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Completed

NCT Number: NCT01654991

Randomized Trial of Home Versus Clinic-Based STD Testing

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.

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Key information

Age range

18 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Washington University School of Medicine

St Louis, Missouri, 63110, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

-

Treatment and study plan

Home screening

Behavioral

Home-based STD screening using self-obtained urine samples and study paid postal return of samples.

Clinic screening

Behavioral

Clinic-based STD screening using self-obtained urine samples in a local university clinical setting.

Primary outcomes

  1. Number of men who complete testing in each study arm

    Time frame: 12 weeks after enrollment

Sponsors and collaborators

Lead sponsor

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Nih

Registry information

Official study title

A Randomized Trial of Home Versus Clinic-Based STD Testing Among Men

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
Aug 1, 2012
Registry last updated
Nov 1, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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