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Randomized Trial of Home Versus Clinic-Based STD Testing

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Jeffrey Peipert, Washington University School of Medicine
ClinicalTrials.gov Identifier:
NCT01654991
First received: July 29, 2012
Last updated: NA
Last verified: June 2011
History: No changes posted

July 29, 2012
July 29, 2012
June 2010
December 2011   (final data collection date for primary outcome measure)
Number of men who complete testing in each study arm [ Time Frame: 12 weeks after enrollment ] [ Designated as safety issue: No ]
Same as current
No Changes Posted
 
 
 
 
 
Randomized Trial of Home Versus Clinic-Based STD Testing
A Randomized Trial of Home Versus Clinic-Based STD Testing Among Men

This study randomizes St. Louis men to home-based STD screening or clinic-based STD screening. Home-based screening will be completed through the mail and clinic-based screening in a local clinical setting. We hypothesize that men randomized to home-based screening will be more likely to complete screening.
 
Interventional
 
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Screening
  • Chlamydia
  • Gonorrhea
  • Behavioral: Home Screening
    Home-based STD screening using self-obtained urine samples and study paid postal return of samples.
  • Behavioral: Clinic Screening
    Clinic-based STD screening using self-obtained urine samples in a local university clinical setting.
  • Active Comparator: Clinic-Based Testing
    Clinic-based STD screening using self-obtained urine samples in a local university clinical setting.
    Intervention: Behavioral: Clinic Screening
  • Experimental: Home-Based Testing
    Home-based STD screening using self-obtained urine samples and study paid postal return of samples.
    Intervention: Behavioral: Home Screening
 

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
200
December 2011
December 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Men
  • Ages 18-45
  • Residing in St. Louis City or County
  • English-speaking

Exclusion Criteria:

-
Male
18 Years to 45 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01654991
201105031
No
Jeffrey Peipert, Washington University School of Medicine
Washington University School of Medicine
 
Principal Investigator: Jeffrey F Peipert, MD, PhD Washington University School of Medicine
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
June 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP