variety of clinical settings and neighborhoods in the Pittsburgh, PA region. Women completed a baseline questionnaire and then were randomized to either an intervention group (receive home testing kit every six months) or to a control group (receive a letter suggesting a clinic visit for screening). Participants were followed for 2 years, and medical chart abstraction was done to document tests done in clinical settings. The final study end points were number of tests completed, number of screening tests completed, number of STDs detected, and incident cases of pelvic inflammatory disease.

  Eligibility

Ages Eligible for Study:   15 Years to 29 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria: age 15 to 29, 2 or more risk factors for STDs, sexually active -

Exclusion Criteria: currently pregnant, homeless

-

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00177437

Locations
United States, Pennsylvania
University of Pittsburgh
Pittsburgh, Pennsylvania, United States, 15213
Sponsors and Collaborators
University of Pittsburgh
Investigators
Principal Investigator: Roberta B Ness, MD, MPH University of Pittsburgh
  More Information

Publications indexed to this study:
Study ID Numbers: 0404024
Study First Received: September 12, 2005
Last Updated: December 12, 2007
ClinicalTrials.gov Identifier: NCT00177437  
Health Authority: United States: Institutional Review Board

Study placed in the following topic categories:
Genital Diseases, Female
Bacterial Infections
Sexually Transmitted Diseases
Chlamydia Infections
Gonorrhea
Genital Diseases, Male
Neisseriaceae Infections
Gram-Negative Bacterial Infections

Additional relevant MeSH terms:
Sexually Transmitted Diseases, Bacterial
Chlamydiaceae Infections
Infection

ClinicalTrials.gov processed this record on January 16, 2009